Synthesis of Methyl Dihydrojasmonate. Ester Directed Baeyer-Villiger Oxidation
- 1 January 1982
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 12 (7) , 501-505
- https://doi.org/10.1080/00397918208063687
Abstract
The distinguished organoleptic properties of the jasmonoids have helped foment development of synthetic routes.1 In one of our recent approaches to methyl dihydrojasmonate (1) we assimulated and integrated the acid-catalyzed rearrangement process2 of cyclopentadiene-acrylic acid adducts into our scheme.Keywords
This publication has 7 references indexed in Scilit:
- Oxygen insertion reactions of bridged bicyclic ketonesTetrahedron, 1981
- Total synthesis of racemic 12-methylprostaglandinsJournal of the American Chemical Society, 1977
- Oxidation with chlorine complexes. Specific oxidation of secondary hydroxyl groups in the presence of primary hydroxyl groups in polyhydric alcohols.Tetrahedron Letters, 1974
- Synthesis of Jasmonoids, a ReviewSynthetic Communications, 1974
- Decarbalkoxylations of geminal diesters, β-keto esters and α-cyano esters effected by sodium chloride in dimethyl sulpoxideTetrahedron Letters, 1973
- Synthesis of endo-2-Carboxy-endo-6-aminonorbornane Lactam1The Journal of Organic Chemistry, 1961
- Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, IX: Zur Kenntnis der bei der Hydratisierung von Bicyclo‐[1.2.2]‐hepten‐carbonsäuren entstehenden LactoneEuropean Journal of Inorganic Chemistry, 1961