Practical synthesis of optically pure 3,4-epoxy-5-methyldihydro-2(3H)-furanones from d-xylose by regio- and stereo-selective functionalization
- 1 August 1991
- journal article
- Published by Elsevier in Carbohydrate Research
- Vol. 214 (1) , 87-93
- https://doi.org/10.1016/s0008-6215(00)90532-9
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Stereocontrolled synthesis of (3,4,5)-3-alkyl-4-hydroxy-5-methyl-2(3)-dihydrofubanones and derivativesTetrahedron, 1988
- Enantiomeric β-angelica lactone epoxides: their syntheses from suitable chiral precursors and their use in the preparation of blastmycinoneTetrahedron, 1987
- β‐Angelica lactone epoxide: Chemical behaviour and some synthetic applicationsJournal of Heterocyclic Chemistry, 1987
- Highly stereo and regiocontrolled synthesis of both racemic and optically active (−)-blastmycinoneTetrahedron Letters, 1985
- Use of D-ribonolactone in organic synthesis. 2. Scope and utilityThe Journal of Organic Chemistry, 1984
- γ-Lactones from Mezilaurus synandraPhytochemistry, 1983
- Stereoselektive Synthese enantiomerenreiner Naturstoffe — Beispiel ÖstronAngewandte Chemie, 1983
- Lipid and terpenoid metabolites of the Gorgonian Plexaura flavaAustralian Journal of Chemistry, 1982
- Syntheses of (+) and (-) tetrahydrocerulenin from D-xylose revised stereochemistry of natural (+) ceruleninTetrahedron Letters, 1978
- Puromycin. Synthetic Studies. XIII. Synthesis of 6-Dimethylamino-9-(3'-amino-3'-deoxy-β-D-arabinofuranosyl)- purineJournal of the American Chemical Society, 1955