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Gold-catalyzed stereoselective synthesis of 9-oxabicyclo[3.3.1]nona-4,7- dienes from diverse 1-oxo-4-oxy-5-ynes: A viable formal [4 + 2] cycloaddition on an s-trans-heterodiene framework
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Gold-catalyzed stereoselective synthesis of 9-oxabicyclo[3.3.1]nona-4,7- dienes from diverse 1-oxo-4-oxy-5-ynes: A viable formal [4 + 2] cycloaddition on an s-trans-heterodiene framework

Tse-Min Teng, Arindam Das, Deepak B. Huple and Rai-Shung Liu
Journal of the American Chemical Society, Vol.132(36), pp.12565-12567
15/09/2010

Abstract

We report a highly stereoselective Au-catalyzed synthesis of 9-oxabicyclo[3.3.1]nona-4,7-dienes from diverse 1-oxo-4-oxy-5-ynes. Formation of these highly strained anti-Bredt oxacycles implies the workability of an unprecedented 1,4-dipole of s-trans-methylene(vinyl)oxonium. This work reveals the feasibility of a formal [4 + 2] cycloaddition on an s-trans-heterodiene framework. © 2010 American Chemical Society.

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