71492-92-7

Upstream product

• 676-58-4 methylmagnesium chloride 
• 71313-48-9 3-(cyclohex-1-en-1-yl)prop-2-yn-1-yl 4-methylbenzenesulfonate 

Downstream Products

• 72393-60-3 3-(Cyclohexen-1-yl)-trimethylsilylbutadien-1,2 
• 72393-49-8 2-(Cyclohexen-1-yl)-heptadien-2,3 
• 71493-00-0 3-(2-Propylcyclohexyliden)-butin-1 
• 72393-61-4 3(Cyclohexen-1-yl)-1-thiophenoxy-butadien-1,2 
• 71492-53-0 2-(Cyclohexen-1-yl)-ethinyl-2-penten-4 
• 72393-62-5 2(Cyclohexen-1-yl)-2-ethinyl-1-phenyl-propanol-1 
• 72393-50-1 4(Cyclohexen-1-yl)-1-phenyl-pentadien-2,3-ol-1 
• 71492-57-4 2-(Cyclohexen-1-yl)-dodecadien-2,3-in-6 
• 72393-66-9 2(Cyclohexen-1-yl)dodecin-3-ol-5 
• 72393-57-8 2-(Cyclohexen-1-yl)-hexadien-2,3-on-5 

Relevant academic research and scientific papers

OBTENTION DE CYCLOPENTENONES PAR ACETOXYMERCURATION ET ECETOXYTHALLATION DE VINYLALLENES

Eight variously substituted vinylallenes were converted to cyclopentenones by acetoxymercuration (yields 50-80percent) and acetoxythallation (yields 25-68percent).These two reactions are rapid and purification of the products was easy.The demetallation step is particularly favourable and is spontaneous in acetic acid.The reaction of magnesiocuprates with the sulfonates of 4-ene 2-yne-1 ols is a rapid and simple method for tbe synthesis of vinylallenic hydrocarbons.