A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
dc.contributor.author | Lim, F. | |
dc.contributor.author | Halcovitch, N. | |
dc.contributor.author | Tiekink, E. | |
dc.contributor.author | Dolzhenko, Anton | |
dc.date.accessioned | 2018-05-18T08:01:01Z | |
dc.date.available | 2018-05-18T08:01:01Z | |
dc.date.created | 2018-05-18T00:22:54Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Lim, F. and Halcovitch, N. and Tiekink, E. and Dolzhenko, A. 2018. A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines. Tetrahedron. 74 (15): pp. 1868-1879. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/68154 | |
dc.identifier.doi | 10.1016/j.tet.2018.02.054 | |
dc.description.abstract |
© 2018 Elsevier Ltd A series of 5-aza-9-deaza- analogues of purine was effectively prepared using highly selective annulation of 1,3,5-triazine ring onto 5-aminopyrazole-4-carboxylates via a one-pot, multicomponent, microwave-assisted approach. The products were obtained in good yields and high purity. This catalyst-free method was demonstrated to be scalable and highly reproducible in different microwave reactors. Some structural features of the prepared compounds were studied in details using dynamic NMR spectroscopy and X-ray crystallography. | |
dc.publisher | Pergamon-Elsevier Science Ltd | |
dc.title | A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines | |
dc.type | Journal Article | |
dcterms.source.volume | 74 | |
dcterms.source.number | 15 | |
dcterms.source.startPage | 1868 | |
dcterms.source.endPage | 1879 | |
dcterms.source.issn | 0040-4020 | |
dcterms.source.title | Tetrahedron | |
curtin.department | School of Pharmacy and Biomedical Sciences | |
curtin.accessStatus | Fulltext not available |
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