Enantioselective Synthesis of the Functionalized Bicyclo[2.2.1]heptane Derivatives, Key Intermediates for the Chiral Synthesis of Santalenes and Santalols
- 5 July 1986
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 15 (7) , 1225-1228
- https://doi.org/10.1246/cl.1986.1225
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Highly diastereoselective Diels-Alder reaction of optically active ethyl 2-p-tolylsulfinylmethylenepropionate with cyclopentadieneTetrahedron Letters, 1984
- Investigation of a chiral masked ketene synthon synthesis of the (+)-(1r4r) and (−)-1s,4s) enantiomers of dehydronorcamphorTetrahedron, 1983
- Regioselective synthesis of β-ketoesters from lithium enolates and methyl cyanoformateTetrahedron Letters, 1983
- Stereoselective Syntheses of (±)‐epi‐β‐Santalene and (±)‐epi‐β‐SantalolHelvetica Chimica Acta, 1981
- East Indian sandalwood oil. 2. Stereoselective synthesis of (.+-.)-epi-.beta.-santalene and (.+-.)-epi-.beta.-santalolThe Journal of Organic Chemistry, 1980
- Wittig-type Reaction of Dimetallated Carbodianion Species as Produced by Zinc Reduction of gem-Polyhalogen Compounds in the Presence of Lewis AcidsBulletin of the Chemical Society of Japan, 1980
- Lanthanoids in organic synthesis. 4. Selective ketalization and reduction of carbonyl groupsThe Journal of Organic Chemistry, 1979
- Oxidation of alcohols by “activated” dimethyl sulfoxide. a preparative, steric and mechanistic studyTetrahedron, 1978
- endo-Dicyclopentadiene Synthesis of (±)-Sesquifenchene and (±)-epi-β-SantaleneSynthetic Communications, 1975
- The Synthesis of d,l-β-Santalene and d,l-epi-β-Santalene by Stereospecific RoutesJournal of the American Chemical Society, 1962