The chemistry of carbamates
Carbamic acid, H2NCOOH, the half amide of carbonic acid, does not exist as the free acid. Only some heterocyclic carbamic acids form relatively stable compounds. In contrast to this, carbamates including derivatives resulting from replacement of hydrogen atoms at the nitrogen atom by organic radical...
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ftunivpardubice:oai:dk.upce.cz:10195/32623 2023-07-16T03:57:57+02:00 The chemistry of carbamates Mindl, Jaromír Čegan, Alexandr 2000 p. 129-164 application/pdf http://hdl.handle.net/10195/32623 eng eng Univerzita Pardubice Scientific papers of the University of Pardubice. Series A, Faculty of Chemical technology. 5 (1999) Univerzitní knihovna (studovna) 1211-5541 http://hdl.handle.net/10195/32623 47333 open access karbamáty struktura analytické metody deriváty reakce organická chemie article 2000 ftunivpardubice 2023-06-27T18:24:31Z Carbamic acid, H2NCOOH, the half amide of carbonic acid, does not exist as the free acid. Only some heterocyclic carbamic acids form relatively stable compounds. In contrast to this, carbamates including derivatives resulting from replacement of hydrogen atoms at the nitrogen atom by organic radicals form quite stable compounds. The chemistry of carbamates was first reviewed by Adams and Baron [1] in 1965. The carbamate function as considered in this review is based on the trivalent group -O-CO-Nˇ. On attaching various radicals to three free valences of this group, on can obtain many classes of compounds, including the cyclic carbamates as 1,3-oxyzol-2-ones or 1,3-oxazin-2-ones. This article is based on the author's original papers and on some other recently published ones. Article in Journal/Newspaper Carbonic acid Digitální knihovna Univerzity Pardubice |
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Open Polar |
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Digitální knihovna Univerzity Pardubice |
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ftunivpardubice |
language |
English |
topic |
karbamáty struktura analytické metody deriváty reakce organická chemie |
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karbamáty struktura analytické metody deriváty reakce organická chemie Mindl, Jaromír Čegan, Alexandr The chemistry of carbamates |
topic_facet |
karbamáty struktura analytické metody deriváty reakce organická chemie |
description |
Carbamic acid, H2NCOOH, the half amide of carbonic acid, does not exist as the free acid. Only some heterocyclic carbamic acids form relatively stable compounds. In contrast to this, carbamates including derivatives resulting from replacement of hydrogen atoms at the nitrogen atom by organic radicals form quite stable compounds. The chemistry of carbamates was first reviewed by Adams and Baron [1] in 1965. The carbamate function as considered in this review is based on the trivalent group -O-CO-Nˇ. On attaching various radicals to three free valences of this group, on can obtain many classes of compounds, including the cyclic carbamates as 1,3-oxyzol-2-ones or 1,3-oxazin-2-ones. This article is based on the author's original papers and on some other recently published ones. |
format |
Article in Journal/Newspaper |
author |
Mindl, Jaromír Čegan, Alexandr |
author_facet |
Mindl, Jaromír Čegan, Alexandr |
author_sort |
Mindl, Jaromír |
title |
The chemistry of carbamates |
title_short |
The chemistry of carbamates |
title_full |
The chemistry of carbamates |
title_fullStr |
The chemistry of carbamates |
title_full_unstemmed |
The chemistry of carbamates |
title_sort |
chemistry of carbamates |
publisher |
Univerzita Pardubice |
publishDate |
2000 |
url |
http://hdl.handle.net/10195/32623 |
genre |
Carbonic acid |
genre_facet |
Carbonic acid |
op_relation |
Scientific papers of the University of Pardubice. Series A, Faculty of Chemical technology. 5 (1999) Univerzitní knihovna (studovna) 1211-5541 http://hdl.handle.net/10195/32623 47333 |
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open access |
_version_ |
1771544874157342720 |