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Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane

[Image: see text] A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as catalyst and ammonia-borane as transfer agent has been developed. This transformation represents a unique example of low-valent pnictogen catalysis cycling between oxidation states I and III, and proved us...

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Autores principales: Wang, Feng, Planas, Oriol, Cornella, Josep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728098/
https://www.ncbi.nlm.nih.gov/pubmed/30816708
http://dx.doi.org/10.1021/jacs.9b00594
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author Wang, Feng
Planas, Oriol
Cornella, Josep
author_facet Wang, Feng
Planas, Oriol
Cornella, Josep
author_sort Wang, Feng
collection PubMed
description [Image: see text] A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as catalyst and ammonia-borane as transfer agent has been developed. This transformation represents a unique example of low-valent pnictogen catalysis cycling between oxidation states I and III, and proved useful for the hydrogenation of azoarenes and the partial reduction of nitroarenes. Interestingly, the bismuthinidene catalyst performs well in the presence of low-valent transition-metal sensitive functional groups and presents orthogonal reactivity compared to analogous phosphorus-based catalysis. Mechanistic investigations suggest the intermediacy of an elusive bismuthine species, which is proposed to be responsible for the hydrogenation and the formation of hydrogen.
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spelling pubmed-67280982019-09-06 Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane Wang, Feng Planas, Oriol Cornella, Josep J Am Chem Soc [Image: see text] A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as catalyst and ammonia-borane as transfer agent has been developed. This transformation represents a unique example of low-valent pnictogen catalysis cycling between oxidation states I and III, and proved useful for the hydrogenation of azoarenes and the partial reduction of nitroarenes. Interestingly, the bismuthinidene catalyst performs well in the presence of low-valent transition-metal sensitive functional groups and presents orthogonal reactivity compared to analogous phosphorus-based catalysis. Mechanistic investigations suggest the intermediacy of an elusive bismuthine species, which is proposed to be responsible for the hydrogenation and the formation of hydrogen. American Chemical Society 2019-02-28 2019-03-13 /pmc/articles/PMC6728098/ /pubmed/30816708 http://dx.doi.org/10.1021/jacs.9b00594 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Wang, Feng
Planas, Oriol
Cornella, Josep
Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title_full Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title_fullStr Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title_full_unstemmed Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title_short Bi(I)-Catalyzed Transfer-Hydrogenation with Ammonia-Borane
title_sort bi(i)-catalyzed transfer-hydrogenation with ammonia-borane
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6728098/
https://www.ncbi.nlm.nih.gov/pubmed/30816708
http://dx.doi.org/10.1021/jacs.9b00594
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