59697-64-2

Upstream product

• 78344-00-0 (6-oxocyclohex-1-en-1-yl)-2-ethyl acetate 
• 1119-51-3 bromopentene 
• 930-68-7 cyclohexenone 
• 74457-11-7 2-(1-Hydroxy-ethyl)-3-phenylsulfanyl-cyclohexanone 
• 74457-12-8 2-(1-hydroxyethyl)-3-(methylseleno)cyclohexanone 
• 67720-34-7 2-(1-hydroxyethyl)-2-cyclohexen-1-one 
• 55998-95-3 erythro-2-(1'-Hydroxyethyl)-3-methylcyclohexan-1-on 
• 59697-60-8 nona-2t,8-dien-4-one 

Downstream Products

• 75731-87-2 (4-Bromo-phenyl)-carbamic acid (R)-3-methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enylmethyl ester 
• 75731-91-8 (TT)-1,3-dimethyl-2-ethylcyclohexanol 
• 75766-24-4 (CC)-1,3-dimethyl-2-ethylcyclohexanol 
• 75731-82-7 (1R,3R)-2-Eth-(E)-ylidene-1,3-dimethyl-cyclohexanol 
• 75731-86-1 [(R)-3-Methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enyl]-methanol 
• 75731-88-3 [(S)-3-Methyl-2-((R)-1-methyl-pentyl)-cyclohex-1-enyl]-methanol 

Relevant academic research and scientific papers

Aldol Reaction of Aluminium Enolate Resulting from 1,4-Addition of R2AlX to α,β-Unsaturated Carbonyl Compound. A 1-Acylethenyl Anion Equivalent

Organoaluminium reagents R2AlX (X=SPh, SeMe) easily add to α,β-unsaturated carbonyl compounds in 1,4-fashion.The resulting aluminium enolates react with aldehydes to give aldol adducts in fair to good yields.Formal elimination of HX from the adducts provi