Synthesis of a new enantiomerically pure constrained homoserine.

被引：32

作者：

Avenoza, A

Cativiela, C

FernandezRecio, MA

Peregrina, JM

机构：

[1] UNIV ZARAGOZA,CSIC,INST CIENCIA MAT ARAGON,DEPT ORGAN CHEM,E-50009 ZARAGOZA,SPAIN

[2] UNIV LA RIOJA,DEPT CHEM ORGAN CHEM,SECC CIENCIAS,E-26001 LOGRONO,SPAIN

来源：

TETRAHEDRON-ASYMMETRY | 1996年 / 7卷 / 03期

关键词：

D O I：

10.1016/0957-4166(96)00067-5

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The use of the Diels-Alder reaction between 1,3-butadiene and chiral 2-acetamidoacrylates as the key step followed by stereocontrolled transformations allows the synthesis of (1S, 3R)-1-amino-3-hydroxycyclohexanecarboxylic acid, a new type of constrained homoserine, with an excellent overall yield. (C) 1996 Elsevier Science Ltd

引用

页码：721 / 728

页数：8

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