Diastereoselective synthesis of 2,3-disubstituted tetrahydrofuran synthons via the iodoetherification reaction. A transition state model based rationalization of the allylic asymmetric induction
- 1 March 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (6) , 2204-2210
- https://doi.org/10.1021/ja00188a039
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Stereoselective intramolecular iodoetherification of 4-pentene-1,3-diols: synthesis of cis-2-(iodomethyl)-3-hydroxytetrahydrofuransThe Journal of Organic Chemistry, 1987
- Conformational populations and reaction ratesThe Journal of Organic Chemistry, 1986
- Electrophile-mediated cyclizations of 6-O-benzyl-1,2-di- deoxy-3,4-O-isopropylidene-d-ribo-hex-1-enitol to derivatives of 2,5-anhydro-6-O-benzyl-3,4-O-isopropylidene-d-altro-hexitolCarbohydrate Research, 1985
- A totally synthetic route to lincosamine: some observations on the diastereofacial selectivity of electrophilic reactions on the double bonds of various 5-(1-alkenyl)arabinopyranosidesJournal of the American Chemical Society, 1985
- Diastereoselective benzyloxymercuration/demercuration of derivatives of .gamma.-alkyl-.delta.-hydroxy-.alpha.,.beta.-unsaturated esters. A new strategy for the synthesis of aldol-type productsJournal of the American Chemical Society, 1983
- Total synthesis of Lauraceae lactones: obtusilactones, litsenolides, and mahubanolidesJournal of the American Chemical Society, 1981