Chelation-controlled stereospecific ring-opening arylation of α-aminoaryl-tethered alkylidenecyclopropanes: stereoselective synthesis of polysubstituted conjugated dienes
A palladium-catalyzed stereospecific ring-opening arylation of α-aminoaryl-tethered alkylidenecyclopropanes for the stereoselective synthesis of 1,1,2-trisubstituted conjugated dienes has been developed.
Authors
- Ying Tang (ORCID: https://orcid.org/0000-0001-7515-3552)
- Yong-Yu He
- W. LUO (ORCID: https://orcid.org/0009-0008-3201-2387)
- Ai‐Jun Ma (ORCID: https://orcid.org/0000-0001-7757-0800)
- Jin‐Bao Peng (ORCID: https://orcid.org/0000-0002-0568-7740)
- Miao-Miao Ji
Institutions
- Wuyi University (CN)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5qo00496a
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Wuyi University
- Department of Education of Guangdong Province