Substrate-controlled mechanistic switch between protodemetalation and oxidative addition in Rh-catalyzed carbometalation: a DFT study
Abstract
This DFT study reveals substrate-dependent mechanisms in Rh( i )-catalyzed carbometalation: dihydropyridines undergo insertion/protodemetalation, while dihydroquinolines favor oxidative addition, dictating enantioselectivity at different steps.
Fields of Study & Subjects
Organometallic Complex Synthesis and Catalysis
Cyclopropane Reaction Mechanisms
Asymmetric Synthesis and Catalysis
Publication details
- Journal / source
- Organic Chemistry Frontiers
- Volume
- 13
- Issue
- 5
- Pages
- 1657–1666
- Publication date
- 1 January 2026
- Language
- EN