Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26520%2F00%3A63400007" target="_blank" >RIV/00216305:26520/00:63400007 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Synthesis of Novel 3-Acyloxy-1,3-dihydro-2H-indol-2-ones and Isomeric 4-Acyl-1,4-dihydro-3,1- benzoxazin-2-ones. Double Rearrangement of 3-Hydroxyquinoline-2,4(1H,3H)-diones
Original language description
Substituted 3-hydroxyquinoline-2,4(1H,3H)-diones 3 were transformed into 3-acyloxy-1,3-dihydro-2H indol-2-ones 4 and isomeric 4-acyl-1,4-dihydro-3,1-benzoaxazin-2-ones 5.The influence of the substituents and the reaction conditions on the course of the reaction was studied. In the proposed mechanism a double rearrangement takes place.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
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
Name of the periodical
Tetrahedron
ISSN
0040-4020
e-ISSN
—
Volume of the periodical
56
Issue of the periodical within the volume
March
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
—
UT code for WoS article
—
EID of the result in the Scopus database
—