Molybdenum-Catalyzed Reductive C–N Coupling/Cyclization Cascade for the De Novo Construction of N -Substituted Oxindoles

A simple and practical Mo-catalyzed method has been developed for the de novo and efficient synthesis of versatile N-substituted oxindoles via a reductive C-N coupling/cyclization cascade. This protocol features inexpensive starting materials, broad functional group tolerance, and is applicable to the late-stage modification or synthesis of biorelevant targets.

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Journal
The Journal of Organic Chemistry
Published
2026-11-02
DOI
https://doi.org/10.1021/acs.joc.6c02319
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
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article

Molybdenum-Catalyzed Reductive C–N Coupling/Cyclization Cascade for the De Novo Construction of N -Substituted Oxindoles

Xiaobo Xu, Xie Xiu-zhe, Zhong‐Yan Cao, Zi Yang et al.
4 links
The Journal of Organic Chemistry
Catalytic Cross-Coupling Reactions
article

Molybdenum-Catalyzed Reductive C–N Coupling/Cyclization Cascade for the De Novo Construction of N -Substituted Oxindoles

Xiaobo Xu, Xie Xiu-zhe, Zhong‐Yan Cao, Zi Yang, Weijia Wang, Shengnan Jin, Bei Ge, Chunhong Zhang, He-Han Feng
article en

Abstract

A simple and practical Mo-catalyzed method has been developed for the de novo and efficient synthesis of versatile N-substituted oxindoles via a reductive C-N coupling/cyclization cascade. This protocol features inexpensive starting materials, broad functional group tolerance, and is applicable to the late-stage modification or synthesis of biorelevant targets.

The Journal of Organic Chemistry
Changsha Medical University (CN), Nanjing Forestry University (CN), Henan University (CN), First Affiliated Hospital of Wenzhou Medical University (CN), Huanghuai University (CN)
China Postdoctoral Science Foundation, Natural Science Foundation of Henan Province, Key Scientific Research Project of Colleges and Universities in Henan Province, Science and Technology Innovation Talents in Universities of Henan Province
Openalex Percentile: Top 26%
Catalytic Cross-Coupling Reactions
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