STEREOSELECTIVE ALKYLATION OF CHIRAL GLYCINE ENOLATE SYNTHONS - THE ENANTIOSELECTIVE SYNTHESIS OF ALPHA-AMINO-ACID DERIVATIVES

被引：42

作者：

DELLARIA, JF ^{[1
]}

SANTARSIERO, BD ^{[1
]}

机构：

[1] HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 47期

关键词：

D O I：

10.1016/S0040-4039(00)82269-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6079 / 6082

页数：4

共 17 条

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[5] STERICALLY CONTROLLED SYNTHESIS OF OPTICALLY ACTIVE ORGANIC-COMPOUNDS .23. ASYMMETRIC SYNTHESIS OF ALANINE BY ALKYLATION OF OPTICALLY-ACTIVE N-ALKYL-N-FORMYLAMINOACETONITRILES
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[6] ASYMMETRIC-SYNTHESIS OF ALPHA-AMINO-ACIDS BY ALKYLATION OF A GLYCINE AMIDE DERIVATIVE BEARING CHIRAL 2,5-DISUBSTITUTED PYRROLIDINE AS AN AMINE COMPONENT
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[7] ALLYLIC STRAIN IN 6-MEMBERED RINGS
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[8] KOLB M, 1979, TETRAHEDRON LETT, V32, P2999
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