Access to a Welwitindolinone Core Using Sequential Cycloadditions
- 16 July 2009
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 11 (16), 3782-3785
- https://doi.org/10.1021/ol901499b
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Concise Synthesis of the Bicyclic Scaffold of N-Methylwelwitindolinone C Isothiocyanate via an Indolyne CyclizationOrganic Letters, 2009
- Asymmetric Synthesis of Bicyclo[4.3.1]decadienes and Bicyclo[3.3.2]decadienes via [6 + 3] Trimethylenemethane Cycloaddition with TroponesJournal of the American Chemical Society, 2008
- Enantioselective Construction of Spirocyclic Oxindolic Cyclopentanes by Palladium-Catalyzed Trimethylenemethane-[3+2]-CycloadditionJournal of the American Chemical Society, 2007
- Palladium-Catalyzed Asymmetric [3 + 2] Trimethylenemethane Cycloaddition ReactionsJournal of the American Chemical Society, 2006
- Rhodium(I)-Catalyzed Nucleophilic Ring-Opening Reactions of Oxabicyclo Adducts Derived from the [4 + 2]-Cycloaddition of 2-Imido-Substituted FuransThe Journal of Organic Chemistry, 2006
- Total Synthesis of (±)-Welwitindolinone A IsonitrileJournal of the American Chemical Society, 2006
- Enantioselective Total Syntheses of Welwitindolinone A and Fischerindoles I and GJournal of the American Chemical Society, 2005
- Intramolecular Amidofuran Cycloadditions across an Indole π-Bond: An Efficient Approach to theAspidospermaandStrychnosABCECoreOrganic Letters, 2002
- Oxidized Welwitindolinones from Terrestrial Fischerella spp.Journal of Natural Products, 1999
- Microtubule effects of welwistatin, a cyanobacterial indolinone that circumvents multiple drug resistance.1996