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协同双金属镍/银和镍/铜催化烯基酮亚胺的区域选择性γ,δ-二芳基化:通过原位生成阳离子镍(II)催化剂解决β-H消除问题

Synergistic Bimetallic Ni/Ag and Ni/Cu Catalysis for Regioselective γ,δ-Diarylation of Alkenyl Ketimines: Addressing β-H Elimination by in Situ Generation of Cationic Ni(II) Catalysts.

作者信息

Basnet Prakash, Kc Shekhar, Dhungana Roshan K, Shrestha Bijay, Boyle Timothy J, Giri Ramesh

机构信息

Department of Chemistry & Chemical Biology , The University of New Mexico , Albuquerque , New Mexico 87131 , United States.

Sandia National Laboratory , Advanced Materials Laboratory , Albuquerque , New Mexico 87106 , United States.

出版信息

J Am Chem Soc. 2018 Nov 21;140(46):15586-15590. doi: 10.1021/jacs.8b09401. Epub 2018 Nov 6.

Abstract

We disclose unprecedented synergistic bimetallic Ni/Ag and Ni/Cu catalysts for regioselective γ,δ-diarylation of unactivated alkenes in simple ketimines with aryl halides and arylzinc reagents. The bimetallic synergy, which generates cationic Ni(II) species during reaction, promotes migratory insertion and transmetalation steps and suppresses β-H elimination and cross-coupling, the major side reactions that cause serious problems during alkene difunctionalization. This diarylation reaction proceeds at remote locations to imines to afford, after simple H workup, diversely substituted γ,δ-diaryl ketones that are otherwise difficult to access readily with existing methods.

摘要

我们公开了前所未有的协同双金属镍/银和镍/铜催化剂,用于在简单酮亚胺中,使未活化烯烃与芳基卤化物和芳基锌试剂进行区域选择性γ,δ-二芳基化反应。这种双金属协同作用在反应过程中生成阳离子镍(II)物种,促进迁移插入和转金属化步骤,并抑制β-氢消除和交叉偶联,这些是烯烃双官能化过程中导致严重问题的主要副反应。这种二芳基化反应在远离亚胺的位置进行,经过简单的加氢后处理,得到各种取代的γ,δ-二芳基酮,而这些酮用现有方法很难轻易获得。

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