66221-12-3

Upstream product

• 70412-29-2 3-(2-methyl-1,3-diphenyl-2-cyclopropen-1-yl)-1-butene 
• 66221-11-2 endo-3,6-dimethyl-1,2-diphenyltricyclo<2.2.0.0^2,6>hexane 
• 73377-63-6 tert-butyl 1-methyl-2,3-diphenyl-2-cyclopropene-1-acetate 
• 72612-89-6 3-methyl-1,2-diphenylcyclopropenylium perchlorate 

Downstream Products

• 70840-44-7 (Z)-1-(2-methyl-1,3-diphenyl-2-cyclopropen-1-yl)-2-butene 
• 66221-09-8 (E)-1-(2-methyl-1,3-diphenyl-2-cyclopropen-1-yl)-2-butene 
• 70412-29-2 3-(2-methyl-1,3-diphenyl-2-cyclopropen-1-yl)-1-butene 
• 73464-49-0 endo-3,6-dimethyl-1,2-diphenylbicyclo<3,1,0>hex-2-ene 
• 66221-11-2 endo-3,6-dimethyl-1,2-diphenyltricyclo<2.2.0.0^2,6>hexane 
• 73377-61-4 exo-3,6-dimethyl-1,2-diphenylbicyclo<3.1.0>hex-2-ene 
• 66221-11-2 exo-3,6-dimethyl-1,2-diphenyltricyclo<2.2.0.0^2,6>hexane 

Relevant academic research and scientific papers

Thermal Isomerization of Allyl-Substituted Cyclopropenes. An Example of a Nonsynchronous Cope Rearrangement

The thermal Cope rearrangement of a number of allyl-substituted cyclopropenes has been studied in mechanistic detail.Thermolysis of 1,2-diphenyl-3-allyl-3-methylcyclopropene produced an equilibrium mixture of recovered starting material (35percent), 1,3-d