Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations

Chiral aliphatic amine and alcohol derivatives are difficult to access due to the challenge to differentiate between spatially and electronically similar alkyl groups. Here the authors show a nickel-catalyzed enantioselective hydroalkylation of acyl enamines and enol esters with alkyl halides to aff...

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Autores principales: Shan Wang, Jian-Xin Zhang, Tian-Yi Zhang, Huan Meng, Bi-Hong Chen, Wei Shu
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Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/b09c196bb05141289813ae569bf9f442
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spelling oai:doaj.org-article:b09c196bb05141289813ae569bf9f4422021-12-02T16:50:35ZEnantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations10.1038/s41467-021-22983-72041-1723https://doaj.org/article/b09c196bb05141289813ae569bf9f4422021-05-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-22983-7https://doaj.org/toc/2041-1723Chiral aliphatic amine and alcohol derivatives are difficult to access due to the challenge to differentiate between spatially and electronically similar alkyl groups. Here the authors show a nickel-catalyzed enantioselective hydroalkylation of acyl enamines and enol esters with alkyl halides to afford enantioenriched α-branched aliphatic acyl amines and esters in good yields with excellent enantioselectivity.Shan WangJian-Xin ZhangTian-Yi ZhangHuan MengBi-Hong ChenWei ShuNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Shan Wang
Jian-Xin Zhang
Tian-Yi Zhang
Huan Meng
Bi-Hong Chen
Wei Shu
Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
description Chiral aliphatic amine and alcohol derivatives are difficult to access due to the challenge to differentiate between spatially and electronically similar alkyl groups. Here the authors show a nickel-catalyzed enantioselective hydroalkylation of acyl enamines and enol esters with alkyl halides to afford enantioenriched α-branched aliphatic acyl amines and esters in good yields with excellent enantioselectivity.
format article
author Shan Wang
Jian-Xin Zhang
Tian-Yi Zhang
Huan Meng
Bi-Hong Chen
Wei Shu
author_facet Shan Wang
Jian-Xin Zhang
Tian-Yi Zhang
Huan Meng
Bi-Hong Chen
Wei Shu
author_sort Shan Wang
title Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
title_short Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
title_full Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
title_fullStr Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
title_full_unstemmed Enantioselective access to chiral aliphatic amines and alcohols via Ni-catalyzed hydroalkylations
title_sort enantioselective access to chiral aliphatic amines and alcohols via ni-catalyzed hydroalkylations
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b09c196bb05141289813ae569bf9f442
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AT jianxinzhang enantioselectiveaccesstochiralaliphaticaminesandalcoholsvianicatalyzedhydroalkylations
AT tianyizhang enantioselectiveaccesstochiralaliphaticaminesandalcoholsvianicatalyzedhydroalkylations
AT huanmeng enantioselectiveaccesstochiralaliphaticaminesandalcoholsvianicatalyzedhydroalkylations
AT bihongchen enantioselectiveaccesstochiralaliphaticaminesandalcoholsvianicatalyzedhydroalkylations
AT weishu enantioselectiveaccesstochiralaliphaticaminesandalcoholsvianicatalyzedhydroalkylations
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