Net δ-C–H Alkylation of Allyl Alcohols by Ni-Catalyzed Allylic Substitution of Azo-Ene Adducts
Transformation of allylic C-H bonds into C-C bonds in a regioselective manner represents a powerful approach to generating complex molecules from simple starting materials. Herein, we report a protocol for net δ-C-H alkylation of allyl alcohols involving a sequential azo-ene reaction and an attendant Ni-catalyzed allylic substitution with Grignard reagents. This two-step strategy enables the regioselective alkylation of distal C-H bonds, a transformation that remains challenging via direct approaches under transition-metal catalysis.
Authors
- Kiyosei Takasu (ORCID: https://orcid.org/0000-0002-1798-7919)
- Yusuke Kuroda (ORCID: https://orcid.org/0000-0003-0952-7098)
- Moe Kawajiri
Institutions
- Kyoto University (JP)
- Kyoto Pharmaceutical University (JP)
- Research Foundation ITSUU Laboratory (JP)
- Kumamoto University (JP)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-08-29
- DOI
- https://doi.org/10.1021/acs.joc.5c01497
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- Japan Agency for Medical Research and Development
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Society for the Promotion of Science