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Approaches towards the synthesis of 5-aminopyrazoles
The biological and medicinal properties of 5-aminopyrazoles have prompted enormous research aimed at developing synthetic routes to these heterocyles. This review focuses on the biological properties associated with this system. Various synthetic methods developed up to 2010 for these compounds are...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063075/ https://www.ncbi.nlm.nih.gov/pubmed/21448263 http://dx.doi.org/10.3762/bjoc.7.25 |
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author | Aggarwal, Ranjana Kumar, Vinod Kumar, Rajiv Singh, Shiv P |
author_facet | Aggarwal, Ranjana Kumar, Vinod Kumar, Rajiv Singh, Shiv P |
author_sort | Aggarwal, Ranjana |
collection | PubMed |
description | The biological and medicinal properties of 5-aminopyrazoles have prompted enormous research aimed at developing synthetic routes to these heterocyles. This review focuses on the biological properties associated with this system. Various synthetic methods developed up to 2010 for these compounds are described, particularly those that involve the reactions of β-ketonitriles, malononitrile, alkylidenemalononitriles and their derivatives with hydrazines, as well as some novel miscellaneous methods. |
format | Text |
id | pubmed-3063075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-30630752011-03-28 Approaches towards the synthesis of 5-aminopyrazoles Aggarwal, Ranjana Kumar, Vinod Kumar, Rajiv Singh, Shiv P Beilstein J Org Chem Review The biological and medicinal properties of 5-aminopyrazoles have prompted enormous research aimed at developing synthetic routes to these heterocyles. This review focuses on the biological properties associated with this system. Various synthetic methods developed up to 2010 for these compounds are described, particularly those that involve the reactions of β-ketonitriles, malononitrile, alkylidenemalononitriles and their derivatives with hydrazines, as well as some novel miscellaneous methods. Beilstein-Institut 2011-02-09 /pmc/articles/PMC3063075/ /pubmed/21448263 http://dx.doi.org/10.3762/bjoc.7.25 Text en Copyright © 2011, Aggarwal et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), 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, Vinod Kumar, Rajiv Singh, Shiv P Approaches towards the synthesis of 5-aminopyrazoles |
title | Approaches towards the synthesis of 5-aminopyrazoles |
title_full | Approaches towards the synthesis of 5-aminopyrazoles |
title_fullStr | Approaches towards the synthesis of 5-aminopyrazoles |
title_full_unstemmed | Approaches towards the synthesis of 5-aminopyrazoles |
title_short | Approaches towards the synthesis of 5-aminopyrazoles |
title_sort | approaches towards the synthesis of 5-aminopyrazoles |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063075/ https://www.ncbi.nlm.nih.gov/pubmed/21448263 http://dx.doi.org/10.3762/bjoc.7.25 |
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