Use of the 2-Pyridinesulfonyloxy Leaving Group for the Fast Copper-Catalyzed Coupling Reaction at Secondary Alkyl Carbons with Grignard Reagents
Author:
Affiliation:
1. Department of Bioengineering, Tokyo Institute of Technology, Box B-52, Nagatsuta-cho 4259, Midori-ku, Yokohama 226-8501, Japan
2. Department of Applied Chemistry, Meiji University, 1-1-1, Higashimita, Tama-ku, Kawasaki 214-8571, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00976
Reference44 articles.
1. Transition metal–catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry
2. Pd-catalyzed cross-coupling reactions of alkyl halides
3. Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
4. Secondary Alkyl Halides in Transition-Metal-Catalyzed Cross-Coupling Reactions
5. Copper‐Catalyzed Asymmetric Allylic Alkylation
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