84451-81-0

Downstream Products

• 139040-30-5 6-Hydroxy-r-1,c-5-dimethyl-c-6-phenylbicyclo<3.3.0>octan-2-on 
• 139040-25-8 r-1,c-5-Dimethyl-t-2,c-6-diphenylbicyclo<3.3.0>octan-2,6-diol 
• 139069-70-8 r-1,c-5-Dimethyl-t-2,6-diphenylbicyclo<3.3.0>oct-6-en-2-ol 
• 139040-33-8 r-1,c-5-Dimethyl-c-2,6-diphenylbicyclo<3.3.0>oct-6-en-2-ol 
• 139040-34-9 2,6-Dimethyl-5-phenyl-1-trimethylsilyloxy-9-oxatricyclo<3.3.1.0^2,6>nonan 
• 139040-32-7 2,6-Dimethyl-1,5-diphenyl-9-oxatricyclo<3.3.1.0^2,6>nonan 
• 717839-42-4 r-1,c-5-Dimethyl-2,6-diphenylbicyclo<3.3.0>octa-2,6-dien 
• 139040-31-6 r-1,c-5-Dimethyl-6-phenylbicyclo<3.3.0>oct-6-en-2-on 

Relevant academic research and scientific papers

Dependence of the Lewis Acid-induced Reaction of β-stannyl Ketones upon Substitution Pattern. 1,2-Alkyl Migration versus Cyclopropanation

3-Stannylcyclohexanones fully substituted at 2 and 3 positions undergo a 1,2-alkyl migration and cyclopropanation.The balance of the reaction pattern depends upon the steric environment and migratory aptitude of the alkyl groups.