Copper-Catalyzed Enantioselective Decarboxylative Cyanation of Benzylic Acids Promoted by Hypervalent Iodine(III) Reagents
Author:
Affiliation:
1. Henan Institute of Advanced Technology, College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China
2. High & New Technology Research Center, Henan Academy of Sciences, Zhengzhou 450002, P. R. China
Funder
State Key Laboratory of Bio-organic and Natural Products Chemistry
Zhengzhou University
China Postdoctoral Science Foundation
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c00816
Reference66 articles.
1. Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
2. Decarboxylation as the Key Step in C−C Bond-Forming Reactions
3. Decarboxylative reactions with and without light – a comparison
4. Decarboxylation‐Initiated Intermolecular Carbon‐Heteroatom Bond Formation
5. Carboxylic Acids as Adaptive Functional Groups in Metallaphotoredox Catalysis
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2. Copper-Catalyzed Asymmetric Cyanation of Propargylic Radicals via Direct Decarboxylation of Propargylic Carboxylic Acids;Organic Letters;2023-06-29
3. Progress in Synthesis of Sulfonyl Fluoride;Journal of Organic Chemistry Research;2023
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