cheminform abstract: palladium-catalyzed carbonylative cycloisomerization of...

ChemInform 2010, 41, issue 13 © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Furan derivatives R 0060 DOI: 10.1002/chin.201013102 Palladium-Catalyzed Carbonylative Cycloisomerization of γ-Propynyl-1,3-dike- tones: A Concise Route to Polysubstituted Furans. — Di- and trisubstituted furans as well as benzofuran derivatives can be prepared efficiently. The nature of C-1 substi- tuent (R) and linker length between carbonyl and alkyne group has strong influence on the success. — (LI, Y.; YU*, Z.; J. Org. Chem. 74 (2009) 22, 8904-8907; Dalian Inst. Chem. Phys., Chin. Acad. Sci., Dalian 116023, Peop. Rep. China; Eng.) — Jannicke 13- 102

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Page 1: ChemInform Abstract: Palladium-Catalyzed Carbonylative Cycloisomerization of γ-Propynyl-1,3-diketones: A Concise Route to Polysubstituted Furans

www.cheminform.wiley-vch.de

Furan derivativesR 0060 DOI: 10.1002/chin.201013102

Palladium-Catalyzed Carbonylative Cycloisomerization of γ-Propynyl-1,3-dike-tones: A Concise Route to Polysubstituted Furans. — Di- and trisubstituted furans as well as benzofuran derivatives can be prepared efficiently. The nature of C-1 substi-tuent (R) and linker length between carbonyl and alkyne group has strong influence on the success. — (LI, Y.; YU*, Z.; J. Org. Chem. 74 (2009) 22, 8904-8907; Dalian Inst. Chem. Phys., Chin. Acad. Sci., Dalian 116023, Peop. Rep. China; Eng.) — Jannicke

13- 102

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