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Preparation of 2-Alkyl/Arylfuro[3,2-c]quinoline-4(5H)-ones via Molecular Rearrangement of 4-Alkyl/Aryl-3-bromopyrano[3,2-c]quinoline-2,5(2H,6H)-diones

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F01%3A63500211" target="_blank" >RIV/70883521:28110/01:63500211 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Preparation of 2-Alkyl/Arylfuro[3,2-c]quinoline-4(5H)-ones via Molecular Rearrangement of 4-Alkyl/Aryl-3-bromopyrano[3,2-c]quinoline-2,5(2H,6H)-diones

  • Original language description

    4-Alkyl/Arylpyrano[3,2-c]quinoline-2,5(2H,6H)-diones were prepared by the reaction of 3-acyl-4-hydroxy-2(1H)quinolones with (triphenylphosphoranylidene)acetate. By their bromination,4-alkyl/aryl-2-bromopyrano[3,2-c]quinoline-2,5(2H,6H) -diones arise, which rearrange during alkaline hydrolysis to give 2-alkyl/arylfuro[3,2-c] quinoline-4(5H)-ones. The reaction mechanism of the molecular rearrangement is discussed.

  • 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

    2001

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    18th International Congress of Heterocyclic Chemistry

  • ISBN

  • ISSN

  • e-ISSN

  • Number of pages

    1

  • Pages from-to

  • Publisher name

    International Society of Heterocyclic Chemistry

  • Place of publication

    Yokohama

  • Event location

    Yokohama

  • Event date

    Aug 24, 2001

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article