Synthese totale et stereoselective du dimethyl-6,10 methylidene-9 undecene-5 (e) one-2: un des constituants de l'huile de Costus
- 1 January 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (50) , 5275-5278
- https://doi.org/10.1016/s0040-4039(00)85817-7
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Isolation and total synthesis of (E)‐6, 10‐dimethyl‐9‐methylidene‐undec‐5‐en‐2‐one, a constituent of Costus root oilHelvetica Chimica Acta, 1978
- A novel terminal functionalization of farnesol and related polyisoprenoids. Application to the synthesis of solanesolTetrahedron Letters, 1978
- (E)-9-isopropyl-6-methyldeca-5,9-dien-2-one, a terpenoid C14-ketone with a novel skeletonJournal of the Chemical Society, Chemical Communications, 1977
- ALLYLIC CHLORIDES FROM ALLYLIC ALCOHOLS: GERANYL CHLORIDEOrganic Syntheses, 1974
- A new synthesis of α,β-unsaturated aldehydes including (e)2-methyl-2-alkenalTetrahedron Letters, 1973
- Improved procedure for oxidations with the chromium trioxide-pyridine complexThe Journal of Organic Chemistry, 1970
- A New Method for the Alkylation of Ketones and Aldehydes: the C-Alkylation of the Magnesium Salts of N-Substituted IminesJournal of the American Chemical Society, 1963
- The Wittig Reaction Using Methylsulfinyl Carbanion-Dimethyl Sulfoxide 1The Journal of Organic Chemistry, 1963