Synthesis and structure of 3,4-dihydropyrido[2’,3’:3,4]pyrazolo[1,5-a][1,3,5]triazin-2-amines
| dc.contributor.author | Dolzhenko, Anton | |
| dc.contributor.author | Bai, S. | |
| dc.contributor.author | Dolzhenko, A. | |
| dc.contributor.author | Chui, W. | |
| dc.date.accessioned | 2017-01-30T10:29:04Z | |
| dc.date.available | 2017-01-30T10:29:04Z | |
| dc.date.created | 2012-09-11T20:01:15Z | |
| dc.date.issued | 2012 | |
| dc.identifier.citation | Dolzhenko, Anton V. and Bai, Shiqi and Dolzhenko, Anna V. and Chui, Wai Keung. 2012. Synthesis and structure of 3,4-dihydropyrido[2’,3’:3,4]pyrazolo[1,5-a][1,3,5]triazin-2-amines. Journal of Heterocyclic Chemistry. 49 (4): pp. 763-767. | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11937/3152 | |
| dc.identifier.doi | 10.1002/jhet.851 | |
| dc.description.abstract |
A new convenient synthon for heterocyclic chemistry, namely 1H-pyrazolo[3,4-b]pyridin-3-ylguanidine was successfully prepared by selective guanylation of 1H-pyrazolo[3,4-b]pyridin-3-amine. A series of 3,4-dihydropyrido[2′,3′:3,4]pyrazolo[1,5-a][1,3,5]triazin-2-amines was synthesized from 1H-pyrazolo[3,4-b]pyridin-3-ylguanidine using aldehydes or ketones as one-carbon inserting reagents. The tautomeric preferences of the products were determined using spectroscopic (e.g., 2D NOESY NMR) and single crystal X-ray diffraction data. | |
| dc.publisher | John Wiley & Sons | |
| dc.subject | pyridines | |
| dc.subject | triazines | |
| dc.subject | guanidines | |
| dc.subject | tautomerism | |
| dc.subject | pyrazoles | |
| dc.title | Synthesis and structure of 3,4-dihydropyrido[2’,3’:3,4]pyrazolo[1,5-a][1,3,5]triazin-2-amines | |
| dc.type | Journal Article | |
| dcterms.source.volume | 48 | |
| dcterms.source.number | 4 | |
| dcterms.source.startPage | 763 | |
| dcterms.source.endPage | 767 | |
| dcterms.source.issn | 0022-152X | |
| dcterms.source.title | Journal of Heterocyclic Chemistry | |
| curtin.department | ||
| curtin.accessStatus | Fulltext not available |