High diastereofacial selectivity in the reaction of silyl enol ethers with chlorosulfides
- 1 October 1991
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 47 (41), 8753-8766
- https://doi.org/10.1016/s0040-4020(01)96197-6
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Mechanistic insight into allylmetal-thioacetal reactions employing 2-acetoxy-2-phenylacetaldehyde thioacetalsThe Journal of Organic Chemistry, 1990
- An Efficient Regio and Stereoselective Synthesis of Silyl Enol EthersSynthetic Communications, 1988
- Synthetic Applications of Double Functionalization by Cooperating Sulfur- and Oxygen-Containing SubstituentsSynthesis, 1988
- High diastereofacial selectivity in nucleophilic additions to chiral thionium ionsJournal of the American Chemical Society, 1987
- An Efficient and Convenient Method for the Asymmetric Allylation of Aldehydes with Allyltrimethylsilane Catalyzed by Diphenylboryl TriflateChemistry Letters, 1987
- A new acylation catalystJournal of the Chemical Society, Chemical Communications, 1987
- Asymmetric synthesis via acetal templates. 13. Preparation of aldol compounds from butane-1,3-diol acetalsThe Journal of Organic Chemistry, 1987
- A CONVENIENT METHOD FOR THE PREPARATION OF γ-KETOSULFIDES FROM THIOACETALSChemistry Letters, 1985
- Generation of carbon-carbon double bonds from .beta.-oxygenated phenylseleno, phenylthio, and iodo species. A new use for the chlorotrimethylsilane-sodium iodide reagentThe Journal of Organic Chemistry, 1981
- Umpolung of the Reactivity of Carbonyl Compounds Through Sulfur-Containing ReagentsSynthesis, 1977