129315-83-9

Upstream product

• 129315-76-0 2-(4-chlorophenyl)-2-phenylcyclopentanone 
• 21771-88-0 α-(4-chlorophenyl)phenylacetic acid 
• 28523-15-1 2-(4-chlorophenyl)-2-phenylacetaldehyde 
• 139952-10-6 3-(4-chlorophenyl)-3-phenylcyclopentene 
• 134-85-0 4-chlorobenzophenone 
• 129315-96-4 2-(4-chlorophenyl)-2-phenyl-4-pentenoic acid 
• 129315-93-1 2-(4-chlorophenyl)-2-phenylcyclopent-4-enone 
• 53780-26-0 2-(4-chlorophenyl)-2-phenyloxirane 
• 139952-14-0 (1R,2R,5S)-2-(4-Chloro-phenyl)-2-phenyl-6-oxa-bicyclo[3.1.0]hexane 

Relevant academic research and scientific papers

Evidence for stereoelectronic control in the epoxidation of sterically unbiased 3,3-diarylcyclopentenes

Epoxidations of the sterically unbiased olefin, 3-(4-X-phenyl)-3-phenylcyclopentene (X = NO2, Br, Cl, OCH3) with peracetic acid have been found to proceed with up to 73.27 stereoselectivity. Stereochemistry of the products was determ

Diastereoselectivity in the reduction of sterically unbiased 2,2-diarylcyclopentanones

Reduction of sterically unbiased 2-phenyl-2-(4-X-phenyl)cyclopentanones 1 (X = NO2, Br, Cl, OCH3, OH, NH2) with either sodium borohydride in methanol or lithium borohydride in tetrahydrofuran at 0°C produced diastereomeric