Generation of functional diversity via nitroaldol condensations of alpha-aminoacid aldehydes - A new and stereocontrolled route to acyclic 1,3-diamino-2-alcohols

被引:51
作者
Hanessian, S
Devasthale, PV
机构
[1] Department of Chemistry, Université de Montréal, Montréal, Qué. H3C 3J7, P.O.Box 6128, Station Centre-ville
关键词
D O I
10.1016/0040-4039(95)02359-3
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Condensations of N,N-dibenzyl alpha-amino aldehydes with nitroalkanes mediated by tetrabutylammonium fluoride proceed in excellent yields and selectivities. This affords rapid and stereoselective access to acyclic molecules containing differentiated nitrogen-containing functionality as well as diverse end groups.
引用
收藏
页码:987 / 990
页数:4
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