20780-33-0

Upstream product

• 74456-85-2 N-((2R,6R)-2,6-Diphenyl-cyclohexylidene)-N'-phenyl-hydrazine 
• 83324-28-1 Phenyl-(6-phenyl-cyclohex-1-enyl)-diazene 
• 1201786-60-8 6-bromo-1,2,3,4-tetrahydro-1,1'-biphenyl 
• 1542147-98-7 (S)-1-(1,4,5,6-tetrahydro-[1,1'-biphenyl]-2-yl)ethanone 
• 1542147-92-1 (S)-6-bromo-1,2,3,4-tetrahydro-1,1'-biphenyl 
• 1542147-96-5 C₁₄H₁₈O 
• 1444-65-1 (RS)-2-phenylcyclohexanone 

Downstream Products

• 20834-02-0 cis-2,6-diphenylcyclohexanone 

Relevant academic research and scientific papers

Synthesis of trans -2,6-disubstituted cyclohexanones through allylic substitution

trans-2,6-Disubstituted cyclohexanones were synthesized with high regio- and stereoselectivity by allylic substitution followed by ozonolysis. Both alkyl and aryl groups were successfully installed to the cyclohexane ring. The stereochemistry of the Ssub

Reactions of Cojugated Arylazocycloalkenes with Grignard Reagents. Part 3. A Convenient Synthesis of 2,6-Diaryl- and 2-Alkyl-6-aryl-cyclohexanones

A synthesis of the title compounds with the substituents at C-2 and C-6 trans to each other is described. 2-Arylcyclohexanones were converted into 1-phenylazo-6-arylcyclohexenes, which by reaction with Grignard reagents led to trans-2,6-diaryl- and trans-