65979-78-4

Upstream product

• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 1666-13-3 diphenyl diselenide 
• 71098-88-9 N-phenylselanylphthalimide 
• 583-60-8 2-Methylcyclohexanone 
• 19980-35-9 1-trimethylsilyloxy-2-methyl-1-cyclohexene 
• 34837-55-3 Phenylselenyl bromide 
• 5707-04-0 Phenylselenyl chloride 

Downstream Products

• 42858-46-8 2-phenylseleno-6-methylcyclohexanone 
• 54322-98-4 (2RS,1'RS)-2-((Hydroxyphenyl)methyl)-2-methylcyclohexanone 
• 54322-98-4 (2RS,1'SR)-2-((Hydroxyphenyl)methyl)-2-methylcyclohexanone 
• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 3045-98-5 2-methylenecyclohexanone 
• 6610-21-5 6-methylcyclohex-2-en-1-one 
• 7443-52-9 (+/-)-trans-2-methylcyclohexanol 
• 220758-02-1 1,1-(ethylenedioxy)-3-(10-hydroxydecyl)-2-methyl-3-(phenylsulfonyl)-cyclohexane 
• 220758-00-9 1,1-(ethylenedioxy)-2-methyl-3-(phenylsulfonyl)-cyclohexane 
• 220757-98-2 2-methyl-3-(phenylsulfonyl)-cyclohexan-1-one 

Relevant academic research and scientific papers

Effect of cyclohexenonic long chain fatty alcohols on neurite outgrowth. Study on structure-activity relationship

Four series of long chain fatty alcohols bearing a cyclohexenone moiety in addition to a ω-alkanol side chain were synthesized using 'Umpolung' reactivity strategy. Their effect on neurite outgrowth was evaluated by means of fetal rat neurons in culture. The length of the ω-hydroxy side chain is a crucial factor for biological activity.

N-(Phenylseleno)Phthalimide: A Useful Reagent For The α-Selenylation Of Ketones And Aldehydes.

Α-phenylselenoketones and α-phenylselenoaldehydes are obtained with a good regioselectivity by treatment of the corresponding ketones or aldehydes with N-(phenylseleno)phthalimide and p-toluenesulfonic acid. - Key words: Ketones, α-phenylselenoketones, N-

A DIRECT ARYLSELENENYLATION OF ENONES WITH DIARYL DISELENIDES BY A ELECTROREDUCTIVE PROCEDURE

A new procedure for arylselenenylation of enones has been developed by electrolysis with diaryl diselenide and chlorotrimethylsilane in methanol.In the course of the reaction generation of aryl selenols in situ is assumed.