Recent advances in photocatalytic C-H amination to nitrogenous structures

Nitrogen-containing structures represent a significant branch exhibiting remarkable biological activity, surpassing non-nitrogen architectures. Given the vast array of nitrogen-containing compounds and their crucial role in the pharmaceutical industry, chemists have been motivated to devise efficient, cost-effective, and practical methods for C-N bond formation. Significant advancements have been achieved in this cutting-edge field over the past few decades. This review aims to encapsulate the latest progress in C-N bond formation via the photocatalytic C-H amination process. Initially, we provide a comprehensive introduction to C-H amination transformations. Subsequently, we categorize these photochemical conversions into two parts: intramolecular and intermolecular C-H amination. To elucidate the underlying principles of specific illustrative examples, we have carefully chosen and elaborated on the reaction mechanisms, representative experimental outcomes, and applications. Nitrogen-containing structures represent a significant branch exhibiting remarkable biological activity, surpassing non-nitrogen architectures. The review is organized into sections based on the various photo-induced catalytic systems employed. Within each section, we delve into the specific reaction conditions, the range of substrates used, and the underlying reaction mechanisms involved in photochemical C-H amination transformations.

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Publication Details

Journal
Green Synthesis and Catalysis
Published
2024-10-05
DOI
https://doi.org/10.1016/j.gresc.2024.09.010
Citations
7
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
1.75

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article

Recent advances in photocatalytic C-H amination to nitrogenous structures

Yuyo Go, Yuanyuan Chang, Linlin Shi, Bingjie Li et al.
7 citations
Green Synthesis and Catalysis
Synthesis and Catalytic Reactions
1.75
article

Recent advances in photocatalytic C-H amination to nitrogenous structures

Yuyo Go, Yuanyuan Chang, Linlin Shi, Bingjie Li, Lu Chen, Bin Wang, J.‐M. Yang, Di Wu, Chunzheng Ma
article en
7 citations

Abstract

Nitrogen-containing structures represent a significant branch exhibiting remarkable biological activity, surpassing non-nitrogen architectures. Given the vast array of nitrogen-containing compounds and their crucial role in the pharmaceutical industry, chemists have been motivated to devise efficient, cost-effective, and practical methods for C-N bond formation. Significant advancements have been achieved in this cutting-edge field over the past few decades. This review aims to encapsulate the latest progress in C-N bond formation via the photocatalytic C-H amination process. Initially, we provide a comprehensive introduction to C-H amination transformations. Subsequently, we categorize these photochemical conversions into two parts: intramolecular and intermolecular C-H amination. To elucidate the underlying principles of specific illustrative examples, we have carefully chosen and elaborated on the reaction mechanisms, representative experimental outcomes, and applications. Nitrogen-containing structures represent a significant branch exhibiting remarkable biological activity, surpassing non-nitrogen architectures. The review is organized into sections based on the various photo-induced catalytic systems employed. Within each section, we delve into the specific reaction conditions, the range of substrates used, and the underlying reaction mechanisms involved in photochemical C-H amination transformations.

Green Synthesis and CatalysisVol. 7(1)
Henan University of Traditional Chinese Medicine (CN), Shantou University (CN), Zhengzhou University (CN), University of Oxford (GB), First Affiliated Hospital of Shantou University Medical College (CN), First Affiliated Hospital of Zhengzhou University (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Natural Science Foundation of Henan Province
Openalex Percentile: Top 16%
Synthesis and Catalytic Reactions
1.75
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