Synthesis of Polycyclic Heteroarenes via Rh(III)-Catalyzed Twofold C-H Activation of 3-Aryl-2<i>H</i>-benzo[<i>b</i>][1,4]oxazines and Annulation with α-Diazo-β-ketoesters
An efficient Rh(III)-catalyzed annulation between 3-aryl-2<i>H</i>-benzo[<i>b</i>][1,4]oxazines and α-diazo-β-ketoesters was developed, affording a series of polycyclic heteroarenes in moderate to excellent yields with good functional group compatibility. The procedure featured high efficiency, redox neutrality, twofold <i>ortho</i>-C-H activation, and dual [4 + 2] annulation. Moreover, several important intermediates and products have been isolated as powerful evidence for the proposed reaction mechanism.
Authors
- Yiyue Li
- Xifa Yang (ORCID: https://orcid.org/0000-0002-3826-3039)
- Yi‐nan Cheng (ORCID: https://orcid.org/0000-0003-4979-1520)
- Youwu Hao (ORCID: https://orcid.org/0000-0001-7341-6371)
- Xiangyang Liu
- Li Song (ORCID: https://orcid.org/0000-0002-2724-5812)
- Haokang Du
Institutions
- Institute of Plant Protection (CN)
- Henan Agricultural University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-03-14
- DOI
- https://doi.org/10.1021/acs.joc.5c00036
- Citations
- 2
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- National Natural Science Foundation of China