SYNTHESIS OF NEW F-ALKYLATED AMINO-ACIDS DERIVED FROM LYSINE, ARGININE AND CYSTEINE

被引：6

作者：

HADDACH, M

PASTOR, R

RIESS, JG

机构：

[1] Laboratoire de Chimie Moléculaire, Associé au CNRS, Université de Nice-Sophia Antipolis

来源：

JOURNAL OF FLUORINE CHEMISTRY | 1991年 / 51卷 / 02期

关键词：

D O I：

10.1016/S0022-1139(00)80290-0

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Ethyl-2-F-alcynoates are good substrates for Michael additions. Such additions allowed the preparation of three new families of F-alkylated aminoacids derived from lysine, arginine and cysteine. However, their transformation into betaines has proved more difficult than in the hydrocarbon series.

引用

页码：197 / 205

页数：9

共 10 条

[1]

BLAIGNON C, 1988, 2ND P WORLD SURF C P, V2, P137

[2]

CARTER HE, 1940, J BIOL CHEM, P109

[3] SYNTHESIS AND REACTIVITY OF ETHYL 3-PERFLUOROALKYL-3-ALKYLTHIOPROPENOATES - PERFLUOROALKYLATED THIOPHENES AND BETA-THIOXOESTERS [J].