镍催化芳香羧酸与P(O)-H(2)化合物脱羰基化形成C-P键

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Jia-Xin Li, Rui Tian and Yong-Ming Zhu*, 
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引用次数: 0

摘要

开发了一种新的碳-磷键形成策略。该反应以芳香族羧酸为芳香族基团来源,无需分离中间体即可与三种P(O)-H(2)化合物偶联,从而实现了碳磷键的一锅式构建。该方案具有优异的适用性和功能基团耐受性,能够以中等至优异的收率生产Ar-P (O)R2和Ar2-PPh。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nickel-Catalyzed Decarbonylation of Aromatic Carboxylic Acids with P(O)-H(2) Compounds to Form C–P Bonds

Nickel-Catalyzed Decarbonylation of Aromatic Carboxylic Acids with P(O)-H(2) Compounds to Form C–P Bonds

A novel strategy for C–P bond formation has been developed. The reaction employed aromatic carboxylic acids as the source of aromatic groups to couple with three types of P(O)-H(2) compounds without the need to isolate intermediates, thereby achieving a one-pot construction of carbon–phosphorus bonds. The protocol demonstrated excellent applicability and functional group tolerance, enabling the production of Ar–P(O)R2 and Ar2–PPh with moderate to excellent yields.

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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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