The combination of asymmetric hydrogenation of olefins and direct reductive amination
Asymmetric hydrogenation (AH) and direct reductive amination (DRA) are both frequently utilized in chemical industry. Here, the authors combine these two transformations to efficiently convert in one step prochiral olefins into chiral amino compounds.
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2020-01-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-020-14475-x |
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doaj-28e77a9dfd754554b58a1a924478fd002021-05-11T08:26:32ZengNature Publishing GroupNature Communications2041-17232020-01-011111710.1038/s41467-020-14475-xThe combination of asymmetric hydrogenation of olefins and direct reductive aminationShuai Yuan0Guorui Gao1Lili Wang2Cungang Liu3Lei Wan4Haizhou Huang5Huiling Geng6Mingxin Chang7Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityCollege of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Shandong Normal UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityShaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F UniversityAsymmetric hydrogenation (AH) and direct reductive amination (DRA) are both frequently utilized in chemical industry. Here, the authors combine these two transformations to efficiently convert in one step prochiral olefins into chiral amino compounds.https://doi.org/10.1038/s41467-020-14475-x |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shuai Yuan Guorui Gao Lili Wang Cungang Liu Lei Wan Haizhou Huang Huiling Geng Mingxin Chang |
spellingShingle |
Shuai Yuan Guorui Gao Lili Wang Cungang Liu Lei Wan Haizhou Huang Huiling Geng Mingxin Chang The combination of asymmetric hydrogenation of olefins and direct reductive amination Nature Communications |
author_facet |
Shuai Yuan Guorui Gao Lili Wang Cungang Liu Lei Wan Haizhou Huang Huiling Geng Mingxin Chang |
author_sort |
Shuai Yuan |
title |
The combination of asymmetric hydrogenation of olefins and direct reductive amination |
title_short |
The combination of asymmetric hydrogenation of olefins and direct reductive amination |
title_full |
The combination of asymmetric hydrogenation of olefins and direct reductive amination |
title_fullStr |
The combination of asymmetric hydrogenation of olefins and direct reductive amination |
title_full_unstemmed |
The combination of asymmetric hydrogenation of olefins and direct reductive amination |
title_sort |
combination of asymmetric hydrogenation of olefins and direct reductive amination |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2020-01-01 |
description |
Asymmetric hydrogenation (AH) and direct reductive amination (DRA) are both frequently utilized in chemical industry. Here, the authors combine these two transformations to efficiently convert in one step prochiral olefins into chiral amino compounds. |
url |
https://doi.org/10.1038/s41467-020-14475-x |
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