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dc.contributor.authorLim, F.
dc.contributor.authorHalcovitch, N.
dc.contributor.authorTiekink, E.
dc.contributor.authorDolzhenko, Anton
dc.date.accessioned2018-05-18T08:01:01Z
dc.date.available2018-05-18T08:01:01Z
dc.date.created2018-05-18T00:22:54Z
dc.date.issued2018
dc.identifier.citationLim, 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.urihttp://hdl.handle.net/20.500.11937/68154
dc.identifier.doi10.1016/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.publisherPergamon-Elsevier Science Ltd
dc.titleA new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
dc.typeJournal Article
dcterms.source.volume74
dcterms.source.number15
dcterms.source.startPage1868
dcterms.source.endPage1879
dcterms.source.issn0040-4020
dcterms.source.titleTetrahedron
curtin.departmentSchool of Pharmacy and Biomedical Sciences
curtin.accessStatusFulltext not available


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