Transition Metal Complexes in Organic Synthesis, Part 70&#. Synthesis of Biologically Active Carbazole Alkaloids Using Organometallic Chemistry

Author(s): Hans-Joachim Knolker.

Journal Name: Current Organic Synthesis

Volume 1 , Issue 4 , 2004

Become EABM
Become Reviewer


The isolation and biological activity of carbazole alkaloids is summarized. Recent developments of novel methodologies for the synthesis of carbazole alkaloids are described. The focus is on syntheses using the oxidative coupling of arylamines with either arenes, cyclohexadienes, or cyclohexene mediated or catalyzed by palladium, iron, or molybdenum. The implementation of these annulations in total syntheses provides highly convergent routes to biologically active carbazole alkaloids. Advantages, scope, and limitations of the different synthetic methods are discussed.

Keywords: carbazole alkaloids, cyclohexene, cyclohexadienes, arylamines

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2004
Page: [309 - 331]
Pages: 23
DOI: 10.2174/1570179043366594
Price: $58

Article Metrics

PDF: 8