Nickel-Catalyzed, Copper-Assisted Aromatic C–H Phosphinylation of [2.2]Paracyclophanes via Arylsulfonium Salts

-[2.2]paracyclophanylated products in good to excellent yields. The applicability of the present protocol was established through scalable preparation of the typical target product and its application as a potentially useful phosphine ligand for transition-metal-catalyzed carbene insertion to X-H (X = C, N) bonds.

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Publication Details

Journal
Organic Letters
Published
2026-06-09
DOI
https://doi.org/10.1021/acs.orglett.6c02112
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Nickel-Catalyzed, Copper-Assisted Aromatic C–H Phosphinylation of [2.2]Paracyclophanes via Arylsulfonium Salts

Liandi Wang, Kaikai Wu, Mingrui Li, Ping Wu et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Nickel-Catalyzed, Copper-Assisted Aromatic C–H Phosphinylation of [2.2]Paracyclophanes via Arylsulfonium Salts

Liandi Wang, Kaikai Wu, Mingrui Li, Ping Wu, Zhengkun Yu, Yong‐Gui Zhou, Kaiyuan Yang
article en

Abstract

-[2.2]paracyclophanylated products in good to excellent yields. The applicability of the present protocol was established through scalable preparation of the typical target product and its application as a potentially useful phosphine ligand for transition-metal-catalyzed carbene insertion to X-H (X = C, N) bonds.

Organic Letters
University of Science and Technology of China (CN), Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
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Nickel-Catalyzed, Copper-Assisted Aromatic C–H Phosphinylation of [2.2]Paracyclophanes via Arylsulfonium Salts — Liandi Wang, Kaikai Wu, et al. · Organic Letters (2026) | TGRS Research Map | TGRS