Forging 1,1′-Bicyclopropenyls by Synergistic Au/Ag Dual-Catalyzed Cyclopropenyl Cross-Coupling
1,1'-Bicyclopropenyl is a constitutional isomer of benzene comprising two coupled cyclopropene units with the endocyclic double bonds in conjugation. Due to the intrinsic high strain energy, it remains a long-standing challenge to prepare 1,1'-bicyclopropenyl derivatives, particularly multisubstituted, nonsymmetrical ones, in an efficient and modular manner. Herein a straightforward Au/Ag bimetallic-catalyzed cyclopropenyl cross-coupling has been developed, providing a robust and versatile strategy for the rapid assembly of symmetrical and unsymmetrical 1,1'-bicyclopropenyl derivatives from cyclopropenyl benziodoxoles (CpBXs) and terminal cyclopropenes. Advantages of this strategy include tolerance to a wide range of synthetically useful functional groups, mild reaction conditions, and a simple catalytic system. The obtained 1,1'-bicyclopropenyl derivatives were shown to be valuable synthetic intermediates through selective downstream manipulations.
Authors
- Jérôme Waser (ORCID: https://orcid.org/0000-0002-4570-914X)
- Xiangdong Li (ORCID: https://orcid.org/0000-0003-1448-052X)
Institutions
- Institute of Organic Synthesis (RU)
- Laboratoire de Synthèse Organique (FR)
- Chemical Synthesis Lab (SG)
- École Polytechnique Fédérale de Lausanne (CH)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2024-10-18
- DOI
- https://doi.org/10.1021/jacs.4c10996
- Citations
- 14
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 3.50
Funders
- École Polytechnique Fédérale de Lausanne