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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

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • 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

  • 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