Decarbonylative Reductive Coupling of Aromatic Esters by Nickel and Palladium Catalyst

被引：5

作者：

Peng, Yunfei ^{[1
]}

Isshiki, Ryota ^{[1
]}

Muto, Kei ^{[2
]}

Yamaguchi, Junichiro ^{[1
]}

机构：

[1] Waseda Univ, Dept Appl Chem, Shinjuku Ku, 513 Wasedatsurumakicho, Tokyo 1620041, Japan

[2] Waseda Univ, Waseda Inst Adv Study, Shinjuku Ku, 513 Wasedatsurumakicho, Tokyo 1620041, Japan

来源：

CHEMISTRY LETTERS | 2022年 / 51卷 / 07期

关键词：

Decarbonylative reaction; Reductive coupling; Biaryls; ARYL BOND FORMATION; BIARYL COMPOUNDS; ALPHA-ARYLATION; C-O; PD; INTERCONVERSION; OLEFINATION; SILYLATION; CHEMISTRY; KETONES;

D O I：

10.1246/cl.220214

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Ni or Pd-catalyzed decarbonylative reductive couplings of aromatic esters were developed. A range of (hetero)aromatic esters was applicable to these reductive homocoupling reactions. Moreover, it was found that Pd-catalysis enables a reductive decarbonylative cross-coupling between two different aromatic esters to afford a nonsymmetrical biaryls system.

引用

页码：749 / 753

页数：5

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