Synthesis of Isoindole Derivatives by Palladium-Catalyzed Domino Reaction of (2-Alkynyl)phenylketone O-Pentafluorobenzoyloximes

被引：18

作者：

Kitamura, Mitsuru ^{[1
]}

Moriyasu, Yohei ^{[1
]}

Okauchi, Tatsuo ^{[1
]}

机构：

[1] Kyushu Inst Technol, Dept Appl Chem, Kitakyushu, Fukuoka 8048550, Japan

来源：

SYNLETT | 2011年 / 05期

关键词：

domino reaction; isoindoles; Mizoroki-Heck reaction; oximes; palladium; HECK REACTION; ISOQUINOLINE DERIVATIVES; PYRROLE DERIVATIVES; BOND-CLEAVAGE; AMINO-HECK; CYCLIZATION; OXIMES; ARYL; 1-AZAAZULENES; AMINATION;

D O I：

10.1055/s-0030-1259556

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Isoindole derivatives were synthesized by the palladium-catalyzed cyclization of (2-alkynyl)phenylketone O-pentafluorobenzoyloximes in the presence of organometallic compounds such as sodium formate and aryl boronic acid.

引用

页码：643 / 646

页数：4

共 53 条

[1]

[Anonymous], MIZOROKIHECK REACTIO

[2] The heck reaction as a sharpening stone of palladium catalysis [J].