Chelation-controlled ester-derived titanium enolate aldol reaction: diastereoselective syn-aldols with mono- and bidentate aldehydes
摘要:
A chelation-controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of (S)-valinolderived ester with a variety of aldehydes proceeded with high syn-diastercoselectivities (up to 99:1) and isolated yields (94%). (C) 2002 Elsevier Science Ltd. All rights reserved.
Ester derived titanium enolate aldol reaction: chelation controlled diastereoselective synthesis of syn -aldols
作者:Arun K Ghosh、Jae-Hun Kim
DOI:10.1016/s0040-4039(00)02227-9
日期:2001.2
A chelation controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of commercially available l-phenylalaninol derived esters with a variety of bidentate oxyaldehydes proceeded with excellent syn-diastereoselectivities and isolated yields.