An easy approach to chiral non-racemic 6-(furan-3-yl)-5,6-dihydro-pyran-2-ones
- 1 July 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (13) , 2197-2199
- https://doi.org/10.1016/s0957-4166(98)00210-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Stereoselective approach to the BCD framework of richardianidins via intramolecular reformatsky-type reaction promoted by diethylaluminum chlorideTetrahedron Letters, 1997
- A new approach to pyranofuranones, advanced intermediates for the synthesis of manoalide, cacospongionolides and their analoguesTetrahedron Letters, 1996
- Cacospongionolide B, a New Sesterterpene from the Sponge Fasciospongia cavernosaJournal of Natural Products, 1995
- An Efficient Asymmetric Aldol Reaction of 4-Trimethylsiloxy-6-methylene-1,3-dioxines by Chiral Binaphthol-Titanium Complex CatalysisHETEROCYCLES, 1995
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- 1,3- diastereoselective reduction of β-hydroxyketones utilizing alkoxydialkylboranesTetrahedron Letters, 1987
- Manoalide, an antibiotic sesterterpenoid from the marine sponge (polejaeff)Tetrahedron Letters, 1980
- ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogensis produced by Penicillium citrinum.The Journal of Antibiotics, 1976