Photo-Induced Aliphatic C–H Amination Mediated by Hydrogen Atom Transfer of an Alkoxycarbonyloxyl Radical and Its Utilization for Diastereoselective Modification of Proline Residues in Peptides

)-H sites. By employing proline-containing C-H substrates, the protocol is amenable to precise manipulation of peptide skeletons through a diastereoselective process.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-01
DOI
https://doi.org/10.1021/jacs.6c03204
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Photo-Induced Aliphatic C–H Amination Mediated by Hydrogen Atom Transfer of an Alkoxycarbonyloxyl Radical and Its Utilization for Diastereoselective Modification of Proline Residues in Peptides

Dandan Yuan, Lihong Hu, Hongdie Zhang, Yangpeng Shen et al.
Journal of the American Chemical Society
Radical Photochemical Reactions
article

Photo-Induced Aliphatic C–H Amination Mediated by Hydrogen Atom Transfer of an Alkoxycarbonyloxyl Radical and Its Utilization for Diastereoselective Modification of Proline Residues in Peptides

Dandan Yuan, Lihong Hu, Hongdie Zhang, Yangpeng Shen, Jianming Yan, Jiali Cao, Yiqing Huang, Anqi Ding, Can Lu, Yujian Mao, Bohan Li, Fei Xue, Longyuan Zheng
article en

Abstract

)-H sites. By employing proline-containing C-H substrates, the protocol is amenable to precise manipulation of peptide skeletons through a diastereoselective process.

Journal of the American Chemical SocietyVol. 148(14)
Nanjing University of Chinese Medicine (CN), Nanjing Forestry University (CN)
Chongqing Medical University, Natural Science Foundation of Jiangsu Province, Jiangsu Provincial Department of Education, Nanjing University of Chinese Medicine
Affordable and clean energy
Openalex Percentile: Top 31%
Radical Photochemical Reactions
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