Stereoselective synthesis of the C1–C12 segment of iriomoteolide-1a: a very potent macrolide antitumor agent
- 1 April 2009
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 50 (13), 1416-1418
- https://doi.org/10.1016/j.tetlet.2009.01.043
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Synthesis of the C1−C12 Fragment of Iriomoteolide 1a by Sequential Catalytic Asymmetric Vinylogous Aldol ReactionsOrganic Letters, 2008
- Enantioselective Total Synthesis of (+)-Largazole, a Potent Inhibitor of Histone DeacetylaseOrganic Letters, 2008
- Iriomoteolide-1a, a Potent Cytotoxic 20-Membered Macrolide from a Benthic Dinoflagellate Amphidinium SpeciesThe Journal of Organic Chemistry, 2007
- Bioactive Macrolides and Polyketides from Marine Dinoflagellates of the Genus AmphidiniumJournal of Natural Products, 2007
- Macrocyclization via Allyl Transfer: Total Synthesis of LaulimalideJournal of the American Chemical Society, 2001
- Complex Target-Oriented Synthesis in the Drug Discovery Process: A Case History in the dEpoB SeriesThe Journal of Organic Chemistry, 1999
- A Stereoselective Synthesis oftrans-1,2-Disubstituted Alkenes Based on the Condensation of Aldehydes with Metallated 1-Phenyl-1H-tetrazol-5-yl SulfonesSynlett, 1998
- A chemoenzymatic synthesis of a-ring key-intermediates for 1α,25-dihydroxyvitamin d3 and analoguesTetrahedron Letters, 1995
- Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachlorideTetrahedron Letters, 1976
- .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and aminesThe Journal of Organic Chemistry, 1969