Nickel-Catalyzed Nucleophilic Substitution of Cyclopropenes by Secondary Phosphines

Abstract Research on the efficient synthesis of allylphosphine compounds is of crucial significance. Herein, a nickel-catalyzed ring-opening of cyclopropenes is described to synthesize allylphosphine compounds. This transformation enables a mild and efficient preparation of allylphosphine compounds in good yields, with 100% atom efficiency.

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Publication Details

Journal
Synlett
Published
2025-04-09
DOI
https://doi.org/10.1055/a-2579-3319
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Nickel-Catalyzed Nucleophilic Substitution of Cyclopropenes by Secondary Phosphines

Yicong Qi, Haisheng Fang, Liyan Yuwen, Qing‐Wei Zhang et al.
Synlett
Cyclopropane Reaction Mechanisms
article

Nickel-Catalyzed Nucleophilic Substitution of Cyclopropenes by Secondary Phosphines

Yicong Qi, Haisheng Fang, Liyan Yuwen, Qing‐Wei Zhang, Jingwen Wang
article en

Abstract

Abstract Research on the efficient synthesis of allylphosphine compounds is of crucial significance. Herein, a nickel-catalyzed ring-opening of cyclopropenes is described to synthesize allylphosphine compounds. This transformation enables a mild and efficient preparation of allylphosphine compounds in good yields, with 100% atom efficiency.

SynlettVol. 36(12)
University of Science and Technology of China (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 95%
Cyclopropane Reaction Mechanisms
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Nickel-Catalyzed Nucleophilic Substitution of Cyclopropenes by Secondary Phosphines — Yicong Qi, Haisheng Fang, et al. · Synlett (2025) | TGRS Research Map | TGRS