Ring Transformation of the S-(2-Oxo-2,3-dihydro-1-benzofuran-3-yl)isothiuronium Bromides to 5-(2-Hydroxyphenyl)-2-imino-1,3-thiazolidin-4-ones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F14%3A39897720" target="_blank" >RIV/00216275:25310/14:39897720 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.3987/COM-14-12967" target="_blank" >http://dx.doi.org/10.3987/COM-14-12967</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3987/COM-14-12967" target="_blank" >10.3987/COM-14-12967</a>
Alternative languages
Result language
angličtina
Original language name
Ring Transformation of the S-(2-Oxo-2,3-dihydro-1-benzofuran-3-yl)isothiuronium Bromides to 5-(2-Hydroxyphenyl)-2-imino-1,3-thiazolidin-4-ones
Original language description
Synthesis of thirteen substituted 5-(2-hydroxyethyl)-2-phenylimino-1,3-thiazolidin-4-ones is described starting from easily available and stable S-(2-oxo-2,3-dihydro-1-benzofuran-3-yl)isothiuronium bromides. The transformation proceeds under mild conditions, is very simple to perform, and is applicable to a wide range of substituents on isothiuronium moiety. Some 1,3-thiazolidin-4-ones show dynamic NMR behavior in solution because of prototropy tautomerism and E-/Z-stereoisomerism. Thermochromic behavior was observed for all synthesized compound.
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
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2014
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Heterocycles
ISSN
0385-5414
e-ISSN
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Volume of the periodical
89
Issue of the periodical within the volume
5
Country of publishing house
JP - JAPAN
Number of pages
12
Pages from-to
1183-1194
UT code for WoS article
000336872600004
EID of the result in the Scopus database
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