1,1-Carboamination of Terminal Alkenes via a Reaction of Azo-Ene Adducts with Grignard Reagents
Author:
Affiliation:
1. Research Foundation ITSUU Laboratory, C1232 Kanagawa Science Park R&D Building, 3-2-1 Sakado, Takatsu-ku, Kawasaki, Kanagawa 213-0012, Japan
2. Graduate School of Pharmaceutical Sciences, Kyoto University Yoshida, Sakyo-ku, Kyoto 606-8501, Japan
Funder
Ministry of Education, Culture, Sports, Science and Technology
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.2c02585
Reference37 articles.
1. Making carbon-nitrogen bonds in biological and chemical synthesis
2. Statistical Investigation into the Structural Complementarity of Natural Products and Synthetic Compounds
3. Chiral Amine Synthesis
4. Hydroamination, Aminoboration, and Carboamination with Electrophilic Amination Reagents: Umpolung-Enabled Regio- and Stereoselective Synthesis of N-Containing Molecules from Alkenes and Alkynes
5. Transition Metal‐Catalyzed Carboamination of Alkenes and Allenes: Recent Progress
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