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.

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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

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article

Synthesis of Polycyclic Heteroarenes via Rh(III)-Catalyzed Twofold C-H Activation of 3-Aryl-2H-benzo[b][1,4]oxazines and Annulation with α-Diazo-β-ketoesters

Yiyue Li, Xifa Yang, Yi‐nan Cheng, Youwu Hao et al.
2 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
1.87
article

Synthesis of Polycyclic Heteroarenes via Rh(III)-Catalyzed Twofold C-H Activation of 3-Aryl-2H-benzo[b][1,4]oxazines and Annulation with α-Diazo-β-ketoesters

Yiyue Li, Xifa Yang, Yi‐nan Cheng, Youwu Hao, Xiangyang Liu, Li Song, Haokang Du
article en
2 citations

Abstract

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.

The Journal of Organic ChemistryVol. 90(12)
Institute of Plant Protection (CN), Henan Agricultural University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Cyclopropane Reaction Mechanisms
1.87
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