Stereoselective Formation of Allyl Ethers by Reaction of Epoxides with Organic Chlorides under Liquid-Solid Phase-Transfer Catalysis
- 1 February 1987
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 60 (2) , 667-672
- https://doi.org/10.1246/bcsj.60.667
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- N-alkyl-4-(N′,N′-dialkylamino)pyridinium salts: thermally stable phase transfer catalysts for nucleophilic aromatic displacementTetrahedron Letters, 1984
- Base‐Promoted Isomerizations of EpoxidesPublished by Wiley ,1983
- Stereochemical and base species dichotomies in olefin-forming E2 eliminationsChemical Reviews, 1980
- Organosilicon compounds with functional groups proximate to silicon. Feasible route to 1,2-epoxyalkyllithium reagents via the lithiation of epoxyethylsilanesJournal of the American Chemical Society, 1976
- Base-induced rearrangement of epoxides to allylic alcohols. III. Alkylidenecycloalkane oxidesThe Journal of Organic Chemistry, 1971
- Stereochemistry of the base-induced rearrangement of epoxides to allylic alcoholsJournal of the American Chemical Society, 1970
- Stereoselectivity of the base-induced conversion of epoxides to allylic alcoholsThe Journal of Organic Chemistry, 1969
- Proximity Effects. XLII. The Reaction of Lithium Diethylamide with cis- and trans-4-Octene Oxide1Journal of the American Chemical Society, 1965
- The stereospecific ring opening rearrangement of epichlorohydrin withTetrahedron Letters, 1964
- Vinylogie chez les composés de sulfonyle I: (Propriétés du groupe sulfonyle XXXIX)Recueil des Travaux Chimiques des Pays-Bas, 1953