Novel stereoselective construction of a quaternary carbon: application to synthesis of the cyclopentenedione moiety of madindolines
- 1 August 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (33) , 6429-6433
- https://doi.org/10.1016/s0040-4039(00)00937-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Total Synthesis of (+)-Madindoline A and (−)-Madindoline B, Potent, Selective Inhibitors of Interleukin 6. Determination of the Relative and Absolute ConfigurationsJournal of the American Chemical Society, 2000
- Alkylation of lithium dienediolates of butenoic acids. Regioselectivity effects of structure and leaving group of the alkylating agentTetrahedron, 1998
- The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon StereocentersAngewandte Chemie International Edition in English, 1998
- Madindolines, Novel Inhibitors of IL-6 Activity from Streptomyces sp. K93-0711. II. Physico-chemical Properties and Structural Elucidation.The Journal of Antibiotics, 1997
- Madindoline, a Novel Inhibitor of IL-6 Activity from Streptomyces sp. K93-0711. I. Taxonomy, Fermentation, Isolation and Biological Activities.The Journal of Antibiotics, 1996
- Asymmetric creation of quaternary carbon centersChemical Reviews, 1993
- Organic reactions at high pressure. Conversion of cyclic alkanones and enones to 1,3-dioxolanesThe Journal of Organic Chemistry, 1986
- Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivativesJournal of the American Chemical Society, 1982
- Activated Dimethyl Sulfoxide: Useful Reagents for SynthesisSynthesis, 1981
- Reactions de transcetalisation—IITetrahedron, 1978