Synthesis of a bis-pyrrolo-quinone structure analogue to wakayin

被引:20
作者
Barret, R
Roue, N
机构
[1] Fac Pharm Lyon, Chim Therapeut Lab, F-69373 Lyon 08, France
[2] Fac Pharm, Chim Therapeut Lab, F-51100 Reims, France
关键词
D O I
10.1016/S0040-4039(99)00640-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The addition of different amines to indole-4,7-quinone is studied. The application of this reaction with indolyl-2-oxoethylamine lead to the preparation of an analogue of wakayin 2. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3889 / 3890
页数:2
相关论文
共 8 条
[1]  
Barret R, 1998, CHEM PHARM BULL, V46, P548
[2]   REGIOSELECTIVE OXIDATIVE AMINATION OF 3-CARBOMETHOXYINDOLE-4,7-QUINONES [J].
EDSTROM, ED ;
JONES, Z .
TETRAHEDRON LETTERS, 1995, 36 (39) :7039-7042
[3]   REGIOSELECTIVE AMINATION OF INDOLE-4,7-QUINONES [J].
JACKSON, YA ;
BILLIMORIA, AD ;
SADANANDAN, EV ;
CAVA, MP .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (11) :3543-3545
[4]  
KODOSHKA JM, 1996, ANTI-CANCER DRUG, V7, P758
[5]  
OIKAWA Y, 1979, HETEROCYCLES, V12, P1457
[6]  
SHOWALTER HDH, 1992, ORG PREP PROCED INT, V24, P484
[7]  
VENABLES DA, 1991, J ORG CHEM, V56, P459
[8]   Synthesis of a wakayin model compound: Oxidative formation of a new pyrrole ring in the indol-3-yl-indoloquinone system [J].
Zhang, LM ;
Cava, MP ;
Rogers, RD ;
Rogers, LM .
TETRAHEDRON LETTERS, 1998, 39 (42) :7677-7678