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.
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页码：661 / 663
页数：3
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