AZIDE-CATALYZED REARRANGEMENT OF N-(ARYLOXY)PYRIDINIUM SALTS - FACILE SYNTHESIS OF 3-(O-HYDROXYPHENYL)PYRIDINES

被引：6

作者：

ABRAMOVITCH, RA ^{[1
]}

MILLER, AL ^{[1
]}

RADZIKOWSKA, TA ^{[1
]}

TOMASIK, P ^{[1
]}

机构：

[1] PEDAGOGICAL UNIV, PL-42201 CZESTOCHOWA, POLAND

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 03期

关键词：

D O I：

10.1021/jo01317a040

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

N-(Aryloxy)pyridinium tetrafluoroborates react with azide (and other) ions in solution to give good yields of 3-(o-hydroxyphenyl)pyridines under mild conditions; the rearrangements may be rationalized by invoking either a 3, 5 shift or a homolysis and radical recombination. © 1979, American Chemical Society. All rights reserved.

引用

页码：464 / 465

页数：2