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

dc.contributor.author	Kalinin, D.
dc.contributor.author	Kalinina, S.
dc.contributor.author	Dolzhenko, Anton
dc.date.accessioned	2017-01-30T11:46:29Z
dc.date.available	2017-01-30T11:46:29Z
dc.date.created	2012-11-01T20:00:25Z
dc.date.issued	2012
dc.identifier.citation	Kalinin, Dmitrii and Kalinina, Svetlana and Dolzhenko, Anton. 2012. Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines. Heterocycles. 85 (10): pp. 2515-2522.
dc.identifier.uri	http://hdl.handle.net/20.500.11937/14859
dc.identifier.doi	10.3987/COM-12-12542
dc.description.abstract	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.
dc.publisher	The Japan Institute of Heterocyclic Chemistry
dc.title	Synthesis of novel trichloromethyl substituted azolo[1,3,5]triazines
dc.type	Journal Article
dcterms.source.volume	85
dcterms.source.number	10
dcterms.source.startPage	2515
dcterms.source.endPage	2522
dcterms.source.issn	1881-0942
dcterms.source.title	Heterocycles
curtin.department
curtin.accessStatus	Fulltext not available