Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines

The triazine ring bearing a trichloromethyl group was annelated to various aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of trichloroacetamidines in the reaction of aminoazoles with trichloroacetonitrile followed by the triazine ring clos...

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Bibliographic Details
Main Authors: Kalinin, D., Kalinina, S., Dolzhenko, Anton
Format: Journal Article
Published: The Japan Institute of Heterocyclic Chemistry 2012
Online Access:http://hdl.handle.net/20.500.11937/14859
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author Kalinin, D.
Kalinina, S.
Dolzhenko, Anton
author_facet Kalinin, D.
Kalinina, S.
Dolzhenko, Anton
author_sort Kalinin, D.
building Curtin Institutional Repository
collection Online Access
description The triazine ring bearing a trichloromethyl group was annelated to various aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of trichloroacetamidines in the reaction of aminoazoles with trichloroacetonitrile followed by the triazine ring closure with triethyl orthoformate affording therefore the titled compounds.
first_indexed 2025-11-14T07:09:47Z
format Journal Article
id curtin-20.500.11937-14859
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T07:09:47Z
publishDate 2012
publisher The Japan Institute of Heterocyclic Chemistry
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-148592017-09-13T16:04:39Z Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines Kalinin, D. Kalinina, S. Dolzhenko, Anton The triazine ring bearing a trichloromethyl group was annelated to various aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of trichloroacetamidines in the reaction of aminoazoles with trichloroacetonitrile followed by the triazine ring closure with triethyl orthoformate affording therefore the titled compounds. 2012 Journal Article http://hdl.handle.net/20.500.11937/14859 10.3987/COM-12-12542 The Japan Institute of Heterocyclic Chemistry restricted
spellingShingle Kalinin, D.
Kalinina, S.
Dolzhenko, Anton
Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title_full Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title_fullStr Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title_full_unstemmed Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title_short Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
title_sort synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
url http://hdl.handle.net/20.500.11937/14859