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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...

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Detalles Bibliográficos
Autores principales: Kamal, Mohammad M., Liu, Zhizhou, Zhai, Siyuan, Vidović, Dragoslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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
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