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5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines

The condensation of 5-aminopyrazole with various bielectrophilic moieties results in the formation of pyrazoloazines, an interesting array of fused heterocyclic systems. The development of new synthetic routes towards pyrazoloazines for their biological and medicinal exploration is an attractive are...

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Detalles Bibliográficos
Autores principales: Aggarwal, Ranjana, Kumar, Suresh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789427/
https://www.ncbi.nlm.nih.gov/pubmed/29441143
http://dx.doi.org/10.3762/bjoc.14.15
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author Aggarwal, Ranjana
Kumar, Suresh
author_facet Aggarwal, Ranjana
Kumar, Suresh
author_sort Aggarwal, Ranjana
collection PubMed
description The condensation of 5-aminopyrazole with various bielectrophilic moieties results in the formation of pyrazoloazines, an interesting array of fused heterocyclic systems. The development of new synthetic routes towards pyrazoloazines for their biological and medicinal exploration is an attractive area for researchers throughout the world. The present review focuses on various synthetic methods developed in the last decade for the synthesis of differently substituted pyrazoloazines by a broad range of organic reactions by means of 5-aminopyrazole as a precursor.
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spelling pubmed-57894272018-02-13 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines Aggarwal, Ranjana Kumar, Suresh Beilstein J Org Chem Review The condensation of 5-aminopyrazole with various bielectrophilic moieties results in the formation of pyrazoloazines, an interesting array of fused heterocyclic systems. The development of new synthetic routes towards pyrazoloazines for their biological and medicinal exploration is an attractive area for researchers throughout the world. The present review focuses on various synthetic methods developed in the last decade for the synthesis of differently substituted pyrazoloazines by a broad range of organic reactions by means of 5-aminopyrazole as a precursor. Beilstein-Institut 2018-01-25 /pmc/articles/PMC5789427/ /pubmed/29441143 http://dx.doi.org/10.3762/bjoc.14.15 Text en Copyright © 2018, Aggarwal and Kumar https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Aggarwal, Ranjana
Kumar, Suresh
5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title_full 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title_fullStr 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title_full_unstemmed 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title_short 5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
title_sort 5-aminopyrazole as precursor in design and synthesis of fused pyrazoloazines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789427/
https://www.ncbi.nlm.nih.gov/pubmed/29441143
http://dx.doi.org/10.3762/bjoc.14.15
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