28354-98-5

Upstream product

• 24543-41-7 β-Pyronen 
• 76514-91-5 2,3,4,4-tetramethylcyclohex-1-en-1-yl trimethylsilyl ether 
• 204578-10-9 1,2-epoxy-1,5,5-trimethyl-6-methylenecyclohexane 
• 50405-45-3 4-hydroxy-5,6-dimethyl-2H-pyran-2-one 
• 514-95-4 1,5,5-trimethyl-6-methylene-cyclohexene 
• 204578-11-0 3-bromomethyl-2,4,4-trimethyl-2-cyclohexenol 
• 13395-71-6 2,4,4-trimethyl-2-cyclohexenone 

Downstream Products

• 3019-82-7 2,3,4,4-tetramethyl-2-cyclohexen-1-ol 
• 514-95-4 1,5,5-trimethyl-6-methylene-cyclohexene 
• 514-96-5 β-pyronene 
• 28353-86-8 2,3,4,4-tetramethylcyclohexanone 
• 28353-84-6 2,3,4,4-Tetramethyl-cyclohexanol-1 

Relevant academic research and scientific papers

Synthetic studies on breviones: Construction of the CDE ring system

Breviones A-E (1-5), allelopathic agents isolated from Penicillium brevicompactum Dierckx, are structurally unique pentacyclic or hexacyclic diterpenoid derivatives. The synthesis of a structurally simplified model compound (8), corresponding to the chara

γ-Pyronene, a synthon derived from saffron and intermediary precursor of synthesis of forskolin and strigol

γ-Pyronene, a terpenic synthon available from myrcene, is an excellent raw material for the preparation of numerous intermediates used in the synthesis of perfumes, retinoids and biological derivatives such as forskolin or strigol.

Alkyl Substituent Effects on the Photorearrangement of Cyclohex-2-en-1-ones to Lumiketones

The effect of alkyl substitution on the photorearrangement of cyclohex-2-en-1-ones to bicyclohexan-2-ones (lumiketones) was investigated.Contrary to earlier reports, both 2,4,4- and 3,4,4-trimethylcyclohex-2-en-1-one undergo this rearrangement upon