Lewis Base–Boryl Radicals Enabled Borylation Reactions and Selective Activation of Carbon–Heteroatom Bonds-Reference-Cited by-同舟云学术

Lewis Base–Boryl Radicals Enabled Borylation Reactions and Selective Activation of Carbon–Heteroatom Bonds

Published:2022-12-26 Issue:2 Volume:56 Page:169-186
ISSN:0001-4842
Container-title:Accounts of Chemical Research
language:en
Short-container-title:Acc. Chem. Res.

Author:

Peng Tian-Yu¹,Zhang Feng-Lian¹,Wang Yi-Feng¹²^ORCID

Affiliation:

1. Hefei National Research Center for Physical Sciences at the Microscale, Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, 230026 Anhui, China

2. State Key Laboratory of Elemento-Organic Chemistry, Nankai University, 94 Weijin Road, Tianjin 300071, China

Funder

Central University Basic Research Fund of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

General Medicine,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.accounts.2c00752

Reference77 articles.

1. Radical Borylation/Cyclization Cascade of 1,6-Enynes for the Synthesis of Boron-Handled Hetero- and Carbocycles

2. New Radical Borylation Pathways for Organoboron Synthesis Enabled by Photoredox Catalysis

3. Sequential C–F bond functionalizations of trifluoroacetamides and acetates via spin-center shifts

4. Boryl Radicals Enabled a Three-Step Sequence to Assemble All-Carbon Quaternary Centers from Activated Trichloromethyl Groups

5. Radicals: Reactive Intermediates with Translational Potential

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