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Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones
[Image: see text] We disclose the synthesis of a series of manganese complexes of chiral iminopyridine oxazoline ligands and their application in the first manganese-catalyzed asymmetric ketone hydrosilylations. The most sterically hindered manganese catalyst bearing two CH(Ph)(2) groups at the 2,6-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641774/ https://www.ncbi.nlm.nih.gov/pubmed/31457754 http://dx.doi.org/10.1021/acsomega.7b00713 |
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author | Ma, Xiaochen Zuo, Ziqing Liu, Guixia Huang, Zheng |
author_facet | Ma, Xiaochen Zuo, Ziqing Liu, Guixia Huang, Zheng |
author_sort | Ma, Xiaochen |
collection | PubMed |
description | [Image: see text] We disclose the synthesis of a series of manganese complexes of chiral iminopyridine oxazoline ligands and their application in the first manganese-catalyzed asymmetric ketone hydrosilylations. The most sterically hindered manganese catalyst bearing two CH(Ph)(2) groups at the 2,6-ortho positions of the imino aryl ring and a tBu group on the oxazoline ring furnishes the secondary alcohols in high enantioselectivities and yields. |
format | Online Article Text |
id | pubmed-6641774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66417742019-08-27 Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones Ma, Xiaochen Zuo, Ziqing Liu, Guixia Huang, Zheng ACS Omega [Image: see text] We disclose the synthesis of a series of manganese complexes of chiral iminopyridine oxazoline ligands and their application in the first manganese-catalyzed asymmetric ketone hydrosilylations. The most sterically hindered manganese catalyst bearing two CH(Ph)(2) groups at the 2,6-ortho positions of the imino aryl ring and a tBu group on the oxazoline ring furnishes the secondary alcohols in high enantioselectivities and yields. American Chemical Society 2017-08-18 /pmc/articles/PMC6641774/ /pubmed/31457754 http://dx.doi.org/10.1021/acsomega.7b00713 Text en Copyright © 2017 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 | Ma, Xiaochen Zuo, Ziqing Liu, Guixia Huang, Zheng Manganese-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones |
title | Manganese-Catalyzed Asymmetric Hydrosilylation of
Aryl Ketones |
title_full | Manganese-Catalyzed Asymmetric Hydrosilylation of
Aryl Ketones |
title_fullStr | Manganese-Catalyzed Asymmetric Hydrosilylation of
Aryl Ketones |
title_full_unstemmed | Manganese-Catalyzed Asymmetric Hydrosilylation of
Aryl Ketones |
title_short | Manganese-Catalyzed Asymmetric Hydrosilylation of
Aryl Ketones |
title_sort | manganese-catalyzed asymmetric hydrosilylation of
aryl ketones |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641774/ https://www.ncbi.nlm.nih.gov/pubmed/31457754 http://dx.doi.org/10.1021/acsomega.7b00713 |
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