A new approach to the stereoselective synthesis of conveniently protected alpha-allyl substituted amino acids; Chiral key compounds in the synthesis of constrained peptide isostere constituents

被引：30

作者：

Badorrey, R ^{[1
]}

Cativiela, C ^{[1
]}

DiazDeVillegas, MD ^{[1
]}

Galvez, JA ^{[1
]}

Lapena, Y ^{[1
]}

机构：

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

来源：

TETRAHEDRON-ASYMMETRY | 1997年 / 8卷 / 02期

关键词：

D O I：

10.1016/S0957-4166(96)00516-2

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Enantiomerically pure alpha-allyl-N-Boc-aminoamides were prepared by Curtius rearrangement of alpha,alpha-dialkyl chiral 2-cyanoesters obtained by the diastereoselective allylation of chiral 2-cyanoesters according to a modification of our previously described procedure. (C) 1997 Elsevier Science Ltd.

引用

页码：311 / 317

页数：7

共 31 条

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