42466-74-0

Upstream product

• 917-64-6 methyl magnesium iodide 
• 7474-65-9 (E)-2-phenylchalcone 
• 20432-26-2 2-phenyl-trans-crotonic acid 
• 71-43-2 benzene 
• 4023-77-2 1-benzoyl-1,2-diphenylethylene 
• 451-40-1 phenyl benzyl ketone 
• 585-71-7 (1-bromoethyl)benzne 
• 6333-99-9 erythro-3-benzoyl-2,3-diphenylpropane 
• 51760-87-3 (+/-)-erythro-2,3-diphenyl-butyryl chloride 
• 28557-00-8 phenylzinc chloride 
• 7647-01-0 hydrogenchloride 
• 6333-99-9 (+/-)-erythro-1,2,3-triphenyl-butan-1-one 
• 64-19-7 acetic acid 
• 141-52-6 sodium ethanolate 

Downstream Products

• 6333-99-9 (+/-)-threo-1,2,3-triphenyl-butan-1-one 
• 6333-99-9 threo-3-benzoyl-2,3-diphenylpropane 

Relevant academic research and scientific papers

Epimerization and Kinetic Protonation as Factors Determining the Stereochemistry of the Michael Reaction

Model compounds in which the only possibility for isomerization is epimerization were synthesized.They undergo isomerization under the conditions widely used in the Michael addition.Conclusions are drawn as to the possibilities for epimerization or kineti