REGIOSELECTIVE FUNCTIONALIZATION OF 1H-PYRROLO[2,3-B]PYRIDINE VIA ITS N-OXIDE

被引：0

作者：

MINAKATA, S ^{[1
]}

KOMATSU, M ^{[1
]}

OHSHIRO, Y ^{[1
]}

机构：

[1] OSAKA UNIV,FAC ENGN,DEPT APPL CHEM,SUITA,OSAKA 565,JAPAN

来源：

SYNTHESIS-STUTTGART | 1992年 / 07期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Selective functionalization of 1H-pyrrolo[2,3-b]pyridine (7-azaindole) at the 6-position was achieved by Reissert-Henze type reaction. Thus, halogeno (Cl, Br, 1), cyano and thiocyanato groups were directly introduced to the pyridine ring of 7-azaindole.

引用

页码：661 / 663

页数：3

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