Study of some reactions of 5-nitroisatine accompanied with nucleophilic substitution of aminogroup

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F00%3A00000985" target="_blank" >RIV/61989592:15310/00:00000985 - 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

Study of some reactions of 5-nitroisatine accompanied with nucleophilic substitution of aminogroup

Original language description

Earlier work described the conversion of 5-nitroisatine thiosemicarbazone in solution of sodium bicarbonate to 5-(2-amino-5-nitrophenyl)-6-azauracil. We performed this reaction in solution of sodium hydroxide and 5-(2-hydroxy-5-nitrophenyl)-6-azauracil was isolated instead. Also reaction of 5-nitroisatine with thiosemicarbazide in solution of sodium hydroxide afforded the 5-(2-hydroxy-5-nitrophenyl)-6-azauracil.

Czech name

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Czech description

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Type

C - Chapter in a specialist book

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

2000

Confidentiality

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

Book/collection name

8th Blue Danube Symposium on Heterocyclic Chemistry

ISBN

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Number of pages of the result

198

Pages from-to

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Number of pages of the book

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Publisher name

University of Ljubljana

Place of publication

Ljubljana- Slovenia

UT code for WoS chapter

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