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Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation
[Image: see text] Deoxygenative hydrogenation of amides to amines homogeneously catalyzed by a complex of an Earth-abundant metal is presented. This manganese-catalyzed reaction features high efficiency and selectivity. A plausible reaction mechanism, involving metal–ligand cooperation of the mangan...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503579/ https://www.ncbi.nlm.nih.gov/pubmed/31080688 http://dx.doi.org/10.1021/acscatal.8b02902 |
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author | Zou, You-Quan Chakraborty, Subrata Nerush, Alexander Oren, Dror Diskin-Posner, Yael Ben-David, Yehoshoa Milstein, David |
author_facet | Zou, You-Quan Chakraborty, Subrata Nerush, Alexander Oren, Dror Diskin-Posner, Yael Ben-David, Yehoshoa Milstein, David |
author_sort | Zou, You-Quan |
collection | PubMed |
description | [Image: see text] Deoxygenative hydrogenation of amides to amines homogeneously catalyzed by a complex of an Earth-abundant metal is presented. This manganese-catalyzed reaction features high efficiency and selectivity. A plausible reaction mechanism, involving metal–ligand cooperation of the manganese pincer complex, is proposed based on NMR studies and relevant stoichiometric reactions. |
format | Online Article Text |
id | pubmed-6503579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65035792019-05-08 Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation Zou, You-Quan Chakraborty, Subrata Nerush, Alexander Oren, Dror Diskin-Posner, Yael Ben-David, Yehoshoa Milstein, David ACS Catal [Image: see text] Deoxygenative hydrogenation of amides to amines homogeneously catalyzed by a complex of an Earth-abundant metal is presented. This manganese-catalyzed reaction features high efficiency and selectivity. A plausible reaction mechanism, involving metal–ligand cooperation of the manganese pincer complex, is proposed based on NMR studies and relevant stoichiometric reactions. American Chemical Society 2018-07-30 2018-09-07 /pmc/articles/PMC6503579/ /pubmed/31080688 http://dx.doi.org/10.1021/acscatal.8b02902 Text en Copyright © 2018 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 | Zou, You-Quan Chakraborty, Subrata Nerush, Alexander Oren, Dror Diskin-Posner, Yael Ben-David, Yehoshoa Milstein, David Highly Selective, Efficient Deoxygenative Hydrogenation of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title | Highly Selective, Efficient Deoxygenative Hydrogenation
of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title_full | Highly Selective, Efficient Deoxygenative Hydrogenation
of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title_fullStr | Highly Selective, Efficient Deoxygenative Hydrogenation
of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title_full_unstemmed | Highly Selective, Efficient Deoxygenative Hydrogenation
of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title_short | Highly Selective, Efficient Deoxygenative Hydrogenation
of Amides Catalyzed by a Manganese Pincer Complex via Metal–Ligand Cooperation |
title_sort | highly selective, efficient deoxygenative hydrogenation
of amides catalyzed by a manganese pincer complex via metal–ligand cooperation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503579/ https://www.ncbi.nlm.nih.gov/pubmed/31080688 http://dx.doi.org/10.1021/acscatal.8b02902 |
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