Formation of 3-[amino(aryl)-methylidene]-1,3-dihydro-2 H -indol-2-ones involving ring transformation of 2-aryl-5-(2-aminophenyl)-4-hydroxy-1,3-thiazoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Synthesis and ring transformation of substitutedS-(1-phenylpyrrolidine-2-ones-3-yl)isothiuronium salts to substituted 2-imino-5-[2-(phenylamino)ethyl]thiazolidin-4-ones
2. Kinetics and mechanism of ring transformation of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide to 2-methylimino-5-[2-(4-methoxyphenylamino)ethyl]thiazolidin-4-one
3. Influence of substitution on kinetics and mechanism of ring transformation of substituted S-[1-phenylpyrrolidin-2-on-3-yl]isothiuronium salts
4. Efficient synthesis of 5-(2-hydroxyethyl)-2-phenylimino- 1,3-thiazolidin-4-ones and 5-(2-hydroxyethyl)-2-phenylamino-4,5-dihydro-1,3-thiazol-4-ones
5. Kinetic Evidence for the Coexistence of Zwitterionic (T±), Neutral (T0) and Anionic (T−) Intermediates during Rearrangement of S-(2-Oxotetrahydrofuran-3-yl)-N-(4-methoxyphenyl)isothiuronium Bromide to 5-(2-Hydroxyethyl)-2-(4-methoxyphenylimino)-1,3-thiazolidin-4-one
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