Diversity-oriented synthesis of amino acids using chiral enolates

被引：5

作者：

Sen, Subhabrata ^{[1
]}

Kamma, Siva R. ^{[1
]}

Potti, Venkata R. ^{[1
]}

Murthy, Y. L. N. ^{[2
]}

Chaudhary, Avinash B. ^{[1
]}

机构：

[1] GVK Biosci, Hyderabad, Andhra Pradesh, India

[2] Andhra Univ, Dept Chem Food Drugs & Water, Coll Sci & Technol, Vishakhapatnam, India

来源：

TETRAHEDRON LETTERS | 2011年 / 52卷 / 43期

关键词：

Diversity oriented synthesis; alpha-Amino acid; beta-Amino acid; Mannich reaction; Pluripotent functional group; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; DERIVATIVES; CATALYSIS; CYANIDE;

D O I：

10.1016/j.tetlet.2011.08.052

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We report a facile diversity oriented synthesis of alpha- and beta-amino acids, by utilizing the pluripotent alpha-methylene group in a chiral bicyclic lactam as our key point of transformation. (C) 2011 Elsevier Ltd. All rights reserved.

引用

页码：5585 / 5588

页数：4

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