Synthesis of 2,3′-diindolylmethanes and substituted indolo[3,2-b]carbazoles

被引：23

作者：

Wahlström, N

Stensland, B

Bergman, J ^{[1
]}

机构：

[1] Karolinska Inst, Biosci NOVUM, Dept Organ Chem, S-14157 Huddinge, Sweden

[2] Sodertorn Univ Coll, S-14104 Huddinge, Sweden

[3] Astrazenca PAR&D, Solid State Anal SBBG, S-15185 Sodertalje, Sweden

来源：

SYNTHESIS-STUTTGART | 2004年 / 08期

关键词：

bisindoles; acylations; Lewis acids; aryl hydrocarbon receptor; indolo[3,2-b]carbazole;

D O I：

10.1055/s-2004-822347

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Three different synthetic routes to substituted 2,3'-diindolylmethanes, and the syntheses of substituted indolo[3,2-b]carbazoles are described. The first rigid proof of an acylation in the 2-position of a 1,3-unsubstituted indole is also presented in the form of an X-ray structure.

引用

收藏

页码：1187 / 1194

页数：8

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