Gold Catalysis: Switching the Pathway of the Furan??Yne Cyclization

…, M Rudolph, J Huck, W Frey, JW Bats…

Index: Hashmi, A. Stephen K.; Rudolph, Matthias; Huck, Juergen; Frey, Wolfgang; Bats, Jan W.; Hamzic, Melissa Angewandte Chemie - International Edition, 2009 , vol. 48, # 32 p. 5848 - 5852

Full Text: HTML

Citation Number: 84

Abstract

The use of gold compounds as homogeneous catalysts for the conversion of many organic substrates is one of the fastest growing areas in organic chemistry today.[1] Among these transformations, the cyclization of ene–ynes is playing a major role.[2] We developed the gold-catalyzed synthesis of highly substituted phenols, starting from furan–alkyne systems. In this case, as in most of the common ene–yne systems, the first step of the reaction is ...

Related Articles:

A convenient and general preparation of N-sulfonylimines

[Boger, Dale L.; Corbett, Wendy L. Journal of Organic Chemistry, 1992 , vol. 57, # 17 p. 4777 - 4780]

Triarylmethyl chlorides as novel, efficient, and mild organic catalysts for the synthesis of N-sulfonyl imines under neutral conditions

[Patel, Rajesh; Srivastava, Vishnu P.; Yadav, La Dhar S. Advanced Synthesis and Catalysis, 2010 , vol. 352, # 10 p. 1610 - 1614]

More Articles...