Modular Synthesis of Chiral Tetrasubstituted Allylic Amines via Nickel-Catalyzed Enantioselective Difunctionalization of Alkynes with Imines and Arylboronic Acids

-sulfonylimines and arylboronic reagents. This asymmetric three-component transformation furnished a wide range of enantioenriched tetrasubstituted allylic amines with excellent regioselectivity and stereoselectivity under mild conditions.

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Publication Details

Journal
Organic Letters
Published
2026-04-27
DOI
https://doi.org/10.1021/acs.orglett.6c01015
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Modular Synthesis of Chiral Tetrasubstituted Allylic Amines via Nickel-Catalyzed Enantioselective Difunctionalization of Alkynes with Imines and Arylboronic Acids

Fangfang Feng, Haitao Yu, Zhuojia Hou, Shuojia Li et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Modular Synthesis of Chiral Tetrasubstituted Allylic Amines via Nickel-Catalyzed Enantioselective Difunctionalization of Alkynes with Imines and Arylboronic Acids

Fangfang Feng, Haitao Yu, Zhuojia Hou, Shuojia Li, Xiaojuan Wang, Xiruo Han, Yongbing Liu
article en

Abstract

-sulfonylimines and arylboronic reagents. This asymmetric three-component transformation furnished a wide range of enantioenriched tetrasubstituted allylic amines with excellent regioselectivity and stereoselectivity under mild conditions.

Organic LettersVol. 28(18)
Laboratoire de Synthèse Organique (FR), Advanced Materials and Devices (United States) (US), Hebei Normal University (CN)
Hebei Normal University, Natural Science Foundation of Hebei Province, Hebei Provincial Department of Bureau of Science and Technology
Openalex Percentile: Top 18%
Catalytic C–H Functionalization Methods
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