Selective Coupling of 1,2‐Bis‐Boronic Esters at the more Substituted Site through Visible‐Light Activation of Electron Donor–Acceptor Complexes-Reference-Cited by-同舟云学术

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Selective Coupling of 1,2‐Bis‐Boronic Esters at the more Substituted Site through Visible‐Light Activation of Electron Donor–Acceptor Complexes

Published:2022-03-07 Issue:18 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Wang Hui¹^ORCID,Wu Jingjing¹²^ORCID,Noble Adam¹^ORCID,Aggarwal Varinder K.¹^ORCID

Affiliation:

1. School of Chemistry University of Bristol, Cantock's Close Bristol BS8 1TS UK

2. Current address: Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering Shanghai Jiaotong University No. 800, Dongchuan Road Shanghai 200240 China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202202061

Reference80 articles.

2. Boron Reagents in Process Chemistry: Excellent Tools for Selective Reductions

3. Lithiation–Borylation Methodology and Its Application in Synthesis

4. Asymmetric Synthesis of Secondary and Tertiary Boronic Esters

5. Asymmetrische Synthese sekundärer und tertiärer Boronsäureester

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Alkoxide-Assisted Stereoselective Functionalization of 1,2-Bis-boronic Esters Under Photoredox Catalysis;Organic Letters;2024-07-25

2. An in situ generated proton initiated aromatic fluoroalkylation via electron donor–acceptor complex photoactivation;Green Chemistry;2024

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