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
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DOI - Digital Object Identifier
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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
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Czech description
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Classification
Type
D - Article in proceedings
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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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
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ISSN
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e-ISSN
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Number of pages
1
Pages from-to
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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
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