A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F02%3A00005700" target="_blank" >RIV/00216224:14310/02:00005700 - 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

A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures

Original language description

An acylation of 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives led to the formation of N-acyl compound via S-acyl intermediate. On the other hand, alkylation occurred only at the sulfur atom of thioxo group. Structure elucidation of both types of products was done by IR, 1H, 13C NMR and X-ray structural analysis.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/GA203%2F01%2F1333" target="_blank" >GA203/01/1333: Chalcogen organic compounds - synthesis, transformation and structure elucidation</a><br>

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

Name of the periodical

Heterocyclic Communications

ISSN

0793-0283

e-ISSN

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Volume of the periodical

2002

Issue of the periodical within the volume

1

Country of publishing house

GB - UNITED KINGDOM

Number of pages

6

Pages from-to

55

UT code for WoS article

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EID of the result in the Scopus database

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