109935-57-1

Upstream product

• 103649-64-5 4-nitro-benzoic acid-(1-ethynyl-4t-tert-butyl-cyclohex-r-yl ester) 
• 7103-36-8 trans-4-tert-butyl-1-vinylcyclohexanol 
• 122-04-3 4-nitro-benzoyl chloride 
• 103649-64-5 4-nitro-benzoic acid-(1-ethynyl-4c-tert-butyl-cyclohex-r-yl ester) 

Relevant academic research and scientific papers

Electronic control of enantioselectivity in the palladium-catalyzed asymmetric allylic substitution of trans 4-tbutyl-1-vinylcyclohexyl benzoates

The enantioselectivity in the palladium-catalyzed substitution of allylic benzoates I by sodium dimethylmalonate was influenced by polar and steric effects of the substituents in the phenyl ring of the benzoate. Electron- donating p-substituents afforded