79815-46-6

Upstream product

• 79803-40-0 dimethyl cis-2,6-diphenyl-4,4-ethylenedioxycyclohexane-1,1-dicarboxylate 
• 54105-33-8 dimethyl cis-2,6-diphenyl-4-oxocyclohexane-1,1-dicarboxylate 
• 79803-41-1 methyl trans-2,6-diphenyl-4,4-ethylenedioxycyclohexane-1-carboxylate 
• 79803-42-2 trans-2,6-diphenyl-4,4-ethylenedioxycyclohexane-1-carboxylic acid 
• 79803-35-3 methyl trans-2,6-diphenyl-4-oxocyclohexane-1-carboxylate 
• 538-58-9 1,5-diphenyl-1,4-pentadiene-3-one 
• 41167-36-6 dimethyl 4-oxo-2,6-diphenylcyclohexane-1,1-dicarboxylate 
• 871884-02-5 4-oxo-2,6-diphenyl-cyclohexane-1,1-dicarboxylic acid 

Downstream Products

• 79803-35-3 4-oxo-2,6-diphenyl-cyclohexanecarboxylic acid methyl ester 

Relevant academic research and scientific papers

Cyclohexanone gem-dicarboxylates - Versatile intermediates for fused heterocycles

The reactivity of gem-ester group in cyclohexanone-1,1-dicarboxylates (1) was studied by reaction with Cu/quinoline and ceric ammonium nitrate. The resultant cyclohexanone-1-carboxylic acids (2) and cyclohexan-1,4-diones (3) were made use to develop selen

Saponification of Dimethyl cis-2,6-Diphenyl-4-oxocyclohexane-1,1-dicarboxylate. A Reinvestigation

The saponification of dimethyl cis-2,6-diphenyl-4-oxocyclohexane-1,1-dicarboxylate was reported over 50 years ago to produce the corresponding diacid.The ease with which the reaction occurred is surprising considering the steric factors involved.We have f