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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

  • DOI - Digital Object Identifier

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

  • 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

    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

  • 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

  • EID of the result in the Scopus database