Rhodium-Catalyzed Enantio- and Diastereoselective Synthesis of Allenyl Alcohols via Three-Component Dicarbofunctionalization of 1,3-Enynes
Multicomponent reactions have the advantage of high step-economy with the formation of multiple bonds in a controlled manner in a single operation. Nevertheless, asymmetric C–H bond activation that enables three-component coupling remains largely underexplored. Reported herein is rhodium-catalyzed C–H bond activation of indoles and sequential addition to 1,3-enyne and an activated aldehyde, allowing facile synthesis of chiral allenyl alcohols in high regio-, enantio-, and diastereoselectivity under mild reaction conditions. Mechanistic studies suggested the involvement of C–H bond activation and olefin insertion that gives a rhodium(III) propargyl intermediate, and the interaction between the propargyl and the aldehyde is both enantio- and diastereo-determining. In particular, a silver additive serves to enhance the diastereoselectivity.
Authors
- Heng Song (ORCID: https://orcid.org/0000-0002-2340-1208)
- Ruijie Mi (ORCID: https://orcid.org/0009-0005-9249-6641)
- Xingwei Li (ORCID: https://orcid.org/0000-0002-1153-1558)
Institutions
- Shandong University (CN)
- Shaanxi Normal University (CN)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2025-08-20
- DOI
- https://doi.org/10.1021/acscatal.5c05041
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Natural Science Foundation of China
- National Key Research and Development Program of China