The synthesis of angular methyl substituted bicyclic enones via a unique regioselective enamine annulation reaction
- 1 January 1976
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 32 (12) , 1415-1421
- https://doi.org/10.1016/0040-4020(76)85022-3
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Convenient stereospecific synthesis of(+)-.alpha.-cyperoneThe Journal of Organic Chemistry, 1974
- The conversion of 2,x-disubstituted cyclohexanones to their less stable isomers—the stereochemical implications of enamine hydrolysisTetrahedron, 1974
- Pentacyclic Triterpene Synthesis. IV a New Method for Accomplishing Robinson-Nazarov AnnelationsSynthetic Communications, 1974
- Zur Kenntnis der sesquiterpenoiden C12‐Ketone des ätherischen Öls von Vetiveria zizanioides (L.) NashHelvetica Chimica Acta, 1972
- Reactions involving electron transfer. II. Reductions of enones with alkali metal solutionsJournal of the American Chemical Society, 1970
- Synthesis and properties of 1H-naphtho[2,1-b]thiete 2,2-dioxideThe Journal of Organic Chemistry, 1968
- Enamines. II. Factors determining the structure of enamines of 2-substituted ketonesThe Journal of Organic Chemistry, 1967
- Structure and Absolute Configuration of ValeranoneCHEMICAL & PHARMACEUTICAL BULLETIN, 1965
- The structure of enamines of 2-substituted ketonesTetrahedron Letters, 1965
- The structure of cyperone. Part IV. The synthesis of (natural)(+)-α-cyperone, its enantiomorph, and an epimerJournal of the Chemical Society, 1955