A new synthesis of amino substituted azolo[1,3,5]triazines via reaction of N1,N1-dimethyl-N2-azolylformamidines with cyanamide
| dc.contributor.author | Kalinin, D. | |
| dc.contributor.author | Kalinina, S. | |
| dc.contributor.author | Dolzhenko, Anton | |
| dc.date.accessioned | 2017-01-30T10:52:42Z | |
| dc.date.available | 2017-01-30T10:52:42Z | |
| dc.date.created | 2014-02-26T20:00:30Z | |
| dc.date.issued | 2013 | |
| dc.identifier.citation | Kalinin, Dimitrii V. and Kalinina, Svetlana A. and Dolzhenko, Anton V. 2013. A new synthesis of amino substituted azolo[1,3,5]triazines via reaction of N1,N1-dimethyl-N2-azolylformamidines with cyanamide. Heterocycles. 87 (1): pp. 147-154. | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11937/6387 | |
| dc.identifier.doi | 10.3987/COM-12-12601 | |
| dc.description.abstract |
The amino substituted triazine ring was annelated to aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of azolylformamidines in the reaction of aminoazoles with N,N-dimethylformamide dimethyl acetal followed by the triazine ring closure with cyanamide affording therefore fused aminotriazines. | |
| dc.publisher | The Japan Institute of Heterocyclic Chemistry | |
| dc.subject | adenines | |
| dc.subject | cyanamide | |
| dc.subject | triazines | |
| dc.subject | benzimidazoles | |
| dc.subject | triazoles | |
| dc.subject | pyrazoles | |
| dc.title | A new synthesis of amino substituted azolo[1,3,5]triazines via reaction of N1,N1-dimethyl-N2-azolylformamidines with cyanamide | |
| dc.type | Journal Article | |
| dcterms.source.volume | 87 | |
| dcterms.source.number | 1 | |
| dcterms.source.startPage | 147 | |
| dcterms.source.endPage | 154 | |
| dcterms.source.issn | 1881-0942 | |
| dcterms.source.title | Heterocycles | |
| curtin.note |
Publisher can be found at: | |
| curtin.department | ||
| curtin.accessStatus | Open access |