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
—