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Imine Reduction with Me(2)S-BH(3)
Although there exists a variety of different catalysts for hydroboration of organic substrates such as aldehydes, ketones, imines, nitriles etc., recent evidence suggests that tetra-coordinate borohydride species, formed by activation, redistribution, or decomposition of boron reagents, are the true...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467297/ https://www.ncbi.nlm.nih.gov/pubmed/34576911 http://dx.doi.org/10.3390/molecules26185443 |
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author | Kamal, Mohammad M. Liu, Zhizhou Zhai, Siyuan Vidović, Dragoslav |
author_facet | Kamal, Mohammad M. Liu, Zhizhou Zhai, Siyuan Vidović, Dragoslav |
author_sort | Kamal, Mohammad M. |
collection | PubMed |
description | Although there exists a variety of different catalysts for hydroboration of organic substrates such as aldehydes, ketones, imines, nitriles etc., recent evidence suggests that tetra-coordinate borohydride species, formed by activation, redistribution, or decomposition of boron reagents, are the true hydride donors. We then proposed that Me(2)S-BH(3) could also act as a hydride donor for the reduction of various imines, as similar compounds have been observed to reduce carbonyl substrates. This boron reagent was shown to be an effective and chemoselective hydroboration reagent for a wide variety of imines. |
format | Online Article Text |
id | pubmed-8467297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84672972021-09-27 Imine Reduction with Me(2)S-BH(3) Kamal, Mohammad M. Liu, Zhizhou Zhai, Siyuan Vidović, Dragoslav Molecules Communication Although there exists a variety of different catalysts for hydroboration of organic substrates such as aldehydes, ketones, imines, nitriles etc., recent evidence suggests that tetra-coordinate borohydride species, formed by activation, redistribution, or decomposition of boron reagents, are the true hydride donors. We then proposed that Me(2)S-BH(3) could also act as a hydride donor for the reduction of various imines, as similar compounds have been observed to reduce carbonyl substrates. This boron reagent was shown to be an effective and chemoselective hydroboration reagent for a wide variety of imines. MDPI 2021-09-07 /pmc/articles/PMC8467297/ /pubmed/34576911 http://dx.doi.org/10.3390/molecules26185443 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Kamal, Mohammad M. Liu, Zhizhou Zhai, Siyuan Vidović, Dragoslav Imine Reduction with Me(2)S-BH(3) |
title | Imine Reduction with Me(2)S-BH(3) |
title_full | Imine Reduction with Me(2)S-BH(3) |
title_fullStr | Imine Reduction with Me(2)S-BH(3) |
title_full_unstemmed | Imine Reduction with Me(2)S-BH(3) |
title_short | Imine Reduction with Me(2)S-BH(3) |
title_sort | imine reduction with me(2)s-bh(3) |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467297/ https://www.ncbi.nlm.nih.gov/pubmed/34576911 http://dx.doi.org/10.3390/molecules26185443 |
work_keys_str_mv | AT kamalmohammadm iminereductionwithme2sbh3 AT liuzhizhou iminereductionwithme2sbh3 AT zhaisiyuan iminereductionwithme2sbh3 AT vidovicdragoslav iminereductionwithme2sbh3 |