960化工网
A stereoselective synthesis of anti-γ,δ-alkynyl- and -alkenyl-β-hydroxy-α-amino esters from tin(ii) enolates of glycinate†
Jonathan J. Gridley,Michael P. Coogan,David W. Knight,K. M. Abdul Malik,Christopher M. Sharland,Jirada Singkhonrat,Siân Williams
Chemical Communications Pub Date : 09/17/2003 00:00:00 , DOI:10.1039/B306291K
Abstract

Condensations between the tin(II) enolate 11 of ethyl N-tosylglycinate and conjugated ynals 12 and ynones 14 are highly diastereoselective, in favour of the anti-isomers 13 and 15; similar reactions of enals and enones 17 show lower but still useful levels of anti-stereoselectivity.

Graphical abstract: A stereoselective synthesis of anti-γ,δ-alkynyl- and -alkenyl-β-hydroxy-α-amino esters from tin(ii) enolates of glycinate
平台客服
平台客服
平台在线客服