60433-18-3

Upstream product

• 6668-24-2 2-methyl-1-phenyl-1,3-butanedione 
• 100-39-0 benzyl bromide 
• 28918-08-3 2-benzyl-1-phenylbutane-1,3-dione 
• 74-88-4 methyl iodide 
• 93-91-4 1-phenylbutan-1,3-dione 

Downstream Products

• 74971-19-0 4-benzyl-3,4-dimethyl-5-phenylisopyrazole 
• 74971-31-6 endo-9-benzyl-7,8-diaza-1,9-dimethyl-6-phenyltricyclo<4.2.1.0^2,5>non-7-ene 
• 74971-26-9 endo-9-benzyl-7,8-diaza-1,9-dimethyl-6-phenyltricyclo<4.2.1.0^2,5>nona-3,7-diene 
• 74971-34-9 anti-3-benzyl-2,3-dimethyl-4-phenyltricyclo<3.2.0.0^2,4>heptane 

Relevant academic research and scientific papers

Reactions of copper(II) β-diketonates under free radical conditions. Preparation of highly congested β-diketones

Copper(II) β-diketonates react with alkyl bromides under free radical conditions to give highly congested β-diketones such as 3-(1-adamantyl)-3-alkylpentane-2,4-diones. Another typical free radical reagent: benzoyl peroxide, reacts also functionalizing the intercarbonyl positions.

Regio- and Stereoselective 1,2 Wagner-Meerwein Shifts during Trifluoroacetic Acid Catalyzed Isomerization of Unsymmetrically Substituted Tricyclo2,4>heptanes

The regioselectivity and stereoselectivity which materialize upon trifluoroacetic acid promoted isomerization of variously substituted tricyclo2,4>heptanes have been experimentally determined.The highly strained hydrocarbon substrates h