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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
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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. |
format | Online Article Text |
id | pubmed-5789427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT aggarwalranjana 5aminopyrazoleasprecursorindesignandsynthesisoffusedpyrazoloazines AT kumarsuresh 5aminopyrazoleasprecursorindesignandsynthesisoffusedpyrazoloazines |