Thiamine Derivatives of Disulfide Type. XV. The Ring Opening-closing Reactions of 4-Methylthiazolium Salts
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, University of Tokyo
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/21/4/21_4_858/_pdf
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Geometry and energy of amidoenethiolate conformers formed by ring-opening of several thiazolium ions in base: a theoretical study using density functional theory;Arkivoc;2001-11-25
2. Kinetics and mechanism of the reversible ring-opening of thiamine and related thiazolium ions in aqueous solution;Journal of the Chemical Society, Perkin Transactions 2;1997
3. Hydrolysis of Thiamin: Evidence for Rate-Limiting Breakdown of the Tricyclic Dihydrothiachromine Intermediate in Neutral Aqueous Solution;Bioorganic Chemistry;1993-06
4. Mechanism of hydrolysis of a thiazolium ion: General acid-base catalysis of the breakdown of the tetrahedral addition intermediate;Bioorganic Chemistry;1992-12
5. Reversible hydrolysis of the 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium cation in aqueous solution;Journal of the Chemical Society, Perkin Transactions 2;1992
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