[Synthesis of carbazole derivatives. 1. The reaction of 3-(2-nitroethenyl)-indole-2-malonic acid esters with Michael acceptors].

Abstract:

:Michael-type reaction of compounds of type 9 were studied. Addition reactions with acrolein and methyl vinyl ketone, respectively, lead--depending on the conditions--to pyridoindoles of type 16 and 14 and/or to tetrahydrocarbazoles of type 17 and 15. With Triton B compounds 15 undergo retro-Michael-type elimination of the nitromethyl group, followed by hydrolysis/decarboxylation and dehydrogenation, leading to the disubstituted carbazoles 20. In the case of 17a, the primary elimination product 18 could be isolated. The synthetic potential of these reaction types is discussed. Some of the described compounds and derivatives of them show antimycobacterial activity.

journal_name

Arch Pharm (Weinheim)

journal_title

Archiv der Pharmazie

authors

Mahboobi S,Burgemeister T,Kastner F

doi

10.1002/ardp.19953280107

subject

Has Abstract

pub_date

1995-01-01 00:00:00

pages

29-38

issue

1

eissn

0365-6233

issn

1521-4184

journal_volume

328

pub_type

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