Synthesis and Ring Transformation of Substituted S-(1-Phenylpyrrolidine-2-ones-3-yl)isothiouronium Salts to Substituted 2-Imino-5-[2-(Phenylamino)ethyl]-thiazolidine-4-ones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F02%3A00000185" target="_blank" >RIV/00216275:25310/02:00000185 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Synthesis and Ring Transformation of Substituted S-(1-Phenylpyrrolidine-2-ones-3-yl)isothiouronium Salts to Substituted 2-Imino-5-[2-(Phenylamino)ethyl]-thiazolidine-4-ones
Original language description
Substituted S-(1-phenylpyrrolidin-2-on-3-yl)isothiuronium salts in weakly basic media undergo intramolecular transformation reaction in which the gama-lactam cycle is split and a thiazolidine cycle is formed. A series of six substituted 2-imino-5-[2-(phenylamino)ethyl]thiazolidin-4-ones have been prepared by this reaction.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2002
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Heterocyclic Chemistry
ISSN
0022-152X
e-ISSN
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Volume of the periodical
39
Issue of the periodical within the volume
prosinec
Country of publishing house
US - UNITED STATES
Number of pages
3
Pages from-to
1105-1107
UT code for WoS article
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EID of the result in the Scopus database
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