A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines

© 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 pur...

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Main Authors: Lim, F., Halcovitch, N., Tiekink, E., Dolzhenko, Anton
Format: Journal Article
Published: Pergamon-Elsevier Science Ltd 2018
Online Access:http://hdl.handle.net/20.500.11937/68154
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author Lim, F.
Halcovitch, N.
Tiekink, E.
Dolzhenko, Anton
author_facet Lim, F.
Halcovitch, N.
Tiekink, E.
Dolzhenko, Anton
author_sort Lim, F.
building Curtin Institutional Repository
collection Online Access
description © 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.
first_indexed 2025-11-14T10:36:44Z
format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:36:44Z
publishDate 2018
publisher Pergamon-Elsevier Science Ltd
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-681542018-05-18T08:07:30Z A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines Lim, F. Halcovitch, N. Tiekink, E. Dolzhenko, Anton © 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. 2018 Journal Article http://hdl.handle.net/20.500.11937/68154 10.1016/j.tet.2018.02.054 Pergamon-Elsevier Science Ltd restricted
spellingShingle Lim, F.
Halcovitch, N.
Tiekink, E.
Dolzhenko, Anton
A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title_full A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title_fullStr A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title_full_unstemmed A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title_short A new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: Selective synthesis of substituted 5-aza-9-deaza-adenines
title_sort new microwave-assisted, three-component reaction of 5-aminopyrazole-4-carboxylates: selective synthesis of substituted 5-aza-9-deaza-adenines
url http://hdl.handle.net/20.500.11937/68154