133017-22-8

Upstream product

• 108-93-0 cyclohexanol 
• 621-13-6 dicyclohexyl trans-butenedioate 
• 140850-35-7 (-)-dicyclohexyl tartrate 
• 15785-59-8 dicyclohexyl tartrate 

Downstream Products

• 668461-63-0 (2E)-N-benzhydryl-5-amino-5-cyclohexyloxycarbonyl-2-(4-methoxyphenyl)pent-2-enal 
• 668461-64-1 N-benzhydryl-5-(4-methoxyphenyl)-1,2,3,4-tetrahydro-pyridine-2-carboxylic acid cyclohexyl ester 
• 838828-57-2 (2E)-N-(2,4-dimethyl-6-iodophenyl)-5-amino-5-cyclohexylcarbonyl-2-methyl-2-penten-1-ol acetate 
• 838828-49-2 (2E)-N-(2,4-dimethyl-6-iodophenyl)-5-amino-5-cyclohexylcarbonyl-2-methylpent-2-en-1-nal 
• 198693-91-3 2-Hydroxy-4-(4-methoxy-benzyloxymethyl)-5-methyl-hex-4-enoic acid cyclohexyl ester 

Relevant academic research and scientific papers

Palladium-catalyzed intramolecular coupling between aryl iodides and allyl moieties via thermal and microwave-assisted conditions

Palladium-catalyzed intramolecular cross-coupling reactions between aryl iodides and allyl moieties were successfully demonstrated in the presence of palladium catalyst, tri-o-tolylphosphine, a tertiary amine, and water. Several kinds of trans-2,4-disubst

A Useful Synthesis of Chiral Glyoxylates

A convenient synthesis of the cyclohexyl, (1R,3R,4S)-3-p-methyl and (1S-endo)-2-bornyl glyoxylates, from the respective alcohols and other very available materials, as a model applicable to that of other chiral, sensitive glyoxylates, is described.