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...
| Main Authors: | , , |
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| Format: | Journal Article |
| Published: |
The Japan Institute of Heterocyclic Chemistry
2012
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| Online Access: | http://hdl.handle.net/20.500.11937/14859 |
| _version_ | 1848748736148144128 |
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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 |