162708-27-2

Upstream product

• 917-64-6 methyl magnesium iodide 
• 93390-44-4 5-(p-tolyl)-5-oxopentanoic acid methyl ester 
• 833-85-2 5-(4-methylphenyl)-5-oxopentanoic acid 
• 765-43-5 Cyclopropyl methyl ketone 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 33446-33-2 5-Brom-2-(p-tolyl)-2-penten 

Downstream Products

• 162708-28-3 δ,4-dimethylbenzenepentanoic acid 
• 162708-31-8 6-(2-Hydroxy-4-methyl-phenyl)-heptan-2-one 
• 162708-32-9 6-(2-acetoxy-4-methylphenyl)-2-heptanone 

Relevant academic research and scientific papers

Enantioselective Bromolactonization of Trisubstituted Olefinic Acids Catalyzed by Chiral Pyridyl Phosphoramides

Enantioselective bromolactonization of trisubstituted olefinic acids producing synthetically useful chiral lactones with two contiguous asymmetric centers has remained mainly unexplored except for the 6-exo cyclization mode. In this work, the 5-exo- and 6

Synthesis of phenolic sesquiterpenes via oxidative cleavage of benzocycloalkenols

Phenolic sesquiterpenes including sesquichamaenol, 6-(2-hydroxy-4-methylphenyl)-2-methyl-3-heptanone, and curcuphenol methyl ether have been obtained from oxidative cleavage of bicyclic precursors by treatment with acidic hydrogen peroxide in a process wh