Synthesis of Pentacyclic Heteroaromatic Systems Related to Indolocarbazoles Alkaloids.
- 1 April 1998
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 28 (7), 1239-1251
- https://doi.org/10.1080/00397919808005966
Abstract
A direct access to pentacyclic molecules via Fischer Indole Synthesis starting from tricyclic ketones is described.Keywords
This publication has 12 references indexed in Scilit:
- SYNTHESIS OF NEW BIHETEROCYCLIC ANALOGUES OF PYRIDOCARBAZOLEShc, 1997
- Behavior of Oxotetrahydrobenzo[b]- and [c]thiophenes and Their a-Hydroxymethylene Derivatives in the Fischer Indole SynthesisHETEROCYCLES, 1996
- Preparation of thiazolocarbazoles via the Fischer indole synthesisJournal of the Chemical Society, Perkin Transactions 1, 1995
- Regioselective imide reduction : An issue in the total synthesis of staurosporineTetrahedron Letters, 1994
- Indolocarbazoles. 2. Synthetic studies towards staurosporine. An unexpected 1,2 migration of indolocarbazole nitrogen results in a novel and potent Protein kinase C inhibitor.Tetrahedron Letters, 1993
- The first synthesis of a fully functionalized core structure of staurosporine: sequential indolyl glycosidation by endo and exo glycalsJournal of the American Chemical Society, 1993
- A stereoselective synthesis of indole-.beta.-N-glycosides: an application to the synthesis of rebeccamycinThe Journal of Organic Chemistry, 1993
- Synthesis of the staurosporine aglyconThe Journal of Organic Chemistry, 1992
- Synthetic Approaches to Indolo[2,3-a]carbazole alkaloids. Syntheses of arcyriaflavin A and AT2433-B aglyconeTetrahedron, 1992
- Synthesis of the indolo[2,3-a]carbazole natural products staurosporinone and arcyriaflavin BJournal of the Chemical Society, Perkin Transactions 1, 1990