Chinese Journal of Organic Chemistry ›› 2026, Vol. 46 ›› Issue (7): 2723-2732.DOI: 10.6023/cjoc202603037 Previous Articles     Next Articles

ARTICLE

镍催化二肽和三肽α-C-Ts与芳基/乙烯基卤化物/三氟甲磺酸酯的非对映选择性还原偶联

安豪豪a, 胡杰b, 龚和贵a,b,*()   

  1. a 河南大学纳米科学与工程研究院 河南开封 475004
    b 上海大学理学院 超分子化学与催化研究中心 上海 200444
  • 收稿日期:2026-03-28 修回日期:2026-06-01 发布日期:2026-06-26
  • 基金资助:
    国家自然科学基金(22271182)

Ni-Catalyzed Diastereoselective Reductive Coupling of Di- and Tri-peptide α-C-Ts with Aryl/Vinyl Halides/Triflates

Haohao Ana, Jie Hub, Hegui Gonga,b,*()   

  1. a Institute of Nanoscience and Engineering, Henan University, Kaifeng, Henan 475004
    b Center for Supramolecular Chemistry and Catalysis, School of Sciences, Shanghai University, Shanghai 200444
  • Received:2026-03-28 Revised:2026-06-01 Published:2026-06-26
  • Contact: *E-mail: hegui-gong@henu.edu.cn
  • Supported by:
    National Natural Science Foundation of China(22271182)

This work highlights our continuous efforts to expand the substrate scope of the Ni-catalyzed diastereoselective reaction of peptide α-C-Ts with aryl/vinyl halides. In particular, this work is focused on efficient late-stage peptide backbone α-C-modulation with a wide range of heteroaryl halides, and the arylation of dipeptides containing the TsG unit at the C- terminals, which has not been investigated in our previous report. Thus, this study provides more interesting examples of peptides modified with α-C-aryl/vinyl groups, which could serve as useful building blocks for drug development.

Key words: arylation, vinylation, nickel, peptide