91899-75-1

Upstream product

• 93022-03-8 2-hydroxy-1,3-diphenyl-but-3-en-1-one 
• 124-41-4 sodium methylate 
• 66364-97-4 1,3-Diphenyl-3-chloro-2-hydroxy-1-butanone 
• 19804-64-9 cis-(3-methyl-3-phenyloxiran-2-yl)(phenyl)methanone 
• 19804-64-9 trans-(3-methyl-3-phenyloxiran-2-yl)(phenyl)methanone 
• 7647-01-0 hydrogenchloride 
• 1533-20-6 1,3-diphenylbutane-1-one 
• 19513-91-8 (E)-4-bromo-2,3-epoxy-1,3-diphenyl-1-butanone 
• 70729-30-5 1,3-Diphenyl-3-chloro-2-hydroxy-1-butanone 
• 101118-69-8 (2RS,3SR)-3,4-dibromo-2-hydroxy-1,3-diphenyl-butan-1-one 
• 54435-79-9 (E)-1,3-diphenyl-3-methyl-2-propen-1-one 
• 1074-12-0 phenylglyoxal hydrate 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Relevant academic research and scientific papers

The Effect of Lewis Acid and Solvent on Concerted 1,2-Acyl Migration

Lewis acid catalyzed 1,2-benzoyl migration in (E)- and (Z)-1,3-diphenyl-2-buten-1-on oxides (dypnone oxides) is a concerted process that occurs with inversion of configuration at the migration terminus when nonpolar solvents are employed.In methanol solve

Thermal Rearrangement of trans-2,3-Epoxy-1,3-diphenylbutan-1-one. A Concerted 1,2-Carbonyl Migration

The thermal rearrangement of a chiral α,β-epoxyketone is a concerted process that proceeds without loss of optical activity and with inversion of configuration at the migration terminus.