3-Amino-2,4(1H,3H)-Quinolinediones and some Possibilities of their Synthetic Utilization

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F02%3A63500549" target="_blank" >RIV/70883521:28110/02:63500549 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

3-Amino-2,4(1H,3H)-Quinolinediones and some Possibilities of their Synthetic Utilization

Original language description

Primary 3-aminoquinoline-2,4-diones were prepared by the reaction of corresponding 3-chloro derivatives with ammonium chloride and potassium carbonate in dimethylformamide. Their secondary analogues were prepared by the reaction of 3-chloro derivatives with excess of aliphatic primary amines. Both types of 3-amino derivatives rect with Wittig reagent to give ethyl (3-amino-2-oxo-2,3-dihydro-1H-quinolin-4E-yliden)acetates and 3,3a-dihydro-5H-pyrrolo[2,3-c]quinoline-2,4-diones.

Czech name

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Czech description

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Type

D - Article in proceedings

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2002

Confidentiality

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

Article name in the collection

8th IBN SINA - International Conference on Pure and Applied Heterocyclic Chemistry - book of abstracts

ISBN

nemá

ISSN

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e-ISSN

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Number of pages

1

Pages from-to

355

Publisher name

Chemistry Department Faculty of Science, Assiut University

Place of publication

Assiut

Event location

Luxor, Egypt

Event date

Feb 16, 2002

Type of event by nationality

EUR - Evropská akce

UT code for WoS article

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