program jp

130
  1   94 プログラム アドバンスト・テクノロジー・プログラム (ATP)P. 7 アカデミックプログラム (AP)P. 13 となります S1  カンファレンスホール 未来をきり330  131014004S  21 する ~ナノカーボン ~(13:1014:00  140014504S 2    -(14:0014:50 井上  150015504S 3  がもたらすロセス深津15:0015:50 井上 155016404S 4  らせようーの「くすり」がア フリカにー 15:5016:40S2  シンポジオンホール 327  11001200 S2   47 かした岡山11:0012:00327 13001400 S2  2  および センター 13:0014:00  14301530 S2  3  ラジカル西14:3015:30彰式 32813401520ページをごさい。 329  130014003S2   クラスターをとした 13:0014:00  143015303S2  2  ナノカーボンをとするπ 14:3015:30S3  1  121のためのによるアプローチ 327  13301430 S3   らかさをしたタンパクとその13:3014:00 S3  2  におけるらかさの 14:0014:30  14301530 S3  3  QM/MM によるエネルギー14:3015:00 S3  4  シミュレーションによる内光 エネルギー 15:00 15:30  16001730 S3  5  らかさとシミュレーショ ンによるアプローチ 16:0016:30 S3  6  みだす -ダイナミックス-岡山松本16:3017:00 S3  7  討論17:0017:30S4  1  131エレクトロニクスのパラダイムとするデバイスの32713301335 S4   13:3013:35  13351510 S4  2  ナノシートの西 13:3514:10 S4  3  シリセンπするモノレイヤーケ シートのマテリアル14:1014:45 S4  4  グラフェンのおよびデバイスへの中一14:4515:10 田15201705 S4  5  ナノカーボン・単原とそ エネ15:2015:55 S4  6  エレクトロニクスしたラフェンの15:5516:30 S4  7  グラフェンとカーボンナノチューブをしたリチウムエネルギー  16:3017:05

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  • 1

    94

    (ATP) P. 7

    (AP) P. 13

    S1

    330

    131014004S1-01 21 13:1014:00

    140014504S1-02 14:0014:50

    150015504S1-03 15:0015:50

    155016404S1-04 15:5016:40

    S2

    327

    110012001S2-01 4711:0012:00

    327 13001400

    1S2-02 13:0014:00

    143015301S2-03 14:3015:30

    328

    13401520

    329

    130014003S2-01 13:0014:00

    143015303S2-02 14:3015:30

    S3 1 121

    327

    133014301S3-01 13:3014:00

    1S3-02 14:0014:30

    143015301S3-03 QM/MM14:3015:00

    1S3-04 15:0015:30

    160017301S3-05 16:0016:30

    1S3-06 --16:3017:00

    1S3-07 17:0017:30

    S4 1 131

    327

    133013351S4-01 13:3013:35

    133515101S4-02 13:3514:10

    1S4-03 14:1014:45

    1S4-04 14:4515:10

    152017051S4-05 15:2015:55

    1S4-06 15:5516:30

    1S4-07 16:3017:05

  • 2

    S5 1

    - II

    327

    900 10201S5-01 09:0009:05

    1S5-02 FIBER09:0509:30

    1S5-03 JST 09:3009:55

    1S5-04 RNA09:5510:20

    102011201S5-05 10:2010:50

    1S5-06 10:5011:20

    112012301S5-07 11:2011:50

    1S5-08 In Vivo JSTCREST11:5012:20

    1S5-09 12:2012:30

    2014

    327

    13301730

    329

    900 1210

    329

    13301730

    330

    133013554S5-01 13:3013:35

    4S5-02 13:3513:55

    135514454S5-03 Exciting New Enzymes From Fungal BiosyntheticPathwaysUin. of California, Los AngelesYI, Tang13:5514:25

    4S5-04 14:2514:45

    144515354S5-05 Semi-synthetic artemisinin: Using synthetic biologyto increase the supply of a crucial antimalarial drugAmyris, Inc.MICHAEL, Leavell14:4515:15

    4S5-06 15:1515:35

    153516154S5-07 15:3515:55

    4S5-08 15:5516:15

    S6 2

    - 2014-

    327

    930 940 1S6-01 09:3009:40

    940 10301S6-02 JASRI 09:4010:00

    1S6-03 10010:0010:30

    103011301S6-04 10:3011:00

    1S6-05 11:0011:30

    113012001S6-06 BiNiO3 11:3012:00

    327

    133015001S6-07 13:3013:40

    1S6-08 13:4014:00

    1S6-09 14:0014:20

    1S6-10 14:2014:40

    1S6-11 Pillar[n]arene14:4015:00

    151016301S6-12 15:1015:30

    1S6-13 ALCA, JST 15:3015:50

    1S6-14 Photochemical Organocatalytic ReactionsICIQ,Institute of Chemical Research of Catalonia, SpainMELCHIORRE, Paolo15:5016:30

    328

    900 1110

    The Chemical Record Lecture 2014

    328

    15301620

  • 3

    8

    329

    13301715

    330

    930 10304S6-01 09:3009:35

    4S6-02 09:3510:00

    4S6-03 10:0010:15

    4S6-04 10:1510:30

    104012304S6-05 10:4010:55

    4S6-06 10:5511:10

    4S6-07 11:1011:25

    4S6-08 CREST11:3511:50

    4S6-09 11:5012:05

    4S6-10 12:0512:30

    330

    133013354S6-11 13:3013:35

    133514004S6-12 13:3514:00

    140014254S6-13 14:0014:25

    142514504S6-14 14:2514:50

    145015154S6-15 JST14:5015:15

    151515404S6-16 15:1515:40

    154016054S6-17 EL15:4016:05

    160516304S6-18 OLED OPERA 16:0516:30

    S7

    JST

    327

    930 12101S7-01 Opnening RemarksTokyo Metoro. Univ.INOUE, Haruo09:3009:40

    1S7-02 Activating solar energy fuctions in perovskite-type metal oxidesCALTECHYAMAZAKI, Yoshihiro09:4010:10

    1S7-03 In situ characterization of photo energy conversion processes at solid/liquid interfacesNIMSNOGUCHI, Hidenori10:1010:40

    1S7-04 Metal Binding by Organic Dyes under Chemical and PhotochemicalControlInst. Mol .Sci.MURAHASHI, Tetsuro10:4011:10

    1S7-05 Development of Light-energy and Molecular Material ConversionCatalysts Constructed inside a Cage-type MoleculeOsaka Univ.FUNAHASHI, Yasuhiro11:1011:40

    1S7-06 Creation of highly ecient water-splitting photocatalysts through thecontrol of surface band structureTokyo Inst.Tech.MAEDA, Kazuhiko11:4012:10

    32713201800

    1S7-07 Articial Photosynthesis Water Oxidation Is The KeyRoyal Institute of Tech. (KTH, SwedenSUN, Licheng13:2014:10

    1S7-08 Development of highly ecient water oxidation catalysts usingpolyoxometalatesHiroshima Univ.SADAKAE, Masahiro14:1014:40

    1S7-09 Optical Trapping and Photochemical Reactions/Energy Conversion ata Plasmonic Nano-AntennaOsaka City Univ.TSUBOI, Yasuyuki14:4015:10

    1S7-10 Elucidation of regulatory mechanisms of photochemical reaction inphotosynthesis to create stable molecular devicesKyoto Univ.IFUKU,Kentaro15:2515:55

    1S7-11 Elucidation of molecular mechanisms of highly ecient energyconversion and water oxidation by photosynthesis Ehime Univ.SUGIURA, Miwa15:5516:25

    1S7-12 Articial metabolic processes powered by photosynthesisKanagawaUniv.NAGASHIMA, kenji V.P.16:2516:55

    1S7-13 Multimodal spectral microscope for understanding chloroplast activityand overall cellular physiology in oil-producing algaeKyoto Univ.KUMAZAKI, Shigeichi16:5517:25

    1S7-14 Super-resolution uorescence microscopy of biomineralization indiatomsYamagata Univ.HOTTA, Jun-ichi17:2517:55

    1S7-15 Closing RemarksJST17:5518:00

    328

    133013402S7-01 13:3013:40

    134015252S7-02 13:4014:15

    2S7-03 14:1514:50

    2S7-04 14:5015:25

    153517202S7-05 15:3516:10

    2S7-06 16:1016:45

    2S7-07 --16:4517:20

  • 4

    S8 3

    327

    930 940 1S8-01 09:3009:40

    940 10101S8-02 JST-ERATO 09:4010:10

    101010401S8-03 10:1010:40

    104011001S8-04 10:4011:00

    111011301S8-05 palauamine11:1011:30

    113012001S8-06 11:3012:00

    120012301S8-07 ET743 12:0012:30

    327

    133014101S8-08 NIH 13:3013:35

    1S8-09 13:3514:10

    141014451S8-10 --14:1014:45

    144515201S8-11 PET14:4515:20

    152015551S8-12 15:2015:55

    155516301S8-13 15:5516:25

    1S8-14 16:2516:30

    328

    100010502S8-01 Visible light photoredox catalysis as key stepfor organic synthesisUniv. RegensburgOLIVER, Reiser10:0010:50

    110011502S8-02 Photosynthetic membrane architecture investi-gated by mass spectrometric analysisWashington University in St. LouisBLANKENSHIP, Robert E.11:0011:50

    328

    133014452S8-03 5 CS3 13:3013:45

    2S8-04 FLEC13:4514:15

    2S8-05 !14:1514:45

    144515452S8-06 (Mg,Li)14:4515:15

    2S8-07 15:1515:45

    154517152S8-08 CEMS15:4516:15

    2S8-09 16:1516:45

    2S8-10 16:4517:15

    21

    329

    13301700

    330

    930 10354S8-01 09:3009:35

    4S8-02 09:3509:55

    4S8-03 -09:5510:15

    4S8-04 WPI-ITbMJST-ERATO10:1510:35

    103511254S8-05 G10:3510:50

    4S8-06 WPI-ITbM10:5011:10

    4S8-07 11:1011:25

    112512154S8-08 11:2511:40

    4S8-09 11:4011:55

    4S8-10 11:5512:10

    4S8-11 12:1012:15

    330

    133015104S8-12 13:3013:35

    4S8-13 MANA 13:3514:10

    4S8-14 14:1014:40

    4S8-15 14:4015:10

  • 5

    152016304S8-16 15:2015:50

    4S8-17 JST CREST15:5016:25

    4S8-18 16:2516:30

    S9 1

    327

    930 11151S9-01 09:3009:35

    1S9-02 09:3510:00

    1S9-03 10:0010:25

    1S9-04 10:2510:50

    1S9-05 10:5011:15

    111512301S9-06 11:1511:40

    1S9-07 JST11:4012:05

    1S9-08 12:0512:25

    1S9-09 JST12:2512:30

    327

    133014251S9-10 13:3013:35

    1S9-11 13:3514:00

    1S9-12 JST 14:0014:25

    142515251S9-13 14:2514:55

    1S9-14 14:5515:25

    152516301S9-15 15:2515:55

    1S9-16 LEDJST/ERATO 15:5516:25

    1S9-17 JST 16:2516:30

    328

    133015202S9-01 13:3013:40

    2S9-02 13:4014:05

    2S9-03 JST CREST14:0514:30

    2S9-04 14:3014:55

    2S9-05 14:5515:20

    152016452S9-06 15:2015:45

    2S9-07 -JST-CREST15:4516:10

    2S9-08 JST CREST16:1016:35

    2S9-09 16:3516:45

    329

    13001700

    X

    330

    930 12304S9-01 09:3009:35

    4S9-02 X09:3510:05

    4S9-03 X 10:0510:30

    4S9-04 GISAXS10:3010:50

    4S9-05 CREST10:5011:10

    4S9-06 X11:1011:30

    4S9-07 X 11:3011:50

    4S9-08 X11:5012:10

    4S9-09 X 12:1012:30

    330

    133014304S9-10 13:3013:50

    4S9-11 13:5014:10

    4S9-12 14:1014:30

    143015304S9-13 14:3014:50

    4S9-14 14:5015:10

    4S9-15 15:1015:30

    153016304S9-16 15:3015:50

    4S9-17 15:5016:10

    4S9-18 Ge=Ge[2]16:1016:30

  • 6

    SA 2

    327

    930 12301SA-01 09:3009:50

    1SA-02 - 09:5010:20

    1SA-03 10:2010:50

    1SA-04 11:0011:30

    1SA-05 11:3012:00

    1SA-06 SiWPI-MANAJST12:0012:30

    327

    133014351SA-07 13:3013:35

    1SA-08 13:3514:05

    1SA-09 PET14:0514:35

    143515351SA-10 14:3515:05

    1SA-11 15:0515:35

    153516051SA-12 iPS15:3516:05

    160516351SA-13 16:0516:35

    Reaxys Prize Club in Japan 2014

    328

    14001700

    14 2

    329

    13151730

    330

    930 11104SA-01 1 2 309:3009:55

    4SA-02

    09:5510:204SA-03 10:2010:45

    4SA-04 10:4511:10

    111012304SA-05 Si""NTT 11:1011:35

    4SA-06 11:3512:00

    4SA-07 12:0012:25

    4SA-08 12 : 2512:30

    330

    133014504SA-09 13:3013:50

    4SA-10 13:5014:10

    4SA-11 JST 14:1014:30

    4SA-12 14:3014:50

    151016304SA-13 Kim 15:1015:30

    4SA-14 15:3015:50

    4SA-15 1 15:5016:10

    4SA-16 16:1016:30

    SB S21

    329

    13301740

  • 7

    (ATP)

    F4 S10

    327

    130013101F4-25 13:0013:10

    131016501F4-26 13:1013:40

    1F4-29 Unstructured/Structured Interaction13:4014:10

    1F4-32 HGF14:1014:40

    1F4-35 14:4015:001F4-37 15:0015:30

    1F4-40 15:3016:00

    1F4-43 Phoenix Venture Partners (PVP)16:0016:30

    1F4-46 16:3016:50

    328

    920 11002F4-03 09:2009:30

    2F4-04 (FCEV)09:3010:20

    2F4-09 45 PEFC10:2010:50

    2F4-12 10:5011:00

    110012102F4-13 11:0011:40

    2F4-17 PEFC 11:4012:10

    328 13101520

    2F4-26 13:1014:00

    2F4-31 14:0014:40

    2F4-35 I2CNER14:4015:10

    2F4-38 15:1015:20

    152017202F4-39 Bloom EnergyJapan15:2016:00

    2F4-43 16:0016:40

    2F4-47 16:4017:20

    329

    130013103F4-25 13:0013:10

    131014503F4-26 13:1014:00

    3F4-31 14:0014:40

    3F4-35 14:4014:50

    145016103F4-36 14:5015:30

    3F4-40 JST-CREST15:3016:10

    161017003F4-44 16:1016:40

    3F4-47 16:4017:00

    F5 S11

    327

    900 10401F5-01 WPI-AIMR09:0009:101F5-02 LIXIL09:1009:40

    1F5-05 09:4010:10

    1F5-08 VOIGT Dagmar10:1010:40

    104012201F5-11 10:4011:10

    1F5-14 11:1011:40

    1F5-17 11:4012:20

    327 12501410

    1F5-24 12:5013:40

    1F5-29 TRIZ 13:4014:10

    141015401F5-32 14:1014:40

    1F5-35 RGB14:4015:10

  • 8

    1F5-38 15:1015:40

    154017201F5-41 15:4016:10

    1F5-44 R&D 16:1016:40

    1F5-47 16:4017:20

    328

    101010202F5-08 10:1010:20

    102012002F5-09 10:2011:10

    2F5-14 11:1011:202F5-15 GSC11:2012:00

    328 13001410

    2F5-25 13:0013:30

    2F5-28 13:3014:00

    2F5-31 14:0014:10

    141015302F5-32 14:1014:50

    2F5-36 14:5015:20

    2F5-39 15:2015:30

    153016002F5-40 ( )15:3016:00

    160016102F5-43 16:0016:10

    329

    130013103F5-25 13:0013:10

    131014203F5-26 PE PET 13:1013:50

    3F5-30 GP13:5014:20

    142015403F5-33 14:2014:50

    3F5-36 14:5015:003F5-37 QMONOS15:0015:40

    154017003F5-41 15:4016:10

    3F5-44 PET16:1016:50

    3F5-48 16:5017:00

    G6 S20

    327

    133015301G6-28 13:3013:401G6-29 13:4014:30

    1G6-34 14:3014:401G6-35 14:4015:20

    1G6-39 15:2015:30

    153017101G6-40 CNT 15:3016:10

    1G6-44 16:1016:201G6-45 16:2017:00

    1G6-49 17:0017:10

    328

    930 940 2G6-04 JX09:3009:40

    940 12002G6-05 09:4010:30

    2G6-10 10:3010:402G6-11 10:4011:20

    2G6-15 11:2012:00

    328 13001550

    2G6-25 5-13:0013:40

    2G6-29 13:4014:20

    2G6-33 14:2014:302G6-34 ACT-C 14:3015:10

    2G6-38 15:1015:50

    329

    920 12103G6-03 09:2009:303G6-04 09:3010:20

    3G6-09 10:2010:30

  • 9

    3G6-10 JST/ACT-C10:3011:10

    3G6-14 11:1011:203G6-15 11:2012:00

    3G6-19 12:0012:10

    329 13101450

    3G6-26 I2CNER : Powering the Future, InternationalizingResearchI2CNER, Kyushu Univ.SOFRONIS, Petros13:1014:00

    3G6-31 Incubation Time14:0014:103G6-32 14:1014:40

    3G6-35 14:4014:50

    150016403G6-37 15:0015:40

    3G6-41 15:4015:503G6-42 Lignocellulose 15:5016:30

    3G6-46 16:3016:40

    G7 S21

    327

    122015001G7-21 12:2013:10

    1G7-26 13:1013:40

    1G7-29 - -13:4014:20

    1G7-33 14:2014:50

    1G7-36 14:5015:00

    150017201G7-37 15:0015:40

    1G7-41

    15:4016:201G7-45 16:2016:50

    1G7-48 16:5017:20

    H5 S30

    327

    100010101H5-07 FLEC10:0010:10

    101012101H5-08 10:1011:00

    1H5-13 Li11:0011:40

    1H5-17 11:4012:10

    327 13101450

    1H5-26 13:1013:50

    1H5-30 FLEC 13:5014:20

    1H5-33 JST/ERATO14:2014:50

    151016501H5-38 Development of Taste Sensing SystemFac. Sci. Tech.,Keio Univ.CITTERIO, Daniel; SUZUKI, Koji15:1015:50

    1H5-42 JSRJSR 15:5016:20

    1H5-45 NVRAM16:2016:50

    328 900 1200

    2H5-01 09:0009:40

    2H5-05 09:4010:10

    2H5-09 10:2011:00

  • 10

    2H5-13 TFT 11:0011:30

    2H5-16 EL11:3012:00

    328

    130013102H5-25 13:0013:10

    131015102H5-26 13:1014:00

    2H5-31 14:0014:30

    2H5-34 iCeMS 14:3015:10

    153017102H5-40 15:3016:10

    2H5-44 16:1016:40

    2H5-47 16:4017:10

    329 920 1040

    3H5-03 09:2010:00

    3H5-07 10:0010:40

    104012203H5-11 XJST10:4011:10

    3H5-14 11:1011:50

    3H5-18 11:5012:20

    329 13301530

    3H5-28 13:3014:20

    3H5-33 14:2014:50

    3H5-36 14:5015:30

    155017303H5-42 15:5016:20

    3H5-45 JST 16:2017:00

    3H5-49 17:0017:30

    330 10001230

    4H5-07 CZTS 10:0010:40

    4H5-11 CZTS 10:4011:10

    4H5-14 11:1011:50

    4H5-18 11:5012:30

    P

    32712301400

    1PB-201

    1PB-202

    1PB-203 NEC

    1PB-204 X ICP-MS CO2

    1PB-205 CO2

    1PB-206 (SqRAFTwP)

    1PB-207 CO2

    1PB-208

    1PB-209

    1PB-210

    1PB-211

    1PB-212 GaN LED

    1PB-213

    1PB-214

    1PB-215

    1PB-216

    1PB-217 Cu Cu

    1PB-218 D-A

    1PB-219

    1PB-220

    1PB-221

    1PB-222

  • 11

    1PB-223 FLEC

    1PB-224 BNCT BNCT

    1PB-225 BNCT

    1PB-226 -1,3-

    1PB-227 JVCJVC

    1PB-228

    1PB-229 in vivo

    1PB-230 Rational design of spirocyclic rhodamine derivatives for multi-colorcancer imagingGrad. Sch. Med., The Univ. of Tokyo; Grad. Sch. Pharm.,The Univ. of Tokyo; JST Basic Research ProgramIWATATE, Ryu john;KAMIYA, Mako; URANO, Yasuteru

    1PB-231

    1PB-232 1-acetoxychavicol acetate (ACA)

    1PB-233

    1PB-234

    1PB-235 IER5/Cdc25B

    1PB-236 HasA

    1PB-237

    1PB-238 Design and synthesis of antimalarial agents with indoloquinolonecoresGrad. Sch. Nat. Sci. Technol., Okayama Univ.WANG, Ning; LU,Wen-jie; HAYASHI, Ikuya; KAWAFUCHI, Hiroyuki; INOKUCHI,

    Tsutomu

    1PB-239 Network structures in polysaccharide gels and its eect onswallowingGrad. Sch. Marine Sci. and Technol., Tokyo Univ. of MarineSci. and Technol.MATSUKAWA, Shingo; BRENNER, Tom; SHIMADA,Ryota

    1PB-240

    1PB-241

    1PB-242

    1PB-243 TIMP

    32715001630

    1PC-201 JST ,C R E S T MUCKERMAN James T.

    1PC-202 SPS

    1PC-203

    1PC-204 CaMn2O4*xH2O

    1PC-205

    1PC-206

    1PC-207

    1PC-208 GaN-Si

    1PC-209 CO2

    1PC-210 Block Copolymer-Mediated Transfer Printing of Nanostructures:Application in Solar CellsAIST Renewable Energy Research CenterMIZUNO, Hidenori; SAI, Hitoshi; MATSUBARA, Koji; KONDO, Michio

    1PC-211

    1PC-212

    1PC-213 JST

    1PC-214

    1PC-215 JST CREST

    1PC-216

    1PC-217 JST CREST

    1PC-218 Cs

    1PC-219

    1PC-220

    1PC-221

    1PC-222 5cm

    1PC-223 WANGWanhuiMUCKERMAN James T.

    1PC-224 Y/N

    1PC-225

    1PC-226

    1PC-227

    1PC-228

    GSC1PC-229

    1PC-230

    1PC-231

    1PC-232

    1PC-233

  • 12

    1PC-234 N-

    1PC-235 /JST CRESTUYANIK Muhammet

    1PC-236

    1PC-237 --

    1PC-238

    1PC-239 Boronic Acid-DMAP(O) Cooperative Catalysis for DehydrativeCondensation between Carboxylic Acids and AminesGrad. Sch. Eng.,Nagoya Univ.LU, Yanhui; ISHIHARA, Kazuaki

    1PC-240 -

    1PC-241

    1PC-242 Optical properties of confeito-like Au nanoparticles and theirapplicationsNational Univerisity of Science and TechnologyUJIHARA,Masaki; IMAE, Toyoko

    1PC-243

    1PC-244

    1PC-245 PEG

    1PC-246

    1PC-247

    1PC-248

    1PC-249

    1PC-250 P450BM3

    1PC-251

    1PC-252

    1PC-253

    1PC-254

    1PC-255

    1PC-256

    1PC-257

  • 13

    (AP)

    A1 7

    F

    327

    950 1050 PC 9409501A1-06, 1A1-07, 1A1-08, 1A1-09,

    1A1-10, 1A1-111A1-06 :WPI-ITbM

    1A1-07 (1--2-)

    1A1-08

    1A1-09 C2

    1A1-10 1-

    1A1-11 (S)-trans-

    11001200 PC 105011001A1-13, 1A1-14, 1A1-15, 1A1-16,

    1A1-171A1-13 5,10-[5]

    1A1-14 [33](1,3,5) Si-Si Aung

    1A1-15 [2+2]

    1A1-16 1,2-, 1,3- 2-

    1A1-17* Synthesis and Photochemical Reactivity of Caged-compounds withNovel Stilbene-based Two-photon ChromophoreGrad. Sch. Sci., HiroshimaUniv.BOINAPALLY, Srikanth; ABE, Manabu

    327 13101410

    PC 130013101A1-26, 1A1-29, 1A1-301A1-26

    1A1-29 2-

    1A1-30*

    14201520 PC 141014201A1-33, 1A1-34, 1A1-35, 1A1-36,

    1A1-381A1-33 2,5--3,6--1,4-()

    1A1-34

    1A1-35

    1A1-36* CC

    1A1-38 2,6-

    15301630 PC 152015301A1-40, 1A1-41, 1A1-42, 1A1-43,

    1A1-44, 1A1-45

    1A1-40 (9-)()

    1A1-41 DNA ATS

    1A1-42 DNA

    1A1-43

    1A1-44 -5 PEG-

    1A1-45

    16401730 PC 163016401A1-47, 1A1-48, 1A1-49, 1A1-50,

    1A1-511A1-47

    1A1-48

    1A1-49

    1A1-50

    1A1-51 REMELLO SebastianNybin

    328 950 1050

    PC 9409502A1-06, 2A1-07, 2A1-08, 2A1-09,2A1-10

    2A1-06

    2A1-07

    2A1-08 Kuttassery FazalurahmanMathew Siby

    2A1-09 ALCA, JST

    2A1-10* Re CO2XAFS

    11001200 PC 105011002A1-13, 2A1-14, 2A1-15, 2A1-16,

    2A1-17, 2A1-182A1-13

    2A1-14

    2A1-15 (III)

    2A1-16

    2A1-17 Viviani Vadim

    2A1-18

    328 13101410

    PC 130013102A1-26, 2A1-27, 2A1-28, 2A1-29,

  • 14

    2A1-30, 2A1-312A1-26 1

    2A1-27 2

    2A1-28 -

    2A1-29

    2A1-30

    2A1-31

    A2 8

    B

    327

    920 1010 PC 9109201A2-03, 1A2-04, 1A2-05, 1A2-06,

    1A2-071A2-03

    1A2-04

    1A2-05 --

    1A2-06

    1A2-07

    10201100 PC 101010201A2-09, 1A2-10, 1A2-11, 1A2-121A2-09 [2+2]

    1A2-10 Regioselective synthesis of 1,4-bisfunctionalized fullerenes via NBS-promoted oxidation of fullerene monoradicalWPI-AIMR, Tohoku Univ.SI, Weili; ASAO, Naoki; YAMAMOTO, Yoshinori; JIN, Tienan

    1A2-11 [5] INCS

    1A2-12 INCS

    11101150 PC 110011101A2-14, 1A2-15, 1A2-16, 1A2-171A2-14

    1A2-15

    1A2-16 [2+2+2]S

    1A2-17 Iterative Suzuki-Miyaura Coupling for Oligo(naphthalene-2,3-diyl)swith a Chiral Terminal Boronyl Group: Synthesis and Control of the Chiral

    ConformationGrad. Sch. Eng., Kyoto Univ.ISHIBASHI, Aoi;YAMAMOTO, Takeshi; SUGINOME, Michinori

    327 13001400

    PC 125013001A2-251A2-25

    14101500 PC 140014101A2-32, 1A2-33, 1A2-34, 1A2-351A2-32 Suzuki

    1A2-33 Diels-Alder

    1A2-34 E

    1A2-35* 132

    15101600 PC 150015101A2-38, 1A2-40, 1A2-41, 1A2-421A2-38*

    1A2-40 C2v

    1A2-41

    1A2-42 The synthesis of ethynylhelicene oligomers with gunidinium terminusGrad. Sch. Pharm. Sci., Tohoku Univ.SAITO, Nozomi; YAN, Liwei;YAMAGUCHI, Masahiko

    16101650 PC 160016101A2-44, 1A2-45, 1A2-46, 1A2-471A2-44 N-(III

    1A2-45

    1A2-46 4,4--o-

    1A2-47 1,2-(5-)

    17001750 PC 165017001A2-49, 1A2-50, 1A2-51, 1A2-52,

    1A2-531A2-49

    1A2-50

    1A2-51

    1A2-52 p J STCREST

    1A2-53

    328 900 950

    PC 8509002A2-01, 2A2-02, 2A2-03, 2A2-04,2A2-05

    2A2-01

    2A2-02

    2A2-03

    2A2-04

    2A2-05 Grignard(

    10001050 PC 95010002A2-07, 2A2-08, 2A2-09, 2A2-102A2-07

    2A2-08

    2A2-09 C-Ho-

    2A2-10*

  • 15

    11001150 PC 105011002A2-13, 2A2-15, 2A2-16, 2A2-172A2-13*

    2A2-15

    2A2-16 3

    2A2-17 -Pictet-Spengler

    328 13001350

    PC 125013002A2-25, 2A2-26, 2A2-27, 2A2-282A2-25 1 Grignard

    2A2-26 1

    2A2-27 1

    2A2-28* Oxidative Dimerization of (Hetero)aromatic Amines Utilizing tert-Butyl Hypoiodite Leading to (Hetero)aromatic Azo CompoundsGrad. Sch.Eng., Osaka Univ.OKUMURA, Sota; LIN, Chun-hsuan; TAKEDA,Youhei; MINAKATA, Satoshi

    14001450 PC 135014002A2-31, 2A2-33, 2A2-34, 2A2-352A2-31* Ecient synthesis of multisubstituted benzofurans from phenols byextended Pummerer reactionGrad. Sch. Sci., Kyoto Univ.MURAKAMI,Kei; YORIMITSU, Hideki; OSUKA, Atsuhiro

    2A2-33 defucogilvocarcin M

    2A2-34

    2A2-35 3,3,5,5-

    15001550 PC 145015002A2-37, 2A2-38, 2A2-39, 2A2-40,

    2A2-412A2-37 N-

    2A2-38 BiAr3

    2A2-39

    2A2-40

    2A2-41

    16001650 PC 155016002A2-43, 2A2-44, 2A2-45, 2A2-46,

    2A2-472A2-43

    2A2-44

    2A2-45 2

    2A2-46

    2A2-47 Birch

    329 900 950

    PC 8509003A2-01, 3A2-02, 3A2-03, 3A2-04,3A2-05

    3A2-01 Selective hydrogenation of nitroarenes catalyzed by Pd-based alloy

    nanoparticlesWPI-AIMR, Tohoku Univ.; Grad. Sch. Sci., Tohoku Univ.YANG, Lin; ZHAO, Ming; ASAO, Naoki

    3A2-02

    3A2-03

    3A2-04 RC

    3A2-05

    10001040 PC 95010003A2-07, 3A2-08, 3A2-093A2-07

    3A2-08

    3A2-09*

    10501130 PC 104010503A2-12, 3A2-14, 3A2-153A2-12* RCIS

    3A2-14 RCIS

    3A2-15 2-

    A3 5

    C

    327

    900 1000 PC 8509001A3-01, 1A3-02, 1A3-04, 1A3-05,

    1A3-061A3-01

    1A3-02*

    1A3-04 [4+1]

    1A3-05 [3+2]

    1A3-06

    10101110 PC 100010101A3-08, 1A3-09, 1A3-10, 1A3-12,

    1A3-131A3-08 L- Stemaphylline

    1A3-09

    1A3-10*

    1A3-12 1,2,3-

    1A3-13 ---

    11201220 PC 111011201A3-15, 1A3-16, 1A3-18, 1A3-19,

    1A3-201A3-15 1,6-

  • 16

    1A3-16* Reformatsky

    1A3-18 -Michael

    1A3-19 C-H

    1A3-20

    327 13301430

    PC 132013301A3-28, 1A3-29, 1A3-30, 1A3-31,1A3-32, 1A3-33

    1A3-28 2,3-[3+2]Arteaga Fernando ArteagaNGUYEN Tue Minh-Nhat

    1A3-29

    1A3-30

    1A3-31 2- C2

    1A3-32

    1A3-33 N-

    14401540 PC 143014401A3-35, 1A3-36, 1A3-37, 1A3-38,

    1A3-39, 1A3-401A3-35

    1A3-36 2-

    1A3-37

    1A3-38

    1A3-39

    1A3-40 1,3--5-

    15501650 PC 154015501A3-42, 1A3-43, 1A3-44, 1A3-45,

    1A3-46, 1A3-471A3-42

    1A3-43

    1A3-44 PN

    1A3-45 E/Z

    1A3-46 1,4--1,2,3--5-

    1A3-47 2--2- 6

    17001740 PC 165017001A3-49, 1A3-50, 1A3-51, 1A3-521A3-49 8, 8-

    1A3-50

    1A3-51 Mn()

    1A3-52 Mn(III)

    17501830 PC 174017501A3-54, 1A3-55, 1A3-56, 1A3-57

    1A3-54 ,-

    1A3-55 1,3--1,3- 1,3-

    1A3-56 N-

    1A3-57

    328 900 1000

    PC 8509002A3-01, 2A3-02, 2A3-03, 2A3-04,2A3-06

    2A3-01

    2A3-02 N- 8 C-H

    2A3-03

    2A3-04* Asymmetric synthesis and catalytic activities of novel avinium saltsThe University of Toledo Department of ChemistryYAMAMOTO, Kana;ARIMITSU, Kenji; ALMALITI, Jehad

    2A3-06

    10101110 PC 100010102A3-08, 2A3-10, 2A3-11, 2A3-12,

    2A3-132A3-08* SHi

    2A3-10 Diels-Alder

    2A3-11 8

    2A3-12 Furoxan

    2A3-13 - 2,3-

    11201220 PC 111011202A3-15, 2A3-16, 2A3-17, 2A3-18,

    2A3-19, 2A3-202A3-15

    2A3-16

    2A3-17 Diels-Alder

    2A3-18 2--3,1--4- 2--3,1--4-

    2A3-19

    2A3-20 1,5-

    328 13301430

    PC 132013302A3-28, 2A3-29, 2A3-30, 2A3-31,2A3-32, 2A3-33

    2A3-28 2

    2A3-29 2,2--1,1- N-[c]

    2A3-30

    2A3-31

    2A3-32 O- 2,3--[4+2]

  • 17

    2A3-33 1,3-

    329 900 950

    PC 8509003A3-01, 3A3-02, 3A3-03, 3A3-053A3-01 3

    3A3-02 5-

    3A3-03* Synthesis of 2-Aryl-5-nitropyridines by Three Component RingTransformation of 3,5-Dinitro-2-pyridoneKUTLE, Thi song;ASAHARA, Haruyasu; SUGIMOTO, Ryuichi; KOBIRO, Kazuya; SAIGO,

    Kazuhiko; NISHIWAKI, Nagatoshi

    3A3-05 N-

    10001050 PC 95010003A3-07, 3A3-09, 3A3-10, 3A3-113A3-07* Regioselective Rapid Synthesis of Fully Substituted 1,2,3-TriazolesMediated by Propargyl CationsGrad. Sch. Mat. Sci., NAISTZHANG,Huan; TANIMOTO, Hiroki; KAKIUCHI, Kiyomi

    3A3-09 N-

    3A3-10 1,3,5-[1,5-a]

    3A3-11 [1,5-a]

    11001150 PC 105011003A3-13, 3A3-15, 3A3-16, 3A3-173A3-13* tert- C4h

    3A3-15 1,3,4-

    3A3-16

    3A3-17

    A

    329

    13101410 PC 130013103A3-26, 3A3-28, 3A3-30, 3A3-313A3-26* Synthesis and Characterization of Rotaxanes Possessing ThermallyDegradable CounteranionsGrad. Sch. Sci., Eng., Tokyo TechZHU, Nan;ABE, Yoko; NAKAZONO, Kazuko; TAKATA, Toshikazu

    3A3-28*

    3A3-30 NMRPhan Son Thanh

    3A3-31

    14201510 PC 141014203A3-33, 3A3-35, 3A3-36, 3A3-373A3-33* Novel cyclic amide oligomer containing pi-conjugated unit: Designand chiral characterizationNagoya Inst. of Tech. Grad. School of Eng.YAMAKADO, Ryohei; MATSUOKA, Sin-ichi; SUZUKI, Masato;

    TAKAGI, Koji; MASU, Hyuma; TAKEUCHI, Daisuke; AZUMAYA, Isao

    3A3-35 2-

    3A3-36 9,10-

    3A3-37

    15201620 PC 151015203A3-39, 3A3-41, 3A3-42, 3A3-43,

    3A3-443A3-39*

    3A3-41 S X

    3A3-42

    3A3-43

    3A3-44 JST CREST

    330 900 1000

    PC 8509004A3-01, 4A3-02, 4A3-03, 4A3-04,4A3-05, 4A3-06

    4A3-01

    4A3-02 MAURIZOTVictor HUC Ivan

    4A3-03 4,8-

    4A3-04

    4A3-05

    4A3-06 [6]Cycloparaphenylene

    10101110 PC 100010104A3-08, 4A3-10, 4A3-11, 4A3-12,

    4A3-134A3-08* Conformational Analysis of Single Peruoroalkyl Chains by Single-Molecule Real-Time Transmission Electron Microscopic ImagingGrad. Sch.Sci., The Univ. of Tokyo; NTRC, AISTHARANO, Koji; TAKENAGA,Shinya; OKADA, Satoshi; NIIMI, Yoshiko; YOSHIKAI, Naohiko; ISOBE,

    Hiroyuki; SUENAGA, Kazu; KATAURA, Hiromichi; KOSHINO, Masanori;

    NAKAMURA, Eiichi

    4A3-10 CH/

    4A3-11 X

    4A3-12 JST CREST

    4A3-13 XJST

    11201200 PC 111011204A3-15, 4A3-16, 4A3-17, 4A3-184A3-15 MiranMohammed

    4A3-16 UV-vis

    4A3-17 DPPH Cl

    4A3-18

    A4 1

    A

    327

    10101110 PC 100010101A4-08, 1A4-09, 1A4-10, 1A4-11,

    1A4-121A4-08

    1A4-09 25

  • 18

    1A4-10

    1A4-11 ()

    1A4-12* (AIE) (PeT)

    11201220 PC 111011201A4-15, 1A4-17, 1A4-18, 1A4-19,

    1A4-201A4-15* Environment-Responsive Fluorescent Probe Containing a PhospholeOxideGrad. Sch. Sci., Nagoya Univ.YAMAGUCHI, Eriko;FUKAZAWA, Aiko; KOSAKA, Youhei; SATO, Yoshikatsu; SASAKI,

    Taeko; UEDA, Minako; SASAKI, Narie; HIGASHIYAMA, Tetsuya;

    YAMAGUCHI, Shigehiro

    1A4-17 2,5- ESIPTWPI-ITbM

    1A4-18

    1A4-19 1,8-(-1-)

    1A4-20 1-Acetylaminopyrene

    327 13301430

    PC 132013301A4-28, 1A4-29, 1A4-30, 1A4-31,1A4-32, 1A4-33, 2A4-28, 2A4-29, 2A4-30, 2A4-31, 2A4-32

    1A4-28

    1A4-29 (CPL)

    1A4-30 (CPL)

    1A4-31 (CPL)

    1A4-32

    1A4-33

    B

    328

    133014202A4-28 -1,3-

    2A4-29

    2A4-30 ALCA,JST

    2A4-31 2--3--(E)--1-

    2A4-32 5-exo6-endo

    14301530 PC 142014302A4-34, 2A4-36, 2A4-37, 2A4-382A4-34* Si-Si[2 + 1]

    2A4-36 [2+2]

    2A4-37 4,4-1,2--3,5-

    2A4-38*

    15401630 PC 153015402A4-41, 2A4-42, 2A4-43, 2A4-44,

    2A4-452A4-41 -

    2A4-42 : 31P NMR

    2A4-43

    2A4-44 C-C-

    2A4-45

    16401730 PC 163016402A4-47, 2A4-49, 2A4-502A4-47* Decoration of Porous Coordination Polymers with Nitroxyl Radicalsfor Selectively Catalytic Oxidation of AlcoholsiCeMS, Kyoto Univ.LI,Liangchun; MATSUDA, Ryotaro; KITAGAWA, Susumu

    2A4-49

    2A4-50*

    Asian International Symposium-Photochemistry-

    329

    100010103A4-07 Opening addressOsaka UniversityMajima, Tetsuro10:0010:10

    Chair: Ohta, Nobuhiro101010503A4-08 Keynote Lecture Studies of unimolecular photodissociationdynamics using synchrotron VUV ionizationNSRRCLee, Shih-Huang10:1010:50

    Chair: Tamai, Naoto111011503A4-14 Invited Lecture Functionalization of titanium oxide by metalcomplex modication and its application to energy and molecular transforma-

    tionsKyushu UniversityShimakoshi, Hisashi11:1011:303A4-16 Invited Lecture Photoswitching of biological functions based onthe photoisomerization of azobenzenesHokkaido UniversityFukaminato,Tsuyoshi11:3011:50

    329Chair: Karatsu, Takashi13001340

    3A4-25 Keynote Lecture Optical gain in strongly quantum connedcolloidal semiconductor nanostructuresNational University of SingaporeChan, Yin Thai13:0013:40

    Chair: Arai, Tatsuo140014403A4-31 Invited Lecture Developing Metal-Polycyclic-Aromatic-Hydro-carbons Into a New Class of Organometallic Emitters and Photosensitizers

    National University of SingaporeYip, John H. K.14:0014:40

    Chair: Majima, Tetsuro150016003A4-37 Keynote Lecture Eco-driven environmetal remediation and H2generation based on photocatalytic and photoelectrocatalytic techniques

    Shanghai Normal UniversityLi, Guisheng15:0015:403A4-41 Invited Lecture Design and application of TiO2-based photo-functional materialsOsaka UniversityKamegawa, Takashi15:4016:00

    Chair: Yasuda, Masahide162017303A4-45 Invited Lecture DNA scaolded chromophore aggregates andtheir photochemical behaviorUniversity of HyogoNakamura, Mitsunobu16:2016:40

    3A4-47 Invited Lecture Photosensitized damage of DNA and proteinShizuoka UniversityHirakawa, Kazutaka16:4017:00

    3A4-49 Invited Lecture Thermoswitchable Emission and Colora-tion of a Composite Material Containing a Luminescent Lantha-

    nide(III) Complex and Fluoran DyeChiba UniversityNakamura, Kazuki17:0017:20

    3A4-51 Closing addressNational University of SingaporeYip, John H. K.17:2017:30

  • 19

    A

    330

    900 1000 PC 8509004A4-01, 4A4-02, 4A4-03, 4A4-04,

    4A4-05, 4A4-064A4-01

    4A4-02

    4A4-03 Push-pull 1,5-

    4A4-04 1,8-

    4A4-05 / OPERA

    4A4-06

    10101110 PC 100010104A4-08, 4A4-10, 4A4-11, 4A4-12,

    4A4-134A4-08* Didier PascalMely YvesKlymchenko Andrey

    4A4-10

    4A4-11

    4A4-12 2-()

    4A4-13 [2.2]

    11201220 PC 111011204A4-15, 4A4-17, 4A4-18, 4A4-19,

    4A4-204A4-15* Nonlinear Optical Eects related to Aromatic Polyimide Conforma-tionGrad. Sch. Sci., Eng., Tokyo TechSHIRATA, Kei; HATTORI,Masaya; MIYAWAKI, Ryousuke; KAWAUCHI, Susumu

    4A4-17 (4) CMSJST-CREST

    4A4-18 (5) CMSJST-CREST

    4A4-19 N,N-/OPERA

    4A4-20 EL

    330

    13301410 PC 132013304A4-28, 4A4-29, 4A4-304A4-28

    4A4-29 J

    4A4-30* Synthesis of diyne-labeled sphingomyelin and evaluation of its raft-likedomain formationSch. Sci., Osaka Univ.CUI, Jin; KINOSHITA,Masanao; MATSUOKA, Shigeru; SATO, Fuminori; ANDO, Jun;

    YAMAGOSHI, Hiroyuki; DODO, Koyuke; FUJITA, Katsumasa;

    SODEOKA, Mikio; MURATA, Michio

    14201450 PC 141014204A4-33, 4A4-34, 4A4-354A4-33 -

    4A4-34

    4A4-35

    15001520 PC 145015004A4-37, 4A4-384A4-37

    4A4-38

    15301550 PC 152015304A4-40, 4A4-414A4-40

    4A4-41

    A5 2

    A

    327

    900 940 PC 8509001A5-01, 1A5-02, 1A5-031A5-01

    1A5-02

    1A5-03* Porous Molecular Networks on Graphene Formed by Self-Assemblyof Dehydrobenzo[12]annulene DerivativesGrad. Sch. Eng. Sci., Osaka Univ.;JST-PRESTO; KU Leuven-University of Leuven Department of Chemistry,TAHARA, Kazukuni; LI, Bing; ADISOEJOSO, Jinne; VANDERLINDEN,

    Willem; DE GENDT, Stefan; DE FEYTER, Steven; TOBE, Yoshito

    950 1030 PC 9409501A5-06, 1A5-081A5-06*

    1A5-08* /MANA/WPI-MANA

    10401120 PC 103010401A5-11, 1A5-13, 1A5-141A5-11* WPI-TIbMJST-JST-CREST

    1A5-13

    1A5-14

    11301200 PC 112011301A5-16, 1A5-17, 1A5-181A5-16 MOF

    1A5-17

    1A5-18 -

    12101230 PC 120012101A5-20, 1A5-211A5-20 8 -

  • 20

    1A5-21

    327 13401410

    PC 133013401A5-29, 1A5-30, 1A5-311A5-29

    1A5-30

    1A5-31

    14201440 PC 141014201A5-33, 1A5-341A5-33

    1A5-34

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    329

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  • 21

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  • 22

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  • 23

    328

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    2A6-09* A Bis(2-hydroxyphenyl)pyrimidine-bridged Multiple Molecular SpurGears: Synthesis and Dynamic Motions.Chem. Res. Lab., Tokyo TechTSUCHIDO, Yoshitaka; SUZAKI, Yuji; OSAKADA, Kohtaro

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    328 13301430

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    2A6-45* Supramolecular Corannulene FiberRIKEN CEMSMIYAJIMA,Daigo; KANG, Jiheong; AIDA, Takuzo

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    329 900 1000

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  • 24

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    3A6-543A6-49* Extraction of Pd(II) ions with dimethyl(thiocarbamoyl) modifiedthiacalix[n]arenesFac. Eng. Resource Sci., Akita Univ.MUNIYAPPAN,Rajiv gandhi; YAMADA, Manabu; KONDO, Yoshihiko; HAMADA, Fumio

    3A6-51

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    4A6-20 Pillar[5]arene

    330 13301430

    PC 132013304A6-28, 4A6-30, 4A6-31, 4A6-32,4A6-33

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    14401540 PC 143014404A6-35, 4A6-36, 4A6-38, 4A6-39,

    4A6-404A6-35 Au(I)

    4A6-36* Self-Assembly of Boroxine CagesGrad. Sch. Sci., Eng., Tokyo Tech;JST CRESTONO, Kosuke; IWASAWA, Nobuharu

    4A6-38

    4A6-39

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    15501640 PC 154015504A6-42, 4A6-43, 4A6-44, 4A6-45,

    4A6-46

  • 25

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    A7 5 12

    A

    327

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    10101100 PC 100010101A7-08, 1A7-09, 1A7-10, 1A7-121A7-08 JST

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    327 13201400

    PC 131013201A7-27, 1A7-29, 1A7-301A7-27* Five-Fold Symmetric Penta-Bioconjugated Corannulenes: Synthesis,Properties and ApplicationsTohoku Univ. Department of Chemistry andWPI-AIMRMATTARELLA, Martin; SIEGEL, Jay

    1A7-29 9,10-()

    1A7-30 Syntheses and Structual Characterization of Pyrene-Based MetalComplexesGrad. Sch. Sci. Eng., Tokyo Metropolitan Univ.LUONG,Xuan-dien; YAMASHITA, Ken-ichi; ASANO, Motoko; SUGIURA, Ken-ichi

    14101450 PC 140014101A7-32, 1A7-33, 1A7-34, 1A7-351A7-32

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    1A7-34

    1A7-35 [3.3.3]

    17101800 PC 170017101A7-50, 1A7-52, 1A7-53, 1A7-541A7-50*

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    18101900 PC 180018101A7-56, 1A7-57, 1A7-58, 1A7-591A7-56 ZHAIXue

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    328

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    2A7-19 3,7-

    2A7-20 [4n]

  • 26

    328 13301420

    PC 132013302A7-28, 2A7-29, 2A7-30, 2A7-31,2A7-32

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    2A7-31

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    14301520 PC 142014302A7-34, 2A7-37, 2A7-382A7-34 //

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    2A7-50

    329

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    329 13201420

    PC 131013203A7-27, 3A7-28, 3A7-29, 3A7-30,3A7-31, 3A7-32

    3A7-27

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    14301530 PC 142014303A7-34, 3A7-35, 3A7-37, 3A7-38,

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    3A7-35* -

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    15401640 PC 153015403A7-41, 3A7-43, 3A7-44, 3A7-45,

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    3A7-46 ABC

    16501750 PC 164016503A7-48, 3A7-49, 3A7-50, 3A7-51,

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    3A7-49 -

  • 27

    3A7-50

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    3A7-52

    3A7-53

    18001850 PC 175018003A7-55, 3A7-57, 3A7-58, 3A7-593A7-55* Two Terminal Wired Single Molecular Diodes of Porphyrin-ImideConnected to Single-Walled Carbon NanotubesOsaka Univ.MURNI,Handayani; GODA, Shun; TANAKA, Hirofumi; TANAKA, Daisuke;

    KATAYOSE, Shinichi; OGAWA, Takuji

    3A7-57 meso-

    3A7-58

    3A7-59 -

    330

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    4A7-02

    4A7-03

    10001050 PC 95010004A7-07, 4A7-08, 4A7-09, 4A7-10,

    4A7-114A7-07 8 3WPI-ITbM JST- JST-CREST YUAN ChunxueCAMACHO CristopherIRLE Stephane

    4A7-08 PCET

    4A7-09

    4A7-10 1H-[de]-4,5-()

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    11001150 PC 105011004A7-13, 4A7-14, 4A7-15, 4A7-164A7-13

    4A7-14

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    4A7-16* [n]

    330 13001350

    PC 125013004A7-25, 4A7-26, 4A7-27, 4A7-284A7-25

    4A7-26 5,11-[3,2-b]

    4A7-27 [a,j]

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    14001450 PC 135014004A7-31, 4A7-32, 4A7-33, 4A7-34,

    4A7-354A7-31 2,3-(1-)-1,3- Diels-Alder

    4A7-32

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    15001600 PC 145015004A7-37, 4A7-38, 4A7-39, 4A7-40,

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    16101650 PC 160016104A7-44, 4A7-45, 4A7-464A7-44 1

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    4A7-46* Ion Conductivity of Multi-interactive TPHAP Derivatives Based onTheir Assembled StructuresPOSTECHYAKIYAMA, Yumi; LEE, Gil-ryeong; MORITA, Yasushi; KAWANO, Masaki

    B1 ES101(ES)

    E

    327

    B

    900 1000 PC 8509001B1-01, 1B1-02, 1B1-03, 1B1-04,

    1B1-05, 1B1-061B1-01 Enantioselective Synthesis of -Chiral (E)--Alkoxyallylboronatesvia Copper(I)-Catalyzed Nucleophilic -Boryl-Substitution of Allyl AcetalsGrad. Sch. Chi Sci. and Eng., Hokkaido Univ.TAKENOUCHI, Yuta;YAMAMOTO, Eiji; OZAKI, Taichi; ITO, Hajime

    1B1-02 Enantioselective Monoborylation of Alkenylsilanes Catalyzed by aChiral Phosphine-Copper(I) ComplexGrad. Sch. Chi Sci. and Eng.,Hokkaido Univ.KUBOTA, Koji; YAMAMOTO, Eiji; ITO, Hajime

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  • 28

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    Al

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    1B1-13 Synthesis and spectroscopic studies of Aluminum porphyrinsUrbanEnvironmental Sci., Tokyo Metropolitan Univ.MATHEW, Siby;KUTTASSERY, Fazalurahman; ONUKI, Satomi; YAMAMOTO, Daisuke;

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    Cu

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    327 13401440

    PC 133013401B1-291B1-29

    17001800 PC 165017001B1-49, 1B1-50, 1B1-51, 1B1-52,

    1B1-53, 1B1-541B1-49 ,- Karan Bobuatong

    1B1-50 N-

    1B1-51

    1B1-52 Cu

    1B1-53

    1B1-54

    328 900 1000

    PC 8509002B1-01, 2B1-02, 2B1-03, 2B1-04,2B1-05, 2B1-06

    2B1-01 //

    2B1-02 - -

    2B1-03 1

    2B1-04

    2B1-05

    2B1-06 Cu(I) 1,2-

    10101110 PC 100010102B1-08, 2B1-10, 2B1-11, 2B1-122B1-08* Copper-Catalyzed Intramolecular Oxidative C(sp3)-H and C(sp2)-HAmidationGrad. Sch. Pharm., The Univ. of Tokyo; The Univ. of TokyoERATO-JSTWANG, Zhen; KUNINOBU, Yoichiro; KANAI, Motomu

    2B1-10 Mizoroki-Heck

    2B1-11 -

    2B1-12*

    11201220 PC 111011202B1-15, 2B1-16, 2B1-17, 2B1-18,

    2B1-19, 2B1-202B1-15

    2B1-16

  • 29

    2B1-17

    2B1-18 C(sp3)-HERATO-JST

    2B1-19

    2B1-20 O-

    328

    Fe

    13301430 PC 132013302B1-28, 2B1-29, 2B1-30, 2B1-322B1-28 CAZBOX

    2B1-29

    2B1-30* Aryl C-Glycoside Synthesis Based on Iron-Catalyzed Cross-CouplingReaction of Arylzinc ReagentsGrad. Sch. Eng., Kyoto Univ.; ICR, KyotoUniv.ADAK, Laksmikanta; KAWAMURA, Shintaro; TOMA, Gabriel; LI,Ho Chuen; TAKENAKA, Toshio; ISOZAKI, Katsuhiro; TAKAYA, Hikaru;

    SHING, Tony K. M.; NAKAMURA, Masaharu

    2B1-32* Iron-Catalyzed Directed Coupling of C(sp2)-H Bond with Organo-boron CompoundsGrad. Sch. Sci., The Univ. of TokyoSHANG, Rui;ILIES, Laurean; NAKAMURA, Eiichi

    14401540 PC 143014402B1-35, 2B1-36, 2B1-37, 2B1-38,

    2B1-39, 2B1-402B1-35 CH

    2B1-36 C-HGHORAI Sujit. K

    2B1-37 GOWER N. J.ADAK Laksmikanta

    2B1-38 /

    2B1-39 Iron-Catalyzed Suzuki-Miyaura Cross-Coupling between Alkyl Ha-lides and Alkynylborate ReagentsICR, Kyoto Univ.; Grad. Sch. Eng.,Kyoto Univ.NAKAGAWA, Naohisa; HATAKEYAMA, Takuji;NAKAMURA, Masaharu

    2B1-40 -NHC

    15501630 PC 154015502B1-42, 2B1-43, 2B1-44, 2B1-452B1-42

    2B1-43

    2B1-44 Grignard

    2B1-45 Grignard

    16401720 PC 163016402B1-47, 2B1-48, 2B1-49, 2B1-502B1-47

    2B1-48

    2B1-49 DMF

    2B1-50 1,6-[2+2+2]

    329

    Zn

    910 1000 PC 9009103B1-02, 3B1-04, 3B1-05, 3B1-063B1-02* Development of Catalytic Allylation Reactions Using Zinc AmidesGrad. Sch. Sci., The Univ. of TokyoYAMASHITA, Yasuhiro; CUI, Yi;KOBAYASHI, Shu

    3B1-04 CUI Yi

    3B1-05 Tunable Zinc Amide-catalyzed Reactions: Selective Synthesis ofAllenylic and Propargylic AlcoholsGrad. Sch. Sci., The Univ. of TokyoXIE, Peizhong; CUI, Yi; YAMASHITA, Yasuhiro; KOBAYASHI, Shu

    3B1-06

    10101110 PC 100010103B1-08, 3B1-09, 3B1-10, 3B1-11,

    3B1-133B1-08

    3B1-09

    Ni

    3B1-10

    3B1-11*

    3B1-13

    11201220 PC 111011203B1-153B1-15

    329

    Cu

    13301430 PC 132013303B1-28, 3B1-31, 3B1-32, 3B1-333B1-28

    Ni

    3B1-31

    3B1-32

    3B1-33

    Cu

    14401540 PC 143014403B1-35, 3B1-36, 3B1-38, 3B1-39,

    3B1-403B1-35 4

    3B1-36* IMRENUS

    3B1-38 1

    3B1-39 2

    3B1-40 (3):

  • 30

    15501650 PC 154015503B1-42, 3B1-43, 3B1-44, 3B1-45,

    3B1-46, 3B1-473B1-42 2

    3B1-43

    3B1-44 (I)

    3B1-45 DMF

    3B1-46

    3B1-47

    17001800 PC 165017003B1-49, 3B1-50, 3B1-51, 3B1-52,

    3B1-53, 3B1-543B1-49

    3B1-50

    3B1-51

    3B1-52 Bis(NHC)-Cu

    3B1-53 1,3-

    3B1-54 ()

    330

    Co

    910 1000 PC 9009104B1-02, 4B1-03, 4B1-054B1-02 N-()

    4B1-03* Co-Catalyzed Cross-Coupling of Alkyl Halides with Tertiary AlkylGrignard Reagents Using a 1,3-Butadiene AdditiveGrad. Sch. Eng., OsakaUniv.; CSIR Indian Institute of Chemical Technology Inorganic andPhysical Chemistry DivisionIWASAKI, Takanori; TAKAGAWA, Hiroaki;SINGH, Surya p.; KUNIYASU, Hitoshi; KAMBE, Nobuaki

    4B1-05* Cobalt-Catalyzed C4-Selective Alkylation of Pyridines and QuinolinesGrad. Sch. Pharm., The Univ. of TokyoYAMAMOTO, Shohei; SAGA,Yutaka; ANDOU, Takashi; MATSUNAGA, Shigeki; KANAI, Motomu

    Ni

    10101110 PC 100010104B1-08, 4B1-09, 4B1-11, 4B1-134B1-08 Ni(0)

    4B1-09*

    4B1-11* Nickel-Catalyzed C-H/C-O Biaryl Coupling: Catalyst Developmentand Mechanistic StudyGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTMUTO, Kei; YAMAGUCHI, Junichiro; ITAMI,Kenichiro

    4B1-13 Ni-Catalyzed Direct Coupling of Carbonyls and Phenol DerivativesGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTTAKISE, Ryosuke; MUTO, Kei; YAMAGUCHI, Junichiro; ITAMI,

    Kenichiro

    11201220 PC 111011204B1-15, 4B1-16, 4B1-17, 4B1-18,

    4B1-19, 4B1-204B1-15 --

    4B1-16 -

    4B1-17 Ni(0)

    4B1-18 Ni(0)

    4B1-19

    4B1-20 N-

    B2 ES103

    G

    327

    10101110 PC 100010101B2-08, 1B2-09, 1B2-10, 1B2-11,

    1B2-121B2-08

    1B2-09

    1B2-10

    1B2-11

    1B2-12*

    11201210 PC 111011201B2-15, 1B2-16, 1B2-17, 1B2-18,

    1B2-191B2-15

    1B2-16

    1B2-17 -

    1B2-18

    1B2-19

    327 14001450

    PC 135014001B2-31, 1B2-32, 1B2-33, 1B2-34,1B2-35

    1B2-31 B12-Ru

    1B2-32

    1B2-33

    1B2-34

    1B2-35 (EGB)

    15001600 PC 145015001B2-37, 1B2-39, 1B2-40, 1B2-41,

    1B2-421B2-37*

    1B2-39 /Ti

    1B2-40 Reductive acylation of phenylacetylene derivatives accompanying withtransposition of the triple bondNagaoka Univ. of Tech.ZHANG,Tianyuan; TAKANO, Atsushi; NISHIYAMA, Yutaro; MAEKAWA,

  • 31

    Hirofumi

    1B2-41

    1B2-42

    328 10101110

    PC 100010102B2-08, 2B2-09, 2B2-10, 2B2-11,2B2-12, 2B2-13

    2B2-08

    2B2-09

    2B2-10 2,3--5,6--p-ALCA, JST

    2B2-11 Mg/Me3SiCl/DMI

    2B2-12 HFIP KF

    2B2-13

    11201220 PC 111011202B2-15, 2B2-17, 2B2-18, 2B2-19,

    2B2-202B2-15* Fabrication of 3D Gradient Polymer Brush Based on BipolarElectrochemistryInterdisciplinary Grad. Sch. Sci. and Eng., Tokyo TechSHIDA, Naoki; FUCHIGAMI, Toshio; TOMITA, Ikuyoshi; INAGI,

    Shinsuke

    2B2-17 [18]

    2B2-18

    2B2-19 2,3--5,6--p-ALCA,JST

    2B2-20

    B3 ESES021

    E

    327

    Si, Mn

    910 1000 PC 9009101B3-02, 1B3-03, 1B3-04, 1B3-05,

    1B3-061B3-02 1,3,6,8-

    1B3-03 -

    1B3-04 WPI-ITbMJST ERATO

    1B3-05 2-

    1B3-06 Endo-Mode Ring Closing Metathesis in Cp Manganese ComplexGrad. Sch. Sci., Osaka Pref. Univ.; CRC, Hokkaido Univ.TSENG, Ya-yi;KAMIKAWA, Ken; TAKAHASHI, Tamotsu; OGASAWARA, Masamichi

    Cr, Re

    10101110 PC 100010101B3-08, 1B3-10, 1B3-12, 1B3-131B3-08* Catalytic Enantioselective Synthesis of Planar-Chiral (-Arene)chromium Complexes by Mo-Catalyzed Ring-Closing MetathesisCRC,

    Hokkaido Univ.; Grad. Sch. Sci., Osaka Pref. Univ.WU, Wei-yi; TSENG,Ya-yi; ARAE, Sachie; NAKAMURA, Chihiro; MORITA, Tomotaka;

    TAKAHASHI, Tamotsu; OGASAWARA, Masamichi; KAMIKAWA, Ken

    1B3-10* C-HCREST-JST

    1B3-12 C(sp3)-H

    1B3-13 --

    Re, Ru

    11201220 PC 111011201B3-15, 1B3-16, 1B3-17, 1B3-18,

    1B3-19, 1B3-201B3-15 Markovnikov

    1B3-16

    1B3-17

    1B3-18 /

    1B3-19

    1B3-20 /

    327

    Ru

    13401440 PC 133013401B3-29, 1B3-30, 1B3-31, 1B3-32,

    1B3-33, 1B3-341B3-29 Ru()-Pheox-Chanthamath Soda

    1B3-30 -

    1B3-31 7-

    1B3-32 C-C

    1B3-33

    1B3-34

    17001800 PC 165017001B3-49, 1B3-51, 1B3-52, 1B3-531B3-49*

    1B3-51

    1B3-52

    1B3-53* Syntheses and Reactivities of Hydrido Carbonyl Ruthenium Com-plexes Bearing Various TriarylphosphinesFac. Sci. Tech., Keio Univ.OGIWARA, Yohei; KOCHI, Takuya; KAKIUCHI, Fumitoshi

    328

    Au

    920 1010 PC 9109202B3-03, 2B3-04, 2B3-05, 2B3-06,

    2B3-072B3-03

  • 32

    2B3-04 Nanoporous gold as a highly active catalyst for aerobic oxidation ofhydroxylamines into nitronesGrad. Sch. Sci., Tohoku Univ.KUSUMA,Indra; YUDHA, Salprima; ASAO, Naoki

    2B3-05

    Ag

    2B3-06

    Ni

    2B3-07 Ni() N-

    10201110 PC 101010202B3-09, 2B3-10, 2B3-11, 2B3-12,

    2B3-132B3-09

    2B3-10 3

    2B3-11

    2B3-12

    2B3-13

    Co

    11201220 PC 111011202B3-15, 2B3-16, 2B3-17, 2B3-182B3-15 N-

    2B3-16 o

    2B3-17

    2B3-18 Development of Cobalt-Catalyzed C-H BondFunctionalization ReactionsNanyang Tech. Univ.YOSHIKAI, Naohiko

    328

    Pt

    13301430 PC 132013302B3-28, 2B3-29, 2B3-30, 2B3-31,

    2B3-32, 2B3-332B3-28 PSiN--

    2B3-29 (II)

    2B3-30

    Rh

    2B3-31 - 1,6-[3.1.0]

    2B3-32 (III)

    2B3-33 (I) 1,2-2-

    14401540 PC 143014402B3-35, 2B3-36, 2B3-37, 2B3-38,

    2B3-39, 2B3-402B3-35 2,3-/

    2B3-36 3--1,2-

    2B3-37 [2+2+2]

    2B3-38 ,-[2+2+2]

    2B3-39 5-[2+2+2]

    2B3-40

    15501650 PC 154015502B3-42, 2B3-43, 2B3-44, 2B3-45,

    2B3-46, 2B3-472B3-42 -5(4H)-

    2B3-43 [2+2+2]

    2B3-44 C-H

    2B3-45

    2B3-46 CO-C

    2B3-47

    17001730 PC 165017002B3-49, 2B3-50, 2B3-512B3-49

    2B3-50

    2B3-51 3-

    329

    Ti, Nb

    900 1000 PC 8509003B3-01, 3B3-02, 3B3-03, 3B3-04,

    3B3-05, 3B3-063B3-01

    3B3-02

    3B3-03

    3B3-04 NbCl5

    3B3-05

    3B3-06 Nb

    V, Bi, Te, Ga

    10101110 PC 100010103B3-08, 3B3-09, 3B3-10, 3B3-11,

    3B3-12, 3B3-133B3-08 5

    3B3-09 (V)JST

    3B3-10

    3B3-11

    3B3-12

    3B3-13 Three-component Reaction of Esters with Silyl Cyanide and KeteneSilyl Acetals Catalyzed by Gallium TrihalidesGrad. Sch. Eng., Osaka

  • 33

    Univ.INAMOTO, Yoshihiro; KAGA, Yuta; NISHIMOTO, Yoshihiro;YASUDA, Makoto; BABA, Akio

    In

    11201220 PC 111011203B3-15, 3B3-16, 3B3-17, 3B3-18,

    3B3-19, 3B3-203B3-15 -[2+2]

    3B3-16

    3B3-17

    3B3-18

    3B3-19 -

    3B3-20

    329

    Rh

    13301430 PC 132013303B3-28, 3B3-29, 3B3-30, 3B3-31,

    3B3-32, 3B3-333B3-28 (III)[2 + 2 + 2]

    3B3-29

    3B3-30 Rh(I)-Catalyzed Arylative Double-Carbonylation of Alkynes withArylboronic Acids Using Formaldehyde as a CO SourceGrad. Sch. Mat.Sci., NAISTMORIMOTO, Tsumoru; WANG, Chuang; KAKIUCHI,Kiyomi; ARTOK, Levent

    3B3-31

    3B3-32 3

    3B3-33 --,-

    14401540 PC 143014403B3-35, 3B3-37, 3B3-38, 3B3-393B3-35*

    3B3-37 1,2

    3B3-38 sp2sp3

    3B3-39*

    15501650 PC 154015503B3-42, 3B3-43, 3B3-44, 3B3-45,

    3B3-46, 3B3-473B3-42 N---

    3B3-43 ,- 2,3-

    3B3-44 2,5-

    3B3-45 1--3-(2-)

    3B3-46 3-

    3B3-47

    17001740 PC 165017003B3-49, 3B3-50, 3B3-51, 3B3-523B3-49

    3B3-50

    3B3-51 Ge-H C-H

    3B3-52

    330

    Sr

    910 1000 PC 9009104B3-02, 4B3-03, 4B3-04, 4B3-05,

    4B3-064B3-02

    4B3-03 Grignard

    4B3-04

    Ba

    4B3-05 -

    Y

    4B3-06 4

    Sc

    10101110 PC 100010104B3-08, 4B3-10, 4B3-12, 4B3-134B3-08* Sc(OTf)3

    4B3-10* Scandium-Catalyzed Enantioselective C-H Alkylation of PyridinesRIKEN Organometallic Chemistry LabSONG, Guoyong; HOU,Zhaomin

    Sn

    4B3-12

    4B3-13

    B4 ESES022

    E

    327

    Pd

    900 1000 PC 8509001B4-01, 1B4-03, 1B4-04, 1B4-051B4-01* Palladium-catalyzed One-shot Aromatic -Extension of PolycyclicAromatic HydrocarbonsGrad. Sch. Sci., Nagoya Univ.; Nagoya Univ. WPI-ITbM; ERATO, JSTOZAKI, Kyohei; KAWASUMI, Katsuaki; ITO,Hideto; ITAMI, Kenichiro

    1B4-03 2- C-H C-NWPI-ITbMJST ERATO

    1B4-04 1,n-/

    1B4-05* Synthesis of Cyclic Compounds by Cycloisomerization of Various 1,n-Dienes via Chain WalkingFac. Sci. Tech., Keio Univ.HAMASAKI, Taro;KAKIUCHI, Fumitoshi; KOCHI, Takuya

  • 34

    10101110 PC 100010101B4-08, 1B4-09, 1B4-11, 1B4-131B4-08 C-H/C-HERATO-JST

    1B4-09* -

    1B4-11* -

    1B4-13 C-

    11201220 PC 111011201B4-15, 1B4-16, 1B4-18, 1B4-201B4-15

    1B4-16* Palladium-Catalyzed Regioselective C-H Fluorosilylation of 2-Phe-nylpyridines: Synthesis of Silafluorene EquivalentsGrad. Sch. Pharm., TheUniv. of Tokyo; The Univ. of Tokyo ERATO-JSTXIAO, Qing; MENG,Xiangtai; KANAI, Motomu; KUNINOBU, Yoichiro

    1B4-18* Palladium-catalyzed Silylation and Germanylation of C(sp2)-H and C(sp3)-H BondsGrad. Sch. Pharm., The Univ. of TokyoKANYIVA,Stephen-kyalo; KUNINOBU, Yoichiro; KANAI, Motomu

    1B4-20 [1,2-b:8,7-b]JSTACT-C

    327

    Rh

    13401440 PC 133013401B4-29, 1B4-321B4-29

    Pd

    1B4-32

    17001800 PC 165017001B4-49, 1B4-50, 1B4-51, 1B4-52,

    1B4-53, 1B4-541B4-49 Pd 1

    1B4-50

    1B4-51

    1B4-52 Pd

    1B4-53

    1B4-54 C-H 5

    328

    Ir

    900 1000 PC 8509002B4-01, 2B4-02, 2B4-03, 2B4-04,

    2B4-05, 2B4-062B4-01 1,3-

    2B4-02 - 1,3-

    2B4-03

    2B4-04 C-H 1,3-[3 + 2]

    2B4-05 C-H[3 + 2]

    2B4-06

    10101110 PC 100010102B4-08, 2B4-09, 2B4-10, 2B4-12,

    2B4-132B4-08 C-H

    2B4-09 C-H

    2B4-10* /Me-BIPAM-

    2B4-12 Synthesis of Triarylboranes via Iridium-Catalyzed C-H BorylationGrad. Fac. Eng., Hokkaido Univ.SASAKI, Ikuo; ISHIYAMA, Tatsuo;ITOU, Hajime

    2B4-13 C-H WPI-ITbMJST ERATO

    11201220 PC 111011202B4-15, 2B4-16, 2B4-182B4-15 Ir(III)-PNP

    2B4-16* Syntheisis and Catalytic Function of Hydroxycyclopentadienyl Iri-dium ComplexGrad. Sch. Eng., The Univ. of TokyoKUSUMOTO,Shuhei; AKIYAMA, Midori; NOZAKI, Kyoko

    2B4-18

    328

    Pd

    13301430 PC 132013302B4-28, 2B4-30, 2B4-31, 2B4-32,

    2B4-332B4-28* Modular Synthesis of Triarylmethanes through Palladium-CatalyzedSequential Arylation of Methyl Phenyl SulfoneWPI-ITbM, Nagoya Univ.NAMBO, Masakazu; CRUDDEN, Cathleen M.

    2B4-30 -

    2B4-31 Pd--

    2B4-32 Synthetic Applications of-(Acylamino)alkylboronic Esters: Controlof Stereochemical Course in Catalytic Construction of Stereogenic Carbon

    CentersGrad. Sch. Eng., Kyoto Univ.OHMURA, Toshimichi; MIWA,Kyoko; SUGINOME, Michinori

    2B4-33 C1

    14401540 PC 143014402B4-35, 2B4-36, 2B4-37, 2B4-38,

    2B4-39, 2B4-402B4-35

    2B4-36 -

    2B4-37 NHC/Pd 2-2-

    2B4-38 Pd 2-

    2B4-39 PdWPI-AIMR

    2B4-40 NHC -

    15501650 PC 154015502B4-42, 2B4-43, 2B4-44, 2B4-45,

    2B4-46, 2B4-472B4-42

  • 35

    2B4-43 HOMSi

    2B4-44 - HOMSi

    2B4-45

    2B4-46 2- Pd

    2B4-47

    17001730 PC 165017002B4-49, 2B4-50, 2B4-512B4-49 Synthesis of Methoxy-Substituted Picenes and Eects of TheirPosition on Single Crystal StructuresGrad. Sch. Nat. Sci. Technol.,Okayama Univ.; Aichi Univ. of Educ. Dept. of Chem.; JST ACT-CCHEN, Xi-chao; CHANG, Ning-hui; MORI, Hiroki; NAKAJIMA, Kiyohiko;

    NISHIHARA, Yasushi

    2B4-50

    2B4-51 Giese

    329 900 1000

    PC 8509003B4-01, 3B4-02, 3B4-03, 3B4-04,3B4-05, 3B4-06

    3B4-01 DMF Pd 2,3-

    3B4-02 -5(4H)-

    3B4-03 An Improvement of Palladium Catalyst for the [4+2] Cycloadditionof o-(Silylmethyl)benzyl Carbonate with AlkenesFac. Sci., Kyushu Univ.JIN, Yushu; ISHIZUKA, Kentaro; KUWANO, Ryoichi

    3B4-04

    3B4-05

    3B4-06

    10101110 PC 100010103B4-08, 3B4-09, 3B4-10, 3B4-11,

    3B4-12, 3B4-133B4-08

    3B4-09

    3B4-10 t-

    3B4-11 SPRIX

    3B4-12

    3B4-13 FAN Lulu

    11201220 PC 111011203B4-15, 3B4-16, 3B4-17, 3B4-193B4-15 Pd P-CP-

    3B4-16 Pd 3

    3B4-17* PQXphos

    3B4-19* Quantication of steric inuence in palladium/alkylphosphine-sulfo-nate catalystsGrad. Sch. Eng., The Univ. of TokyoOTA, Yusuke; ITO,Shingo; NOZAKI, Kyoko

    329

    Pd, Ir

    13301430 PC 132013303B4-28, 3B4-29, 3B4-30, 3B4-31,

    3B4-323B4-28 31

    3B4-29 3

    3B4-30

    3B4-31 Hydrothioalkylation of Electron-Decient Alkenes by PhotoredoxCatalysisChem. Res. Lab., Tokyo TechLI, Yanjie; MIYAZAWA, Kazuki;KOIKE, Takashi; AKITA, Munetaka

    3B4-32* (HCOOH) MUCKERMAN James

    Ir

    14401540 PC 143014403B4-35, 3B4-36, 3B4-37, 3B4-38,

    3B4-39, 3B4-403B4-35 Ir

    3B4-36 2

    3B4-37

    3B4-38

    3B4-39 C-H

    3B4-40

    15501650 PC 154015503B4-42, 3B4-43, 3B4-44, 3B4-45,

    3B4-46, 3B4-473B4-42 Utility of a Trimethylsilyl Group as an Equivalent of HydroxylGroup: Synthesis of Alkanols via Iridium-Catalyzed C(sp3)-H Borylation

    Grad. Sch. Eng., Kyoto Univ.OHMURA, Toshimichi; TORIGOE,Takeru; SUGINOME, Michinori

    3B4-43

    3B4-44

    3B4-45 ,[2+2+2]

    3B4-46

    3B4-47

    17001800 PC 165017003B4-49, 3B4-50, 3B4-51, 3B4-52,

    3B4-53, 3B4-543B4-49 3 2 7 C-H

    3B4-50 1 7-

    3B4-51 C(sp3)-H

    3B4-52 C-H

    3B4-53

    3B4-54 C-H-

  • 36

    330

    Pd

    900 1000 PC 8509004B4-01, 4B4-02, 4B4-03, 4B4-04,

    4B4-054B4-01 Pd-Catalyzed Cascade Crossover Annulation of o-Alkynylarylhalidesand Diarylacetylenes Leading to Dibenzo[a,e]pentalenesWPI-AIMR,Tohoku Univ.ZHAO, Jian; ONIWA, Kazuaki; ASAO, Naoki;YAMAMOTO, Yoshinori; JIN, Tienan

    4B4-02

    4B4-03 2-

    4B4-04 Enantioselective Palladium(II) Catalyzed Cyclization-CycloadditionCascade ReactionsISIR, Osaka Univ.ABOZEID , Mohamed;TAKIZAWA, Shinobu; SASAI, Hiroaki

    4B4-05*

    10101110 PC 100010104B4-08, 4B4-10, 4B4-11, 4B4-124B4-08* /

    4B4-10 /

    4B4-11 WPI-ITbMJST ERATO

    4B4-12* o-- o-JSTACT-C

    11201220 PC 111011204B4-15, 4B4-16, 4B4-17, 4B4-18,

    4B4-19, 4B4-204B4-15 PCPPd

    4B4-16

    4B4-17

    4B4-18

    4B4-19 PGeP-Palladium Complex-Catalyzed Hydrocarboxylation of Alleneswith FormateGrad. Sch. Sci., Eng., Tokyo TechZHU, Chuan; SASANO,Kota; TAKAYA, Jun; IWASAWA, Nobuharu

    4B4-20

    B5 ESES024

    D

    327

    900 1000 PC 8509001B5-01, 1B5-02, 1B5-03, 1B5-04,

    1B5-05, 1B5-061B5-01 4

    1B5-02 2 5--

    1B5-03 1,14:7,8-Bis(dithio)-6,13-dithiopentacenequinone

    1B5-04

    1B5-05 D--A 1,4--1,3-

    1B5-06

    10101110 PC 100010101B5-08, 1B5-09, 1B5-10, 1B5-11,

    1B5-12, 1B5-131B5-08 1B5-09

    1B5-10 [4]

    1B5-11 (5--2-)-1- 1,1-

    1B5-12 2,4,6-(2-)-1,3,5-

    1B5-13 (p-)

    11201220 PC 111011201B5-15, 1B5-16, 1B5-17, 1B5-18,

    1B5-19, 1B5-201B5-15 1-

    1B5-16

    1B5-17

    1B5-18

    1B5-19

    1B5-20 1,3-

    327 13301430

    PC 132013301B5-28, 1B5-29, 1B5-30, 1B5-31,1B5-32, 1B5-33

    1B5-28 Brnsted acid-catalyzed selective hydroboration of alkynylboronatesWPI-AIMR, Tohoku Univ.HO, Hon eong; ASAO, Naoki;YAMAMOTO, Yoshinori; JIN, Tienan

    1B5-29 1B5-30

    1B5-31 Rind(6)

    1B5-32 diborane(4)

    1B5-33

    14401540 PC 143014401B5-35, 1B5-36, 1B5-37, 1B5-38,

    1B5-39, 1B5-401B5-35

    1B5-36 o-

    1B5-37

    1B5-38

    1B5-39

    1B5-40 Reaction of boryl metal species with dihydrogenGrad. Sch. Eng.,The Univ. of Tokyo; Fac. Sci. Eng., Chuo Univ.ARAMAKI, Yoshitaka;ZHAO, Xiaoxi; YAMASHITA, Makoto; NOZAKI, Kyoko

    15501650 PC 154015501B5-42, 1B5-43, 1B5-44, 1B5-45,

    1B5-46, 1B5-471B5-42

    1B5-43

  • 37

    1B5-44 2,4,6--t- CH

    1B5-45 -

    1B5-46

    1B5-47

    17001750 PC 165017001B5-49, 1B5-50, 1B5-51, 1B5-52,

    1B5-531B5-49 2- 2-

    1B5-50

    1B5-51 One-Pot

    1B5-52

    1B5-53

    328 900 1000

    PC 8509002B5-01, 2B5-02, 2B5-03, 2B5-04,2B5-05, 2B5-06

    2B5-01

    2B5-02 5

    2B5-03 5

    2B5-04

    2B5-05 4,8-[1,2-d:4,5-d][1,2,3]/

    2B5-06

    10101110 PC 100010102B5-08, 2B5-09, 2B5-10, 2B5-11,

    2B5-12, 2B5-132B5-08 [7]

    2B5-09 : Wagner-Meerwein

    2B5-10 12

    2B5-11 buta-1,3-diy-nylbenzene

    2B5-12

    2B5-13 S-

    11201220 PC 111011202B5-15, 2B5-16, 2B5-17, 2B5-18,

    2B5-19, 2B5-202B5-15

    2B5-16 BowlN-

    2B5-17 Bowl

    2B5-18 Ch(IV)=C=S(VI) (Ch = S, Se)

    2B5-19

    2B5-20

    328 13301430

    PC 132013302B5-28, 2B5-29, 2B5-30, 2B5-31,2B5-32, 2B5-33

    2B5-28

    2B5-29 2-(R)-(+)-

    2B5-30 Pd/C

    2B5-31 trans--

    2B5-32

    2B5-33

    14401540 PC 143014402B5-35, 2B5-36, 2B5-37, 2B5-38,

    2B5-39, 2B5-402B5-35

    2B5-36 1--1,3- Diels-Alder

    2B5-37 Rind

    2B5-38 [3] 6

    2B5-39

    2B5-40 3

    15501640 PC 154015502B5-42, 2B5-43, 2B5-44, 2B5-45,

    2B5-462B5-42 8

    2B5-43

    2B5-44

    2B5-45 JST-ERATO

    2B5-46 9-

    16501730 PC 164016502B5-48, 2B5-49, 2B5-50, 2B5-512B5-48 Wittig

    2B5-49 6 Ph6Te

    2B5-50 6

    2B5-51 6 AIM

    329 13201350

    PC 131013203B5-27, 3B5-28, 3B5-293B5-27 1- 4,7-[b]

    3B5-28

    3B5-29 [2.2.2]

    14001440 PC 135014003B5-31, 3B5-32, 3B5-333B5-31

    3B5-32

  • 38

    3B5-33*

    16501730 PC 164016503B5-48, 3B5-503B5-48* Ni / B(C6F5)3 Catalyst System for Highly Selective Crossed-Esterication of Triuoromethylketones with AldehydesGrad. Sch. Eng.,Osaka Univ.DOI, Ryohei; OHASHI, Masato; OGOSHI, Sensuke

    3B5-50*

    17401820 PC 173017403B5-53, 3B5-553B5-53* 1--1,3-

    3B5-55* Synthetic Studies on Organoselenium-substituted Phosphenium Ca-tionsICR, Kyoto Univ.SUGAMATA, Koh; VILLALBA FRANCO, Josemanuel; SASAMORI, Takahiro; TOKITOH, Norihiro

    B6 ESES025

    A

    327

    900 1000 PC 8509001B6-01, 1B6-02, 1B6-03, 1B6-04,

    1B6-05, 1B6-061B6-01 1,3- aza Diels-Alder

    1B6-02 hetero Diels-Alder

    1B6-03 2--

    1B6-04 1 2 3,3-

    1B6-05 -Pictet-SpenglerPark JiHyun

    1B6-06 Friedel-Crafts

    10101110 PC 100010101B6-08, 1B6-09, 1B6-10, 1B6-11,

    1B6-12, 1B6-131B6-08 MannichRAHAMAN Hasibur

    1B6-09

    1B6-10 -

    1B6-11 NicholasLI Feng

    1B6-12

    1B6-13 Mannich

    11201220 PC 111011201B6-15, 1B6-16, 1B6-17, 1B6-19,

    1B6-201B6-15 3,3--1,1--2,2-

    1B6-16

    1B6-17*

    1B6-19

    1B6-20

    327 13301430

    PC 132013301B6-28, 1B6-30, 1B6-31, 1B6-32,1B6-33

    1B6-28* Copolymerization of carbon dioxide and dienes via lactone inter-mediateGrad. Sch. Eng., The Univ. of TokyoNAKANO, Ryo; ITO,Shingo; NOZAKI, Kyoko

    1B6-30 1

    1B6-31 2

    1B6-32 YOOWoo-Jin

    1B6-33 An Ecient Synthesis of Isocoumarins via N-Heterocyclic Carbene-Copper Complex Catalyzed Three-Component Coupling Reactions of Ben-

    zynes, Terminal Alkynes, and Carbon DioxideGrad. Sch. Sci., The Univ. ofTokyoNGUYEN VU QUANG, Thanh; YOO, Woo-Jin; KOBAYASHI,Shu

    14401540 PC 143014401B6-35, 1B6-37, 1B6-38, 1B6-39,

    1B6-401B6-35* -

    1B6-37 ,-(II)

  • 39

    1B6-38 FooSiong Wan

    1B6-39 JST

    1B6-40 1- SmI2 Zn

    15501650 PC 154015501B6-42, 1B6-43, 1B6-44, 1B6-45,

    1B6-46, 1B6-471B6-42 - (E)--[3+2]: Lectard Sylvain

    1B6-43

    1B6-44 //

    1B6-45 SOD

    1B6-46 (I)-

    1B6-47 CH I2CNER

    17001800 PC 165017001B6-49, 1B6-51, 1B6-52, 1B6-53,

    1B6-541B6-49* Catalytic Hydrogenation of Carboxamides Using Ru ComplexBearing Tetradentate LigandGrad. Sch. Sci., Nagoya Univ.MIURA,Takashi; NARUTO, Masayuki; NOYORI, Ryoji; SAITO, Susumu

    1B6-51

    1B6-52

    1B6-53

    1B6-54

    18101850 PC 180018101B6-56, 1B6-57, 1B6-581B6-56 //

    1B6-57

    1B6-58* --,-

    328 900 1000

    PC 8509002B6-01, 2B6-02, 2B6-03, 2B6-04,2B6-05

    2B6-01

    2B6-02 - Friedel-Crafts

    2B6-03 C1- DielsAlder

    2B6-04 Diels-Alder

    2B6-05* - Diels-Alder

    10101110 PC 100010102B6-08, 2B6-09, 2B6-10, 2B6-11,

    2B6-132B6-08

    2B6-09 1,3-

    2B6-10

    2B6-11* Petasis-FerrierGRIDNEV Ilya

    2B6-13

    11201220 PC 111011202B6-15, 2B6-17, 2B6-18, 2B6-19,

    2B6-202B6-15* Site-Selective Aerobic Oxygenation of sp3 C-H Bonds of AlcoholsCovalently Bound to N-Oxyl Radical ActivatorGrad. Sch. Pharm., TheUniv. of TokyoOISAKI, Kounosuke; OZAWA, Jun; NI, Jizhi; TASHIRO,Masayuki; KANAI, Motomu

    2B6-17

    2B6-18 TMSNCS Nadaf Rashid Nabisaheb

    2B6-19 1,5-

    2B6-20

    328 13301430

    PC 132013302B6-28, 2B6-31, 2B6-32, 2B6-332B6-28 WPI-ITbM

    2B6-31 Diels-Alder

    2B6-32 Phase-transfer catalyzed asymmetric synthesis of 5,5-disubstitutedunsaturated -lactamsGrad. Sch. Sci., Kyoto Univ.ARLT, Alexander;HASHIMOTO, Takuya; MARUOKA, Keiji

    2B6-33

    14401540 PC 143014402B6-35, 2B6-37, 2B6-38, 2B6-392B6-35* N

    2B6-37 2WPI-ITbMJST CREST

    2B6-38 1,6- WPI-ITbMJST CREST

    2B6-39* WPI-ITbMJST CREST

    15501650 PC 154015502B6-42, 2B6-44, 2B6-45, 2B6-46,

    2B6-472B6-42* 1,2-- Diels-AlderJST CREST

    2B6-44 -JST CREST

    2B6-45 Boronic Acid-DMAP(O) Cooperative Catalysis for DehydrativeCondensation between Carboxylic Acids and AminesGrad. Sch. Eng.,Nagoya Univ.LU, Yanhui; ISHIHARA, Kazuaki

    2B6-46 (II)

    2B6-47 Asymmetric catalytic activity of quaternary ammonium salts ofcinchona alkaloid containing acetylenic moietyToyohashi Univ. of Tech.HASSAN, Md. mehadi; HARAGUCHI, Naoki; ITSUNO, Shiniti

  • 40

    17001730 PC 165017002B6-49, 2B6-512B6-49*

    2B6-51

    329 900 1000

    PC 8509003B6-01, 3B6-02, 3B6-03, 3B6-04,3B6-05, 3B6-06

    3B6-01 1,2,3- 2,2- WPI-ITbMJST CREST

    3B6-02 3-WPI-ITbMJST CREST

    3B6-03 WPI-ITbMJST CREST

    3B6-04

    3B6-05 Morita-Baylis-Hillman

    3B6-06 Baylis-Hillman

    10101110 PC 100010103B6-08, 3B6-09, 3B6-10, 3B6-11,

    3B6-123B6-08 3B6-09

    3B6-10 /PPY:

    3B6-11 MacMillan

    3B6-12* Development of Catalytic Imine-imine Cross Coupling ReactionsGrad. Sch. Sci., The Univ. of TokyoMATSUMOTO, Masatoshi;HARADA, Masashi; YAMASHITA, Yasuhiro; KOBAYASHI, Shu

    11201220 PC 111011203B6-15, 3B6-17, 3B6-18, 3B6-203B6-15* 3B6-17 -

    3B6-18* N-Heterocyclic Carbene Catalyzed Umpolung of Michael AcceptorsNagoya Inst. of Tech. Department of Materials Science and EngineeringMATSUOKA, Shin-ichi; KATO, Terumasa; NAMERA, Shoko;

    NAKAZAWA, Masanori; TAKAGI, Koji; SUZUKI, Masato

    3B6-20 N-

    329 16501740

    PC 164016503B6-48, 3B6-49, 3B6-50, 3B6-51,3B6-52

    3B6-48 Phospha-Brook--

    3B6-49 Phospha-Brook

    3B6-50 Lossen

    3B6-51

    3B6-52 -

    17501830 PC 174017503B6-54, 3B6-55, 3B6-56, 3B6-573B6-54

    3B6-55 - N- Claisen

    3B6-56

    3B6-57 HMPT CFBr3

    ERATO-JST

    B7 ESES033

    A

    327

    900 1000 PC 8509001B7-01, 1B7-03, 1B7-04, 1B7-05,

    1B7-061B7-01* -- 1,3-JST CREST

    1B7-03 n-- Diels-AlderJST CREST

    1B7-04

    1B7-05 DielsAlder

    1B7-06

    10101110 PC 100010101B7-08, 1B7-10, 1B7-11, 1B7-12,

    1B7-131B7-08*

    1B7-10

    1B7-11

    1B7-12 2-

    1B7-13

    11201220 PC 111011201B7-15, 1B7-16, 1B7-17, 1B7-18,

    1B7-19, 1B7-201B7-15

    1B7-16

    1B7-17 2,2,3-Trimethyl-2-silapent-4-ene

    1B7-18 Felkin-Anh()

    1B7-19 5-oxa-8-thiaspiro[3.4]oct-1-ene

    1B7-20 Nazarov

    327 13301430

    PC 132013301B7-28, 1B7-29, 1B7-30, 1B7-31,1B7-33

    1B7-28 -

    1B7-29

    1B7-30 JST CRESTUYANIK Muhammet

    1B7-31* 2- JST CREST UYANIK

  • 41

    Muhammet1B7-33 JST CRESTUYANIKMuhammet

    14401540 PC 143014401B7-35, 1B7-37, 1B7-38, 1B7-39,

    1B7-401B7-35* ortho-/1,4-/ I2CNER

    1B7-37 (III)ortho-JST CRESTUYANIK Muhammet

    1B7-38 (III) 2,5-JST CRESTUYANIK Muhammet

    1B7-39 (III) 1,5-

    1B7-40 Baeyer-Villiger

    UYANIK Muhammet15501650 PC 154015501B7-42, 1B7-43, 1B7-44, 1B7-45,

    1B7-471B7-42 [3+2]

    1B7-43 -

    1B7-44

    1B7-45* Dehydrogenation of primary alcohols using metal oxide photocata-lysts under visible light irradiationRCMS, Nagoya Univ.; Grad. Sch. Sci.,Nagoya Univ.; Inst. Adv. Res., Nagoya Univ.; Fac. Sci., Tokyo Univ. of Sci.NAKA, Hiroshi; LIU, Zijun; CANER, Joaquim; KUDO, Akihiko; NOYORI,

    Ryoji; SAITO, Susumu

    1B7-47

    17001740 PC 165017001B7-49, 1B7-50, 1B7-51, 1B7-521B7-49 Visible Light-Mediated Chan-Lam Coupling Reactions of Arylboro-nic Acids and AminesGrad. Sch. Sci., The Univ. of TokyoYOO, Woo-Jin;TSUKAMOTO, Tatsuhiro; KOBAYASHI, Shu

    1B7-50 YOO Woo-Jin

    1B7-51

    1B7-52

    17501830 PC 174017501B7-54, 1B7-55, 1B7-56, 1B7-571B7-54 -

    1B7-55 -

    1B7-56 C-1 JACQUET AntoineROBERT FredericLANDAIS Yannick

    1B7-57

    328 900 1000

    PC 8509002B7-01, 2B7-02, 2B7-03, 2B7-04,2B7-05, 2B7-06

    2B7-01

    2B7-02 YOO Woo-Jin

    2B7-03

    2B7-04 (V) Oxone

    1 ,2-JSTCRESTUYANIK Muhammet

    2B7-05 /JST CRESTUYANIK Muhammet

    2B7-06 --JST CRESTUYANIK Muhammet

    UYANIK Muhammet10101110 PC 100010102B7-08, 2B7-09, 2B7-10, 2B7-11,

    2B7-12, 2B7-132B7-08

    2B7-09 C(sp3)-H

    2B7-10 1,3-

    2B7-11 SmI2/Sm/Me3SiCl

    2B7-12

    2B7-13

    11201210 PC 111011202B7-15, 2B7-16, 2B7-17, 2B7-18,

    2B7-192B7-15 C-H/C-C

    2B7-16 p-I-PhOH

    2B7-17 BH3 SN2

    2B7-18

    2B7-19 WPI-AIMR

    328 13301430

    PC 132013302B7-28, 2B7-29, 2B7-30, 2B7-31,2B7-32, 2B7-33

    2B7-28 LASC-SWNT

    2B7-29 Lewis-(LASC)

    2B7-30

    2B7-31 (II)Mannich Diels-Alder

    2B7-32 Diels-Alder

    2B7-33 - 1,2- DielsAlderJST CREST

    14401540 PC 143014402B7-35, 2B7-37, 2B7-38, 2B7-39,

    2B7-402B7-35* Study of heterogeneous organic reactions using real-time reactionmonitoring with mass spectrometryGrad. Sch. Sci., The Univ. of TokyoMASUDA, Koichiro; KOBAYASHI, Shu

    2B7-37

    2B7-38 2,23 2,42

    2B7-39 --,-

    2B7-40 Lewis

  • 42

    15501650 PC 154015502B7-42, 2B7-43, 2B7-44, 2B7-46,

    2B7-472B7-42 (II)

    2B7-43 Cu(II) catalysis in asymmetric boron conjugate additions in organicsolventsGrad. Sch. Sci., The Univ. of TokyoZHU, Lei; KITANOSONO,Taku; XU, Pengyu; KOBAYASHI, Shu

    2B7-44* Stereoselective synthesis of densely heterofunctionalized molecules bysecondary amine catalystsGrad. Sch. Sci., Kyoto Univ.SAKAMOTO,Ryu; KANO, Taichi; MARUOKA, Keiji

    2B7-46 ,

    2B7-47

    17001730 PC 165017002B7-49, 2B7-50, 2B7-512B7-49

    2B7-50 PyBidine aza-Henry

    2B7-51 NHC,-

    329 900 1000

    PC 8509003B7-01, 3B7-02, 3B7-03, 3B7-04,3B7-05, 3B7-06

    3B7-01 N-Mannich

    3B7-02

    3B7-03

    3B7-04 /()

    3B7-05

    3B7-06 2-

    10101110 PC 100010103B7-08, 3B7-09, 3B7-10, 3B7-11,

    3B7-12, 3B7-133B7-08

    3B7-09 1,4-

    3B7-10 1,4-

    3B7-11 2(3H)- antinitro-Michael

    3B7-12

    3B7-13 [2+2]

    11201210 PC 111011203B7-15, 3B7-16, 3B7-17, 3B7-183B7-15 2-

    3B7-16 - N-/Mi-chael

    3B7-17 Michael

    3B7-18* (III) 1,4-

    329 17001740

    PC 165017003B7-49, 3B7-50, 3B7-51, 3B7-523B7-49

    3B7-50

    3B7-51 (1,10)

    3B7-52

    17501830 PC 174017503B7-54, 3B7-55, 3B7-56, 3B7-573B7-54

    3B7-55

    3B7-56 Julia

    3B7-57

    B8 ESES034

    A

    327

    900 1000 PC 8509001B8-01, 1B8-02, 1B8-03, 1B8-04,

    1B8-051B8-01

    1B8-02 1,2-JST ERATO

    1B8-03

    1B8-04

    1B8-05* JST ERATO

    10101110 PC 100010101B8-08, 1B8-09, 1B8-10, 1B8-11,

    1B8-12, 1B8-131B8-08 Claisen CF3

    1B8-09

    1B8-10 redox

    1B8-11 4,4,4--2--1-

    1B8-12 1--1-

    1B8-13 Gem-

    11201220 PC 111011201B8-15, 1B8-16, 1B8-17, 1B8-18,

    1B8-19, 1B8-201B8-15

    1B8-16 (-)

  • 43

    1B8-17

    1B8-18 sp3

    1B8-19

    1B8-20 2,3,3,3-

    327 13301430

    PC 132013301B8-28, 1B8-29, 1B8-30, 1B8-32,1B8-33

    1B8-28 3,3-

    1B8-29 C-F

    1B8-30* HF

    1B8-32 -

    1B8-33

    14401540 PC 143014401B8-35, 1B8-36, 1B8-37, 1B8-38,

    1B8-39, 1B8-401B8-35

    1B8-36 SN2-SNV

    1B8-37 JST CREST

    1B8-38 (III) 2-JST CREST

    1B8-39

    1B8-40

    15501650 PC 154015501B8-42, 1B8-43, 1B8-451B8-42 -[3+2] 3-(-3-)-

    1B8-43* Catalytic asymmetric [3+2] cycloaddition for indole compoundscontaining quaternary chiral carbon centerGrad. Sch. Sci., Chiba Univ.AWATA, Atsuko; ARAI, Takayoshi

    1B8-45

    17001740 PC 165017001B8-49, 1B8-51, 1B8-521B8-49* WPI-ITbMJST CREST

    1B8-51 5-[3+2]WPI-ITbMJST CREST

    1B8-52 -

    17501830 PC 174017501B8-54, 1B8-55, 1B8-56, 1B8-571B8-54 redox C(sp3)-H

    1B8-55 redox

    1B8-56 redox

    1B8-57 2,3--2,3--1,4-2,3--1,4-

    328 900 1000

    PC 8509002B8-01, 2B8-02, 2B8-03, 2B8-04,2B8-05, 2B8-06

    2B8-01

    2B8-02 3 H8-BINOL

    2B8-03 3--H8-BINOL

    2B8-04

    2B8-05 -

    2B8-06 -

    10101110 PC 100010102B8-08, 2B8-10, 2B8-11, 2B8-12,

    2B8-132B8-08* Development of Ecient Asymmetric [3+2] Cycloaddition ReactionsUsing Chiral Copper Amide CatalystsGrad. Sch. Sci., The Univ. of TokyoYOSHIMOTO, Susumu; YAMASHITA, Yasuhiro; KOBAYASHI, Shu

    2B8-10 - Schiffendo [3+2]

    2B8-11 /

    2B8-12 -

    2B8-13

    11201220 PC 111011202B8-15, 2B8-16, 2B8-17, 2B8-18,

    2B8-19, 2B8-202B8-15 2

    2B8-16 -

    2B8-17

    2B8-18

    2B8-19 HBr HBr

    2B8-20 Henry

    328 13301430

    PC 132013302B8-28, 2B8-29, 2B8-30, 2B8-31,2B8-32, 2B8-33

    2B8-28

    2B8-29

    2B8-30 Artocarpin

    2B8-31 Valerenic acid

    2B8-32

    2B8-33 (+)-Duocarmycin A

    14401540 PC 143014402B8-35, 2B8-36, 2B8-37, 2B8-38,

    2B8-39, 2B8-402B8-35 19 D3A

    2B8-36 ()

  • 44

    2B8-37

    2B8-38

    2B8-39 -

    2B8-40

    15501640 PC 154015502B8-42, 2B8-43, 2B8-44, 2B8-45,

    2B8-462B8-42

    2B8-43 O-Phosohinative Passerini/Pudovik : - one-pot

    2B8-44 1Savukynas Vaidas

    2B8-45 2

    2B8-46 (E)-

    16501730 PC 164016502B8-48, 2B8-49, 2B8-50, 2B8-512B8-48

    2B8-49 6 3-[7]

    2B8-50 16 3--5-[7]

    2B8-51

    329 900 1000

    PC 8509003B8-01, 3B8-02, 3B8-03, 3B8-04,3B8-05, 3B8-06

    3B8-01 - N-/

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    3B8-03

    3B8-04

    3B8-05 (II)

    3B8-06

    10101110 PC 100010103B8-08, 3B8-09, 3B8-10, 3B8-11,

    3B8-123B8-08 (I)

    3B8-09 ,---

    3B8-10 3--2-

    3B8-11 ,--- N-

    3B8-12* ,- - N-

    11201220 PC 111011203B8-15, 3B8-16, 3B8-17, 3B8-18,

    3B8-203B8-15 Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxylate

    3B8-16

    3B8-17 1,2-E-WPI-ITbMJST CREST

    3B8-18* WPI-ITbMJSTCREST

    3B8-20 -

    329 17001800

    PC 165017003B8-49, 3B8-50, 3B8-52, 3B8-53,3B8-54

    3B8-49 ---

    3B8-50*

    3B8-52 2-

    3B8-53 ,

    3B8-54 Enantioselective Organocatalyzed Synthesis of Cyclobutanes viaformal [2+2] CycloadditionISIR, Osaka Univ.ARTEAGA, Fernandoarteaga; TAKIZAWA, Shinobu; SASAI, Hiroaki

    B9 ESES035

    H

    327

    13001400 PC 125013001B9-25, 1B9-26, 1B9-27, 1B9-291B9-25 2,2,2--1-()

    1B9-26

    1B9-27*

    1B9-29* Ecient amide bond formation through a rapid and strong activationof carboxylic acid, and its application for a synthesis of feglymycinGrad.Sch. Sci., Eng., Tokyo TechMIFUNE, Yuto; FUSE, Shinichiro; TANAKA,Hiroshi; TAKAHASHI, Takashi

    14101510 PC 140014101B9-32, 1B9-34, 1B9-35, 1B9-36,

    1B9-371B9-32* Multi-step Flow Synthesis of Optical Active -Amino Acid Deriva-tivesGrad. Sch. Sci., The Univ. of TokyoTSUBOGO, Tetsu;KOBAYASHI, Shu

    1B9-34

    1B9-35

    1B9-36

    1B9-37 -

    15201620 PC 151015201B9-39, 1B9-40, 1B9-41, 1B9-43,

  • 45

    1B9-441B9-39

    1B9-40 2-LeonardoDegennaroRenzo Luisi

    1B9-41*

    1B9-43

    1B9-44 Hydrogenation of aromatic compounds using polysilane supportedrhodium/platinum nanoparticlesGrad. Sch. Sci., The Univ. of TokyoTAMMINANA, Ramana; YASUKAWA, Tomohiro; MIYAMURA,

    Hiroyuki; KOBAYASHI, Shu

    328 900 1000

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    2B9-01

    2B9-02

    2B9-03

    2B9-04 Al-Sc

    2B9-05* The Development of an Enzyme-Mimetic System with Catechol-Stabilized Naked Platinum Nanoclusters: Homogeneous Cooperative Catalysis

    for Aerobic Oxidation of Amines to IminesGrad. Sch. Sci., The Univ. ofTokyoYUAN, Hao; MIYAMURA, Hiroyuki; KOBAYASHI, Shu

    10101110 PC 100010102B9-08, 2B9-09, 2B9-10, 2B9-11,

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    2B9-11

    2B9-12 1,3,5-[(4-)]

    2B9-13

    11201200 PC 111011202B9-15, 2B9-17, 2B9-182B9-15* Development of asymmetric synthesis catalyzed by biomass supportedchiral rhodium nanoparticles and study of structureGrad. Sch. Sci., TheUniv. of TokyoYASUKAWA, Tomohiro; MIYAMURA, Hiroyuki;KOBAYASHI, Shu

    2B9-17 Rh-

    2B9-18 1,4-

    329 900 1000

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    3B9-02

    3B9-03*

    3B9-05*

    10101110 PC 100010103B9-08, 3B9-10, 3B9-11, 3B9-12,

    3B9-133B9-08* The Eects of Amide Addition and Size of Nanoparticles in AerobicOxidation Reactions Catalyzed by Polymer Incarcerated Gold Nanoparticles

    Grad. Sch. Sci., The Univ. of TokyoMIN, Hyemin; SOULE, Jean-Francois; MIYAMURA, Hiroyuki; KOBAYASHI, Shu

    3B9-10 N-Alkylation of primary amides via hydrogen autotransfer facilitatedby metal nanoparticlesGrad. Sch. Sci., The Univ. of TokyoCHOO, ChongYu Gerald; MIYAMURA, Hiroyuki; KOBAYASHI, Shu

    3B9-11 Aerobic oxidative aromatization catalyzed by polymer incarceratedgold nanoclusterGrad. Sch. Sci., The Univ. of TokyoMIYAMURA,Hiroyuki; KOBAYASHI, Shu

    3B9-12

    3B9-13

    11201200 PC 111011203B9-15, 3B9-16, 3B9-17, 3B9-183B9-15 -

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    3B9-17 -DECHARIN Santida

    3B9-18

    C1 1 121

    327

    Fe

    900 1000 PC 8509001C1-01, 1C1-02, 1C1-03, 1C1-04,

    1C1-05, 1C1-061C1-01 -diketiminate

    1C1-02

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    1C1-04

    1C1-05 L-proline

    1C1-06 (III)

    Rh

    10101110 PC 100010101C1-08, 1C1-09, 1C1-10, 1C1-121C1-08 JSTACT-C

    1C1-09 Structures and Properties of Dinuclear Rhodium(I) Complexes withFormamidinato Bridging LigandsFac. Sci. Eng., Shimane Univ.; Sch. Sci.Tech., Kwansei Gakuin Univ.IDE, Yuki; IKEUE, Takahisa; INOUE,Ryoko; YOSHIOKA, Daisuke; MIKURIYA, Masahiro; HANDA, Makoto

    1C1-10* CO

    1C1-12*

  • 46

    Cr

    11201200 PC 111011201C1-15, 1C1-17, 1C1-181C1-15* 2ALCA, JSTLIU ShuoBOUGHERCurtHICKS ScottABU-OMAR Mahdi M.

    1C1-17 (V)-

    1C1-18 (V)

    328

    Co,Rh,Ir

    900 1010 PC 8509002C1-01, 2C1-02, 2C1-04, 2C1-05,

    2C1-06, 2C1-072C1-01 B12

    2C1-02* BadieiYosraMUCKERMAN James T.

    2C1-04 C1 Rh

    2C1-05 C-H

    2C1-06

    2C1-07 NCC

    10201130 PC 101010202C1-09, 2C1-10, 2C1-11, 2C1-12,

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    2C1-10 HCl

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    2C1-12 SiNN

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    2C1-14 2

    2C1-15

    328

    Co,Rh,Ir

    14301530 PC 142014302C1-34, 2C1-35, 2C1-36, 2C1-37,

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    2C1-35 Application of Bis(cyclometalated)iridium Complexes toward AlcoholOxidation and One-pot Dehydrogenative Silylation of Benzyl Alcohol

    DerivativesSch. Eng. Sci., Osaka Univ.CHOI, Gyeongshin; TSURUGI,Hayato; MASHIMA, Kazushi

    2C1-36 C-F

    2C1-37 C-N

    2C1-38 Ir-Vaska

    2C1-39 8 9 N-H

    15401640 PC 153015402C1-41, 2C1-42, 2C1-43, 2C1-44,

    2C1-462C1-41 2C1-42 Cp*Rh(III) Cp*Ir(III) 1,4-

    2C1-43 Ir(III)

    2C1-44* Cp*Ir(III)

    Ni,Pd,Pt

    2C1-46

    16501740 PC 164016502C1-48, 2C1-50, 2C1-51, 2C1-522C1-48*

    2C1-50 Pd

    2C1-51 Pd

    2C1-52

    329 900 1000

    PC 8509003C1-01, 3C1-02, 3C1-03, 3C1-