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Wittig Reaction of 3-Acyl-4-hydroxy-2(1H)-Quinolones

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F02%3A63500552" target="_blank" >RIV/70883521:28110/02:63500552 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Wittig Reaction of 3-Acyl-4-hydroxy-2(1H)-Quinolones

  • Original language description

    The Wittig reaction of title compounds with ethyl(triphenylphosphoranylidene)acetate afford 4-alkyl/arylpyrano[3,2-c] quinoline-2,5(6H)-diones. These compounds were brominated to their 3-bromo derivatives. The hydrolysis of bromoderivatives proceed witha molecular rearrangement and afford 2-alkyl/aryl-4-oxo-5H-furo[3,2-c]quinoline-3-carboxylic acids.

  • Czech name

  • Czech description

Classification

  • Type

    D - Article in proceedings

  • 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

  • Article name in the collection

    9th Blue Danube Symposium on Heterocyclic Chemistry - book of abstracts

  • ISBN

    80-227-1705-3

  • ISSN

  • e-ISSN

  • Number of pages

    1

  • Pages from-to

    138

  • Publisher name

    Publishing House of Slovak University of Technology

  • Place of publication

    Bratislava

  • Event location

    Tatranská Lomnica

  • Event date

    Jun 16, 2002

  • Type of event by nationality

    EUR - Evropská akce

  • UT code for WoS article