New Regiospecific and stereoselective route to β-hydroxy selenides A (C,C) connective and stereospecific route to olefins and epoxides
Authors:
- 30 September 1976
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 17 (36) , 3227-3230
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- New regiospecific routes to olefins from β-hydroxy selenidesTetrahedron Letters, 1976
- Sur le role fondamental du cation alcalin dans la reduction par les hydrures metalliques - utilisation de coordinats macrocycliques V : La stéréodirection dans la réduction d'une cétone assujettie au modèle dipolaire.Tetrahedron Letters, 1976
- Regiospecific synthetic routes to α-seleno carbonyl compounds and to αβ-unsaturated carbonyl compoundsTetrahedron Letters, 1976
- Selenium stablized anions. Conversion of β-hydroxy selenides into olefinsJournal of the Chemical Society, Chemical Communications, 1975
- Electrophilic and nucleophilic organoselenium reagents. New routes to .alpha.,.beta.-unsaturated carbonyl compoundsJournal of the American Chemical Society, 1973
- Mild procedure for the conversion of epoxides to allylic alcohols. First organoselenium reagentJournal of the American Chemical Society, 1973
- Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketonesTetrahedron Letters, 1968
- Asymmetric Induction. A Model for Additions to Carbonyls Directly Bonded to Asymmetric CarbonsJournal of the American Chemical Society, 1967
- Studies in Stereochemistry. XXXV. Mechanism of Ei Reaction of Amine OxidesJournal of the American Chemical Society, 1963
- 24. A general stereoselective synthesis of olefinsJournal of the Chemical Society (Resumed), 1959