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Benzhydryl Amines: Synthesis and Their Biological Perspective
[Image: see text] The current review describes the recent progress in the chemistry and biology of the benzhydryl amines where the central carbon atom is directly attached to the nitrogen atom of one ring and which have published in the last five years (2015–2019). Both metal and metal-free racemic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963937/ https://www.ncbi.nlm.nih.gov/pubmed/31956747 http://dx.doi.org/10.1021/acsomega.9b03090 |
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author | Roy, Deblina Panda, Gautam |
author_facet | Roy, Deblina Panda, Gautam |
author_sort | Roy, Deblina |
collection | PubMed |
description | [Image: see text] The current review describes the recent progress in the chemistry and biology of the benzhydryl amines where the central carbon atom is directly attached to the nitrogen atom of one ring and which have published in the last five years (2015–2019). Both metal and metal-free racemic and asymmetric synthetic approaches along with their activities as anti-leishmanial, antiviral, antibacterial, and anti-aromatase and other miscellaneous properties are discussed. |
format | Online Article Text |
id | pubmed-6963937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69639372020-01-17 Benzhydryl Amines: Synthesis and Their Biological Perspective Roy, Deblina Panda, Gautam ACS Omega [Image: see text] The current review describes the recent progress in the chemistry and biology of the benzhydryl amines where the central carbon atom is directly attached to the nitrogen atom of one ring and which have published in the last five years (2015–2019). Both metal and metal-free racemic and asymmetric synthetic approaches along with their activities as anti-leishmanial, antiviral, antibacterial, and anti-aromatase and other miscellaneous properties are discussed. American Chemical Society 2019-12-17 /pmc/articles/PMC6963937/ /pubmed/31956747 http://dx.doi.org/10.1021/acsomega.9b03090 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Roy, Deblina Panda, Gautam Benzhydryl Amines: Synthesis and Their Biological Perspective |
title | Benzhydryl Amines:
Synthesis and Their Biological
Perspective |
title_full | Benzhydryl Amines:
Synthesis and Their Biological
Perspective |
title_fullStr | Benzhydryl Amines:
Synthesis and Their Biological
Perspective |
title_full_unstemmed | Benzhydryl Amines:
Synthesis and Their Biological
Perspective |
title_short | Benzhydryl Amines:
Synthesis and Their Biological
Perspective |
title_sort | benzhydryl amines:
synthesis and their biological
perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963937/ https://www.ncbi.nlm.nih.gov/pubmed/31956747 http://dx.doi.org/10.1021/acsomega.9b03090 |
work_keys_str_mv | AT roydeblina benzhydrylaminessynthesisandtheirbiologicalperspective AT pandagautam benzhydrylaminessynthesisandtheirbiologicalperspective |