Synthesis of indoles and quinolones by sequential Wittig and Heck reactions

被引：36

作者：

Latham, EJ ^{[1
]}

Stanforth, SP ^{[1
]}

机构：

[1] NORTHUMBRIA UNIV,DEPT CHEM & LIFE SCI,NEWCASTLE TYNE NE1 8ST,TYNE & WEAR,ENGLAND

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1997年 / 14期

关键词：

D O I：

10.1039/a701282i

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Trifluoroacetamido derivatives 18a-c and 19a-c react with phosphorane 2 in-boiling toluene to give the corresponding enamines 12a-c and 13a-c respectively which are precursors of the trifluoromethylated indoles 14a-c and quinolones 15a-c.

引用

页码：2059 / 2063

页数：5

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