| ČMELÍK, Richard, Jaromír MAREK a Pavel PAZDERA. A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures. Heterocyclic Communications. London: Freund Publishing House, roč. 2002, č. 1, s. 55-60. ISSN 0793-0283. 2002. |
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@article{403456,
author = {Čmelík, Richard and Marek, Jaromír and Pazdera, Pavel},
article_location = {London},
article_number = {1},
keywords = {regioselectivity; 1;2-dithiole; alkylation; acylation; 1;2-dithiolium; hydrogen bonding; X-ray structural analysis},
language = {eng},
issn = {0793-0283},
journal = {Heterocyclic Communications},
title = {A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures},
volume = {2002},
year = {2002}
}
TY - JOUR
ID - 403456
AU - Čmelík, Richard - Marek, Jaromír - Pazdera, Pavel
PY - 2002
TI - A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures
JF - Heterocyclic Communications
VL - 2002
IS - 1
SP - 55
EP - 55
PB - Freund Publishing House
SN - 07930283
KW - regioselectivity
KW - 1;2-dithiole
KW - alkylation
KW - acylation
KW - 1;2-dithiolium
KW - hydrogen bonding
KW - X-ray structural analysis
N2 - 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.
ER -
ČMELÍK, Richard, Jaromír MAREK a Pavel PAZDERA. A regioselectivity of electrophilic attacks to 5-amino-3-thioxo-3H-1,2-dithiole-4-carboxylic acid functional derivatives. An elucidation of product structures. \textit{Heterocyclic Communications}. London: Freund Publishing House, roč.~2002, č.~1, s.~55-60. ISSN~0793-0283. 2002.
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