345929-69-3

Upstream product

• 7103-36-8 trans-4-tert-butyl-1-vinylcyclohexanol 
• 85390-65-4 cis-4-tert-butyl-1-vinylcyclohexyl acetate 
• 108-59-8 malonic acid dimethyl ester 
• 85390-64-3 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol acetate 
• 996-82-7 sodium diethylmalonate 
• 128550-79-8 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol 2-methoxybenzoate 
• 128550-80-1 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol 4-methoxybenzoate 
• 128550-82-3 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol 4-bromobenzoate 
• 128550-74-3 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol benzoate 
• 18424-76-5 dimethyl malonate sodium salt 
• 128550-84-5 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol 2-naphthoate 
• 128550-83-4 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol 1-naphthoate 
• 128550-77-6 trans-1-Ethenyl-4-(1,1-dimethylethyl)cyclohexanol dimethylcarbamate 

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

Substrate Leaving Group Control of the Enantioselectivity in the Palladium-Catalyzed Asymmetric Allylic Substitution of 4-Alkyl-1-vinylcyclohexyl Derivatives

The strong influence of the nature of the leaving group in allylic derivatives in their enantioselective Pd-catalyzed substitution by nucleophile is reported.Analysis of the stereochemical course of the Pd-catalyzed substitution of achiral trans-4-tert-bu