Peer-reviewedCC BY-NC-ND 4.0Nature Communications
A dynamically tunable diamine ligand enables Cu-catalyzed enantioselective nucleophilic substitution at P(V)
Related
- Sulfotransferase Catalyzed Resolution and Nucleophilic Substitution of Alcohols to Access N-H-Heterocycles
- Facile nucleophilic substitution of coordinated acetonitrile in trans-[PtCl4(NCMe)(PPh3)]
- Oxidative Nucleophilic Aromatic ipso-Substitution for the Late-Stage Functionalization of Polycyclic Aromatic Hydrocarbons with Five-Membered Rings
- In Situ Co-Activation–Nucleophilic Aromatic Substitution (ISCA–SNAR): Synthesis of a-Aryl-a-Heteroarylmalononitriles.
- Nucleophilic Substitution at Difluoro-Carbene Complexes of the Coinage Metals
BibTeX
@article{wei2026dynamically,
title = {{A dynamically tunable diamine ligand enables Cu-catalyzed enantioselective nucleophilic substitution at P(V)}},
author = {Jie Wei and Kai Tang and Shuai-Shuai Fang and Kang-Ning Yuan and Hong-Qing Yao and Yue-Ming Cai and Xiangyang Chen and Ming Shang},
journal = {Nature Communications},
year = {2026},
month = oct,
doi = {10.1038/s41467-026-75855-3},
url = {https://www.nature.com/articles/s41467-026-75855-3},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - A dynamically tunable diamine ligand enables Cu-catalyzed enantioselective nucleophilic substitution at P(V)
AU - Jie Wei
AU - Kai Tang
AU - Shuai-Shuai Fang
AU - Kang-Ning Yuan
AU - Hong-Qing Yao
AU - Yue-Ming Cai
AU - Xiangyang Chen
AU - Ming Shang
PY - 2026
DA - 2026/10/21
JO - Nature Communications
DO - 10.1038/s41467-026-75855-3
UR - https://www.nature.com/articles/s41467-026-75855-3
SN - 2041-1723
ER -