Dimerization of an intermediate during the sodium in liquid ammonia reduction ofl-thiazolidine-4-carboxylic acid
作者:
P. Blondeau,
C. Berse,
D. Gravel,
期刊:
Canadian Journal of Chemistry
(NRC Available online 1967)
卷期:
Volume 45,
issue 1
页码: 49-52
ISSN:0008-4042
年代: 1967
DOI:10.1139/v67-009
出版商: NRC Research Press
数据来源: NRC
摘要:
Reduction with sodium in liquid ammonia ofl-thiazolidine-4-carboxylic acid (II) leads, depending on the reaction procedure followed, toN-methyl-l-cysteine (I) or a mixture ofN-methyl-l-cysteine (I) (30%) and a dimer (50%), the structure of which is shown to be VI. Contrary to what has been expressed in the literature, the reaction of 1,2-dichloroethane with cysteine (III) at a pH of 8–10 does not lead to compound VI but to compound VIII.
点击下载:
PDF
(607KB)
返 回