147295-33-8

Upstream product

• 122-00-9 para-methylacetophenone 
• 138371-74-1 4-methyl-4-(p-tolyl)cyclohex-2-en-1-one 
• 33596-66-6 2-(4-methylphenyl)propanal 
• 36553-42-1 ethyl β-methyl-β-(p-methylphenyl)glycidate 
• 75-77-4 chloro-trimethyl-silane 
• 138371-75-2 4-methyl-4-para-tolylcyclohexanone 

Downstream Products

• 93862-61-4 (R)-2-Methyl-5-oxo-2-p-tolyl-cyclopentanecarboxylic acid methyl ester 
• 86505-48-8 (R)-3-methyl-3-(p-tolyl)cyclopentan-1-one 
• 116384-94-2 (R)-3-Methyl-3-p-tolyl-hexanedioic acid dimethyl ester 
• 147295-36-1 (R)-4-Methyl-2-oxo-4-p-tolyl-cyclopentanecarboxylic acid methyl ester 

Relevant academic research and scientific papers

Construction of a Chiral Quaternary Carbon Center by Enantioselective Deprotonation: Application to the Formal Synthesis of (+)-α-Cuparenone

Construction of a chiral quaternary carbon center was achieved by employing an enantioselective deprotonation with chiral bases and this strategy was applied to the formal synthesis of (+)-α-cuparenone.