Wittig Reaction of 3-acyl-4-hydroxy-2(1H)-Quinolones. A New Route to Preparation of 3-alkyl/arylfuro[3,2-c] Quinolin-4(5H)-Ones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26520%2F00%3A63400009" target="_blank" >RIV/00216305:26520/00:63400009 - 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. A New Route to Preparation of 3-alkyl/arylfuro[3,2-c] Quinolin-4(5H)-Ones
Original language description
3-Acyl-4-hydroxy-2(1H)quinolines react with Wittig reagent to give 4-alkyl/aryl-pyrano[3,2-c]quinoline-2,5(6H)diones which more converted to furo[3,2-c] quinolin-4(5H)ones by bromination and following hydrolysis and decarboxylation.
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
2000
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Article name in the collection
8th Blue Danube Symposium on Heterocyclic Chemistry
ISBN
—
ISSN
—
e-ISSN
—
Number of pages
1
Pages from-to
—
Publisher name
Slovenian Chemical Society
Place of publication
University of Ljubljana
Event location
—
Event date
—
Type of event by nationality
—
UT code for WoS article
—