A method for the stereoselective introduction of angular methyl groups
- 31 December 1968
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 9 (15) , 1899-1901
- https://doi.org/10.1016/s0040-4039(00)76388-x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Stereospecific introduction of a vicinally functionalized angular methyl group. A synthesis of 1-valeranoneJournal of the American Chemical Society, 1967
- Experiments Directed toward the Total Synthesis of Terpenes. VIII. The Total Synthesis of (±)-Kaurene and (±)-Atisirene1The Journal of Organic Chemistry, 1966
- Experiments Directed toward the Total Synthesis of Terpenes. VII. The Synthesis of (±)-8β-Carbomethoxy-13-oxopodocarpanone, a Degradation Product of Phyllocladene1The Journal of Organic Chemistry, 1966
- Conjugate Addition of Methylmagnesium Iodide to 10-Methyl-1(9)-octal-2-one. An Approach to the Valeranone Carbon FrameworkThe Journal of Organic Chemistry, 1966
- The preparation and properties of tris(triphenylphosphine)halogenorhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivativesJ. Chem. Soc. A, 1966
- The Chemistry of Carbanions. X. The Selective Alkylation of Unsymmetrical Ketones1The Journal of Organic Chemistry, 1965
- Organic syntheses by means of noble metal compounds XXI. Decarbonylation of aldehydes using rhodium complexTetrahedron Letters, 1965
- Total synthesis of methyl (±)-8α-carboxymethylpodocarpan-13-one-4β-carboxylate, a degradation product of steviolTetrahedron Letters, 1965
- Photochemical Reactions. XIII.1 A Total Synthesis of (±)-ThujopseneJournal of the American Chemical Society, 1964
- Stereospecific Angular Alkylation. A New Application of the Claisen Rearrangement1Journal of the American Chemical Society, 1961