Cu/Rh-Carbene-Directed Highly Diastereoselective Dimerization of Cyclopropenes
Abstract Carbene dimerization typically proceeds through head-to-head coupling to form planar olefins. Herein we report a carbene dimerization of cyclopropenes under copper or rhodium catalysis that proceeds through sequential C–H insertion and [2 + 1] cycloaddition to furnish cyclopropa-fused indanes with excellent diastereoselectivities. The reaction features broad substrate scope, gram-scale synthesis, and versatile product transformations. Mechanistic studies and DFT calculations reveal that π–π stacking interactions govern the high diastereoselectivity.
Authors
- Xinyu Liu (ORCID: https://orcid.org/0000-0002-8010-2175)
- Nengzhong Wang (ORCID: https://orcid.org/0000-0003-1690-7611)
- Hui Qin Yao (ORCID: https://orcid.org/0000-0002-4450-8602)
- Nianyu Huang (ORCID: https://orcid.org/0000-0003-4483-160X)
- Linxuan Li (ORCID: https://orcid.org/0000-0001-9836-1442)
- Meiling Dai
- Yunfei Huang
- Lijuan Ma
Institutions
- China Three Gorges University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-10-08
- DOI
- https://doi.org/10.1021/acs.orglett.6c03719
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00