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
    EDSTROM, ED
    JONES, Z
    [J]. TETRAHEDRON LETTERS, 1995, 36 (39) : 7039 - 7042
  • [3] REGIOSELECTIVE AMINATION OF INDOLE-4,7-QUINONES
    JACKSON, YA
    BILLIMORIA, AD
    SADANANDAN, EV
    CAVA, MP
    [J]. 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
    Zhang, LM
    Cava, MP
    Rogers, RD
    Rogers, LM
    [J]. TETRAHEDRON LETTERS, 1998, 39 (42) : 7677 - 7678