Synthesis of Methyl Dihydrojasmonate. Ester Directed Baeyer-Villiger Oxidation
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918208063687
Reference7 articles.
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3. Oxidation with chlorine complexes. Specific oxidation of secondary hydroxyl groups in the presence of primary hydroxyl groups in polyhydric alcohols.
4. Decarbalkoxylations of geminal diesters, β-keto esters and α-cyano esters effected by sodium chloride in dimethyl sulpoxide
5. Oxygen insertion reactions of bridged bicyclic ketones
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1. A concise synthesis of methyl dihydrojasmonate and methyl (5-methylidene-4-oxocyclopent-2-en-1-yl)acetate from D-glucose;Mendeleev Communications;2024-07
2. The Krapcho Dealkoxycarbonylation Reaction of Esters with α-Electron-Withdrawing Substituents;Organic Reactions;2013-05-30
3. Recent synthetic applications of the dealkoxycarbonylation reaction. Part 2. Dealkoxycarbonylations of β-keto esters, α-cyanoesters and related analogues;Arkivoc;2007-04-12
4. The Baeyer-VilligerOxidation of Ketones and Aldehydes;Organic Reactions;1993-02-04
5. A study of the regioselectivity of oxygen insertion in the Baeyer–Villiger oxidation of bicyclo[2.2.1]heptan-2-ones;J. Chem. Soc., Perkin Trans. 1;1991
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