cheminform abstract: enantioselective ring-opening reaction of epoxides with meoh catalyzed by...

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ChemInform 2012, 43, issue 41 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Araliphatic ethers Q 0290 DOI: 10.1002/chin.201241067 Enantioselective Ring-Opening Reaction of Epoxides with MeOH Catalyzed by Homochiral Metal—Organic Framework. — Metal-organic frameworks, obtained from BDA, Cu(NO3)2 and Ph-NMe2, are applied as Lewis acid catalysts in the title reaction. — (TANAKA*, K.; OTANI, K.-I.; MURASE, T.; NISHIHOTE, S.; URBANCZYK-LIPKOWSKA, Z.; Bull. Chem. Soc. Jpn. 85 (2012) 6, 709-714, http://dx.doi.org/10.1246/bcsj.20110392 ; Dep. Chem. Mater. Eng., Fac. Chem., Mater. Bioeng., Kansai Univ., Suita, Osaka 564, Japan; Eng.) — M. Paetzel 41- 067

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Page 1: ChemInform Abstract: Enantioselective Ring-Opening Reaction of Epoxides with MeOH Catalyzed by Homochiral Metal—Organic Framework

Araliphatic ethersQ 0290 DOI: 10.1002/chin.201241067

Enantioselective Ring-Opening Reaction of Epoxides with MeOH Catalyzed by Homochiral Metal—Organic Framework. — Metal-organic frameworks, obtained from BDA, Cu(NO3)2 and Ph-NMe2, are applied as Lewis acid catalysts in the title reaction. — (TANAKA*, K.; OTANI, K.-I.; MURASE, T.; NISHIHOTE, S.; URBANCZYK-LIPKOWSKA, Z.; Bull. Chem. Soc. Jpn. 85 (2012) 6, 709-714, http://dx.doi.org/10.1246/bcsj.20110392 ; Dep. Chem. Mater. Eng., Fac. Chem., Mater. Bioeng., Kansai Univ., Suita, Osaka 564, Japan; Eng.) — M. Paetzel

41- 067

ChemInform 2012, 43, issue 41 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

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