52121-66-1

Upstream product

• 765-42-4 1-cyclopropylethanol 
• 105-13-5 4-Methoxybenzyl alcohol 
• 123-11-5 4-methoxy-benzaldehyde 
• 765-43-5 Cyclopropyl methyl ketone 
• 824-94-2 p-methoxybenzyl chloride 
• 72881-75-5 2-(4-Methoxyphenyl)-vinyl-cyclopropyl-keton 
• 87141-66-0 1-Cyclopropyl-3-(4-methoxy-phenyl)-propan-1-one 
• 72881-75-5 (E)-1-cyclopropyl-3-(4-methoxyphenyl)prop-2-en-1-one 

Downstream Products

• 75682-89-2 1-[(E)-6-(4-Methoxy-phenyl)-hex-3-enyl]-6-methyl-7-oxa-bicyclo[4.1.0]heptan-2-one 
• 75682-92-7 2-[(E)-6-(4-Methoxy-phenyl)-hex-3-enyl]-1,3-dimethyl-cyclohex-2-enol 
• 52121-86-5 6-(4-methoxyphenyl)-3-hexenyl bromide 
• 75682-86-9 2-[(E)-6-(4-Methoxy-phenyl)-hex-3-enyl]-3-methyl-cyclohex-2-enone 

Relevant academic research and scientific papers

Nickel-catalyzed guerbet type reaction: C-alkylation of secondary alcohols via double (de)hydrogenation

Acceptorless double dehydrogenative cross-coupling of secondary and primary alcohols under nickel catalysis is reported. This Guerbet type reaction provides an atom- and a step-economical method for the C-alkylation of secondary alcohols under mild, benign conditions. A broad range of substrates including aromatic, cyclic, acyclic, and aliphatic alcohols was well tolerated. Interestingly, the C-alkylation of cholesterol derivatives and the double C-alkylation of cyclopentanol with various alcohols were also demonstrated.

3-Methylcyclohex-2-enone Derivatives as Initiators of Cyclisation. Part 4. Some Bicyclisations

Hydrochrysene and hydrophenanthrene derivatives (8)-(14) have been prepared by cyclisation of 2-substituted 3-methylcyclohexen-2-ones and the derived 2,3-epoxides.Cyclisation of the epoxides does not give preparatively useful yields of bicyclised compound

Aryl substituted diketones

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Dialkylaminophenylethyl (or vinyl) cyclopropyl carbinols

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester. The intermediate iodides are prepared by cond

Methylenedioxyphenyl substituted aliphatic diketones

Aryl substituted diketones and keto-esters, useful as antiviral agents and insecticides, are prepared by reacting an arylalkyl or arylalkenyl iodide with a metal salt of the appropriate diketone or keto-ester.

Aryl substituted ketones

Aryl substituted tertiary carbinols, useful as antiviral agents and insecticides, are prepared by reacting the Grignard reagent derived from an arylalkyl or arylalkenyl iodide with a dialkyl ketone or an alkyl alkenyl ketone; or by reacting an arylalkyl or arylalkenyl ketone with an alkyl- or alkenylmagnesium halide.

Antivital activity of some β diketones. I. Aryl alkyl diketones. In vitro activity against both RNA and DNA viruses

The discovery that 4 [3 ethyl 6 [(3,4 methylenedioxy)phenyl] 3 hexenyl] 3,5 heptanedione exhibited an in vitro inhibitory effect against equine rhinovirus led to a structure activity study to establish the criteria for optimum activity. Modification of th