Events The 12th International Electronic Conference on Synthetic Organic Chemistry

Event submissions

Published

This submission belongs to the session a. General Organic Synthesis of the event The 12th International Electronic Conference on Synthetic Organic Chemistry

Published date

20 Nov, 2008

Citation

Wolfgang Stadlbauer, Hoai V. Dang, Ali Deeb, Birgit Schuki, Thomas Kappe, Syntheses of 8,9,10,11-Tetrahydro-pyrido[3,2,1-jk]carbazoles, 1,2,3, 11b-Tetrahydro-pyrido[3,2,1-jk]carbazoles and 7a,8,9,10,11,11a-Hexahydro-pyrido[3,2,1-jk]carbazoles, in Proceedings of The 12th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2008, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-12-01216

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Syntheses of 8,9,10,11-Tetrahydro-pyrido[3,2,1-jk]carbazoles, 1,2,3, 11b-Tetrahydro-pyrido[3,2,1-jk]carbazoles and 7a,8,9,10,11,11a-Hexahydro-pyrido[3,2,1-jk]carbazoles

Wolfgang Stadlbauer ¹

Hoai V. Dang ¹

Ali Deeb ¹

Birgit Schuki ¹

Thomas Kappe ¹

1. Institut für Chemie, Organic Synthesis Group, Karl-Franzens-University of Graz Heinrichstrasse 28, A-8010 Graz (Austria)

Abstract

Pyrido[3,2,1-jk]carbazol-6-one in its partial hydrogenated form is part of the heterocyclic skeleton of many natural products (e. g. strychnos alkaloids such as strychninolones and brucinolones, picrasidin Q and olivacin alkaloids). It possesses the biological interesting combination of an indole structure and of a 2-quinolone; Comparison with strychnos alkaloids shows that it has already four rings and two oxygen functions in the correct position.

Keywords

n/a

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