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Enantiocontrolled construction of tricyclic furan derivatives via an asymmetric Diels-Alder reaction
Journal article   Peer reviewed

Enantiocontrolled construction of tricyclic furan derivatives via an asymmetric Diels-Alder reaction

Chung-Cheng Pai and Rai-Shung Liu
Organic Letters, Vol.3(9), pp.1295-1297
03/05/2001

Abstract

(equation presented) The two enantiomers of trycyclic furan derivatives were prepared respectively from Diels-Alder reactions of oxycyclic dienes 3a and 3b, followed by degradation of the 2-(benzyloxy)ethyl group. Compounds 3a and 3b can be selectively synthesized by [3+2]-cycloaddition of vinylpropargyltungsten complex with (2S)-(benzyloxy)-propanal.

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