Borylation of Olefin C-H Bond via Aryl to Vinyl Palladium 1,4-Migration

Journal of the American Chemical Society
Tian-Jiao HuGuo-Qiang Lin

Abstract

The aryl to vinyl palladium 1,4-migration was realized for the first time. The generated alkenyl palladium species was trapped by diboron reagents under Miyaura borylation conditions, providing a new method to synthesize β,β-disubstituted vinylboronates. The excellent regioselectivity and broad substrate scope were observed for this novel transformation.

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Citations

Dec 23, 2016·Chemical Communications : Chem Comm·Ebrahim-Alkhalil M A AhmedYao Fu
Jan 23, 2018·Chemistry : a European Journal·Johnathon D Dooley, Hon Wai Lam
Sep 4, 2018·Chemical Communications : Chem Comm·Bo ZhouYanghui Zhang
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Jul 29, 2017·Angewandte Chemie·Zhuo WuYanghui Zhang
Sep 4, 2019·Chemical Communications : Chem Comm·Luke O'BrienHon Wai Lam
Nov 5, 2020·Chemical Communications : Chem Comm·Ze-Jian XueGuo-Qiang Lin
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May 16, 2019·Journal of the American Chemical Society·Benedikt S Schreib, Erick M Carreira
Aug 28, 2021·Chemical Reviews·Tomáš NeveselýRyan Gilmour

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