Practical synthesis of regioisomeric 5(7)-amino-6,7(4,5)-dihydro[1,2,4]triazolo[1,5-a][1,3,5]triazines
dc.contributor.author | Dolzhenko, Anton | |
dc.contributor.author | Dolzhenko, A. | |
dc.contributor.author | Chui, W. | |
dc.date.accessioned | 2017-01-30T12:19:32Z | |
dc.date.available | 2017-01-30T12:19:32Z | |
dc.date.created | 2011-08-24T20:01:11Z | |
dc.date.issued | 2007 | |
dc.identifier.citation | Dolzhenko, Anton and Dolzhenko, Anna and Chui, Wai. 2007. Practical synthesis of regioisomeric 5(7)-amino-6,7(4,5)-dihydro[1,2,4]triazolo[1,5-a][1,3,5]triazines. Tetrahedron. 63 (52): pp. 12888-12895. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/20487 | |
dc.identifier.doi | 10.1016/j.tet.2007.10.046 | |
dc.description.abstract |
A convenient and efficient synthesis of new 5-azapurine derivatives was developed. The regioisomeric 5-amino-6,7-dihydro- and 7-amino-4,5-dihydro[1,2,4]triazolo[1,5-a][1,3,5]triazines were prepared in 3?4 steps from benzhydrazide via complementary and regiospecific routes as a part of our lead finding program. The molecular structures and tautomeric preferences of the compounds obtained were investigated using NMR spectral data and X-ray crystallography. | |
dc.publisher | Pergamon-Elsevier Science Ltd | |
dc.title | Practical synthesis of regioisomeric 5(7)-amino-6,7(4,5)-dihydro[1,2,4]triazolo[1,5-a][1,3,5]triazines | |
dc.type | Journal Article | |
dcterms.source.volume | 63 | |
dcterms.source.number | 52 | |
dcterms.source.startPage | 12888 | |
dcterms.source.endPage | 12895 | |
dcterms.source.issn | 00404020 | |
dcterms.source.title | Tetrahedron | |
curtin.note |
NOTICE: This is the author's version of a work that was accepted for publication in Tetrahedron. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron, 63, 52, 2007. DOI: 10.1016/j.tet.2007.10.046 | |
curtin.department | School of Pharmacy | |
curtin.accessStatus | Open access |