Rhodium(III)-catalyzed Oxidative Coupling through C-H Bond Cleavage Directed by Phosphinoxy Groups

被引：124

作者：

Unoh, Yuto ^{[1
]}

Hashimoto, Yuto ^{[1
]}

Takeda, Daisuke ^{[1
]}

Hirano, Koji ^{[1
]}

Satoh, Tetsuya ^{[1
,2
]}

Miura, Masahiro ^{[1
]}

机构：

[1] Osaka Univ, Fac Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan

[2] JST, ACT C, Kawaguchi, Saitama 3320012, Japan

来源：

ORGANIC LETTERS | 2013年 / 15卷 / 13期

关键词：

CATALYZED ANNULATION; INTERNAL ALKYNES; BENZOIC-ACIDS; PHOSPHAISOCOUMARINS; DERIVATIVES; COUPLING/CYCLIZATION; FUNCTIONALIZATION; ACTIVATION; BENZAMIDES; CARBON;

D O I：

10.1021/ol4012794

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A straightforward synthesis of phosphaisocoumarins is achieved by the rhodium-catalyzed oxidative coupling of diarylphosphinic and phenylphosphonic acid derivatives with alkynes. The P-OH groups effectively act as the key function for the regioselective C-H bond cleavage. Related oxidative coupling of phenylphosphine oxides with alkenes can also be conducted smoothly under similar conditions.

引用

页码：3258 / 3261

页数：4

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