Preparation of novel aza-1,7-annulated indoles and their conversion to potent indolocarbazole kinase inhibitors
- 2 August 2004
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 14 (15) , 3925-3928
- https://doi.org/10.1016/j.bmcl.2004.05.088
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- 1,7-Annulated indolocarbazoles as cyclin-dependent kinase inhibitorsBioorganic & Medicinal Chemistry Letters, 2004
- Discovery of Antitumor Indolocarbazoles: Rebeccamycin, NSC 655649, and FluoroindolocarbazolesCurrent Medicinal Chemistry - Anti-Cancer Agents, 2002
- IndolocarhazolesPublished by Elsevier ,2001
- A new one step synthesis of maleimides by condensation of glyoxylate esters with acetamidesTetrahedron Letters, 1999
- A study on p16, pRb, cdk4 and cyclinD1 expression in non-small cell lung cancersCancer Letters, 1998
- A New, Efficient Method for the Synthesis of BisindolylmaleimidesThe Journal of Organic Chemistry, 1998
- Targets for cancer therapy in the cell cycle pathwayCurrent Opinion in Oncology, 1996
- Synthesis of 7-Formylindole Using the Bartoli Indole MethodologySynlett, 1992
- A One-Step Conversion of Certain Indole and Pyrrole Glyoxtlic Acid Esters to the Corresponding AcetatesSynthetic Communications, 1989
- The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspectsChemical Reviews, 1989