Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds

Atom insertion into aromatic carbon-nitrogen (C-N) bonds is useful for the synthesis of nitrogen-containing molecules, but challenging due to the inert nature of these bonds. Here, the authors report one-carbon insertion into aromatic C-N bonds to directly convert anilines to chiral benzylic amines.

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Autores principales: Lei Li, Min Yang, Qiuqin He, Renhua Fan
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Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/917c54f7881d431788d492095569abd1
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spelling oai:doaj.org-article:917c54f7881d431788d492095569abd12021-12-02T18:48:04ZConversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds10.1038/s41467-020-18593-42041-1723https://doaj.org/article/917c54f7881d431788d492095569abd12020-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18593-4https://doaj.org/toc/2041-1723Atom insertion into aromatic carbon-nitrogen (C-N) bonds is useful for the synthesis of nitrogen-containing molecules, but challenging due to the inert nature of these bonds. Here, the authors report one-carbon insertion into aromatic C-N bonds to directly convert anilines to chiral benzylic amines.Lei LiMin YangQiuqin HeRenhua FanNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Lei Li
Min Yang
Qiuqin He
Renhua Fan
Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
description Atom insertion into aromatic carbon-nitrogen (C-N) bonds is useful for the synthesis of nitrogen-containing molecules, but challenging due to the inert nature of these bonds. Here, the authors report one-carbon insertion into aromatic C-N bonds to directly convert anilines to chiral benzylic amines.
format article
author Lei Li
Min Yang
Qiuqin He
Renhua Fan
author_facet Lei Li
Min Yang
Qiuqin He
Renhua Fan
author_sort Lei Li
title Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
title_short Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
title_full Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
title_fullStr Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
title_full_unstemmed Conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic C–N bonds
title_sort conversion of anilines to chiral benzylic amines via formal one-carbon insertion into aromatic c–n bonds
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/917c54f7881d431788d492095569abd1
work_keys_str_mv AT leili conversionofanilinestochiralbenzylicaminesviaformalonecarboninsertionintoaromaticcnbonds
AT minyang conversionofanilinestochiralbenzylicaminesviaformalonecarboninsertionintoaromaticcnbonds
AT qiuqinhe conversionofanilinestochiralbenzylicaminesviaformalonecarboninsertionintoaromaticcnbonds
AT renhuafan conversionofanilinestochiralbenzylicaminesviaformalonecarboninsertionintoaromaticcnbonds
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