Stereocontrolled synthesis of key intermediates in the total synthesis of acetogenins of annonaceae
- 10 December 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (50), 8093-8096
- https://doi.org/10.1016/s0040-4039(00)61460-0
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Bis-tetrahydrofuran acetogenins from annonaceaePhytochemistry, 1993
- Synthetic routes to 2,5-disubstituted tetrahydrofuransTetrahedron: Asymmetry, 1993
- Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxideThe Journal of Organic Chemistry, 1993
- Total synthesis of naturally occurring acetogenins: solamin and reticulatacinJournal of the American Chemical Society, 1993
- Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivativesJournal of the American Chemical Society, 1992
- Molecular mode of action of annoninsPesticide Science, 1991
- Solamin, a cytotoxic mono-tetrahydrofuranic γ-lactone acetogenin from Annona muricata seedsPhytochemistry, 1991
- The four-carbon elongation of aldehydo sugars using 2-(trimethylsiloxy)furan: a butenolide route to higher monosaccharidesThe Journal of Organic Chemistry, 1990
- Annonaceous Acetogenins: A ReviewJournal of Natural Products, 1990
- Diastereoselectivity in the directed aldol condensation of 2-trimethylsiloxyfuran with aldehydes. A stereodivergent route to threo and erythro δ-hydroxy-γ-lactonesTetrahedron Letters, 1987