Access to (bridged) bicyclic ureas through azocarboxamide-enabled enantioselective 1,2-diamination of α-branched cyclic ketones
Reported here is the azocarboxamide-enabled enantioselective 1,2-diamination of α-branched cyclic ketones. A wide range of fused and bridged bicyclic ureas were prepared in good yield with excellent enantioselectivity.
Authors
- Guang‐Jian Mei (ORCID: https://orcid.org/0000-0002-8248-2327)
- Linlin Shi (ORCID: https://orcid.org/0000-0001-9089-2388)
- Yuan-Yang Li (ORCID: https://orcid.org/0009-0007-1294-8447)
- Beiling Gao (ORCID: https://orcid.org/0009-0000-2904-1349)
- Li Li (ORCID: https://orcid.org/0000-0001-6746-4297)
- Beibei Li (ORCID: https://orcid.org/0000-0002-7173-5894)
Institutions
- Zhengzhou University (CN)
- Jiaozuo University (CN)
Publication Details
- Journal
- Organic Chemistry Frontiers
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d4qo02318h
- Citations
- 3
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 1.61