Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation
Hydroformylation of 1,2-disubstituted alkenes usually occurs at the α position of the directing heteroatom. Here, the authors report the asymmetric rhodium-catalyzed hydroformylation of 1,2-disubstituted alkenylsilanes with excellent regioselectivity at the β position (relative to the silicon hetero...
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2018-05-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-04277-7 |
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doaj-8a8889051f1e44aa88f300938dd4c0c12021-05-11T09:22:20ZengNature Publishing GroupNature Communications2041-17232018-05-01911910.1038/s41467-018-04277-7Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylationCai You0Xiuxiu Li1Yuhong Yang2Yu-Sheng Yang3Xuefeng Tan4Shuailong Li5Biao Wei6Hui Lv7Lung-Wa Chung8Xumu Zhang9Key Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityDepartment of Chemistry, Southern University of Science and Technology, ShenzhenKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityDepartment of Chemistry, Southern University of Science and Technology, ShenzhenKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityDepartment of Chemistry, Southern University of Science and Technology, ShenzhenKey Laboratory of Biomedical Polymers of Ministry of Education & College of Chemistry and Molecular Sciences, Wuhan UniversityHydroformylation of 1,2-disubstituted alkenes usually occurs at the α position of the directing heteroatom. Here, the authors report the asymmetric rhodium-catalyzed hydroformylation of 1,2-disubstituted alkenylsilanes with excellent regioselectivity at the β position (relative to the silicon heteroatom) and enantioselectivity.https://doi.org/10.1038/s41467-018-04277-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Cai You Xiuxiu Li Yuhong Yang Yu-Sheng Yang Xuefeng Tan Shuailong Li Biao Wei Hui Lv Lung-Wa Chung Xumu Zhang |
spellingShingle |
Cai You Xiuxiu Li Yuhong Yang Yu-Sheng Yang Xuefeng Tan Shuailong Li Biao Wei Hui Lv Lung-Wa Chung Xumu Zhang Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation Nature Communications |
author_facet |
Cai You Xiuxiu Li Yuhong Yang Yu-Sheng Yang Xuefeng Tan Shuailong Li Biao Wei Hui Lv Lung-Wa Chung Xumu Zhang |
author_sort |
Cai You |
title |
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
title_short |
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
title_full |
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
title_fullStr |
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
title_full_unstemmed |
Silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
title_sort |
silicon-oriented regio- and enantioselective rhodium-catalyzed hydroformylation |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2018-05-01 |
description |
Hydroformylation of 1,2-disubstituted alkenes usually occurs at the α position of the directing heteroatom. Here, the authors report the asymmetric rhodium-catalyzed hydroformylation of 1,2-disubstituted alkenylsilanes with excellent regioselectivity at the β position (relative to the silicon heteroatom) and enantioselectivity. |
url |
https://doi.org/10.1038/s41467-018-04277-7 |
work_keys_str_mv |
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