New quinone-amino acid conjugates linked via a vinylic spacer

被引：12

作者：

Alnabari, M ^{[1
]}

Bittner, S ^{[1
]}

机构：

[1] Ben Gurion Univ Negev, Dept Chem, IL-84105 Beer Sheva, Israel

来源：

AMINO ACIDS | 2001年 / 20卷 / 04期

关键词：

amino acids; quinones; chloranil; 2,3-dichloro-1,4-naphthoquinone; transamination;

D O I：

10.1007/s007260170034

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Chloranil and 2,3-dichloro-1,4-naphthoquinone have been linked to different natural and unnatural amino acids via a vinylic spacer. Two routes were developed for the facile preparation of these novel modified amino acids: the direct method, which can only be applied to secondary amines, and the indirect method (transamination reaction), which can be applied to any amino acid or ester.

引用

页码：381 / 387

页数：7

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