Ring opening of alkynyl sugars by Nicholas reaction—application to enantioselective synthesis of oxepane subunits of marine trans-fused polyether Toxins
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (45) , 12883-12894
- https://doi.org/10.1016/s0040-4020(01)81207-2
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Marine toxinsChemical Reviews, 1993
- Introduction of Two Glucals into Bis-SilylacetylenesSynlett, 1993
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- A mild procedure for cleavage of 1,6-anhydro sugarsJournal of the Chemical Society, Chemical Communications, 1991
- Stereoselective reaction of methyl α- and β-D-glycopyranosides with acetic anhydride in the presence of trimethylsilyl trifluoromethanesulphonateJournal of the Chemical Society, Perkin Transactions 1, 1990
- Activation of 7-endo over 6-exo epoxide openings. Synthesis of oxepane and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Dynamic behavior of dicobalt hexacarbonyl propargyl cations and their reactions with chiral nucleophilesJournal of the American Chemical Society, 1987
- Chemistry and synthetic utility of cobalt-complexed propargyl cationsAccounts of Chemical Research, 1987
- Benzyl trichloroacetimidate, a versatile reagent for acid-catalysed benzylation of hydroxy-groupsJournal of the Chemical Society, Chemical Communications, 1981
- The Molecular Configuration of Dicobalt Hexacarbonyl DiphenylacetyleneJournal of the American Chemical Society, 1959