An unexpected rearrangement of 3-unsubstituted-2-acyl substituted indole phenylhydrazones.: A new method for benz[c]β-carboline synthesis

被引:6
作者
Baranova, OV [1 ]
Dubovitskii, SV [1 ]
机构
[1] Far Eastern State Univ, Dept Chem, Vladivostok 690950, Russia
关键词
Fischer's rearrangement; phenylhydrazones; rearrangement; beta-carbolines;
D O I
10.1016/j.tetlet.2003.11.059
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new type of rearrangement of 3-unsubstituted-2-acyl substituted indole phenylhydrazones with formation of a quinoline ring under acid catalysed conditions was observed. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1299 / 1300
页数:2
相关论文
共 3 条
[1]   Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C. [J].
Dubovitskii, SV .
TETRAHEDRON LETTERS, 1996, 37 (29) :5207-5208
[2]   TOTAL SYNTHESES OF THE MARINE SPONGE PIGMENTS FASCAPLYSIN AND HOMOFASCAPLYSIN-B AND HOMOFASCAPLYSIN-C [J].
GRIBBLE, GW ;
PELCMAN, B .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (13) :3636-3642
[3]   PARA-TOLUENESULFONIC ACID AND CATION-EXCHANGE RESIN IN APROTIC-SOLVENT - VALUABLE CATALYSTS FOR FISCHER INDOLIZATION [J].
MURAKAMI, Y ;
YOKOYAMA, Y ;
MIURA, T ;
HIRASAWA, H ;
KAMIMURA, Y ;
IZAKI, M .
HETEROCYCLES, 1984, 22 (05) :1211-1216