32137-28-3Relevant academic research and scientific papers
Concise Formal Synthesis of the Pseudopterosins via Anionic Oxy-Cope/Transannular Michael Addition Cascade
Ramella, Vincenzo,Roosen, Philipp C.,Vanderwal, Christopher D.
, p. 2883 - 2886 (2020)
An anionic oxy-Cope/transannular Michael addition cascade converts a spirocyclic architecture - readily available by Diels-Alder cycloaddition - into the hydrophenalene carbon skeleton of the pseudopterosin aglycones. Oxidation of the resulting cyclohexen
NOVEL FLAVORING AGENTS COMPRISING 2-ALKYLIDENE-METHYLCYCLOHEXANONE BASED COMPOUNDS
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Paragraph 0024; 0025, (2019/12/31)
PROBLEM TO BE SOLVED: To provide flavoring agents or flavoring agent compositions that impart a taste such as sweetness and a flavor with spicy and herb feelings, and have a more natural feeling. SOLUTION: The flavoring agent compounds are compounds repre
Thermolysis of alkylated 2-cyclohexenones and related monoterpenoid ketones
Lange, Gordon L.,Pereira, Vincent A.,Weedle, Michael
, p. 1639 - 1644 (2007/10/02)
2-Cyclohexenone and three methylated cyclohexenones were thermolyzed at 400 deg C for 20 hours to give conversions to products in the range 11 to 45 percent.When three monoterpenes containing the cyclohexenone moiety were thermolyzed under the same conditions the conversions were over 75 percent.The major products formed were alkylated benzenes, alkylated phenols, and double bond isomers of the starting enones.Mechanisms are proposed to account for these products.
