884495-99-2

Upstream product

• 7333-63-3 4-bromobutylphosphonium bromide 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 1114779-86-0 (4-chlorophenyl)[1-(phenylselanyl)cyclobutyl]methanone 
• 1127971-75-8 C₁₁H₁₁ClO 
• 104-88-1 4-chlorobenzaldehyde 
• 95-14-7 1,2,3-Benzotriazole 
• 1127971-32-7 C₁₇H₁₄ClN₃O₂ 
• 1127972-03-5 C₁₇H₁₆ClN₃O₂ 
• 1321621-48-0 C₁₁H₁₁ClO₂ 
• 1322744-63-7 C₁₁H₁₂BrClO 
• 1028938-79-5 1-(2-(4-chlorophenyl)cyclopent-2-enyl)ethanone 
• 1028938-80-8 1-(2-(4-chlorophenyl)cyclopent-2-enyl)propan-1-one 
• 884496-07-5 (+)-(R)-2-(4-chlorophenyl)-1-oxaspiro[2.3]hexane 

Relevant academic research and scientific papers

Enantioselective synthesis of 2-aryl cyclopentanones by asymmetric epoxidation and epoxide rearrangement

(Chemical Equation Presented) Optically active epoxides are prepared by the highly enantioselective epoxidation of benzylidenecyclobutanes using a glucose-derived ketone as the catalyst and oxone as the oxidant. A subsequent Lewis acid catalyzed rearrange