745813-71-2

Upstream product

• 98-86-2 acetophenone 
• 745813-62-1 (-)-(2S,3S)-3-methyl-2-phenyl-4-penten-2-ol 
• 884497-15-8 (2R,3S)-methyl 3-hydroxy-2-methyl-3-phenylbutanoate 
• 14366-96-2 threo-3-Phenyl-2-methyl-butan-1,3-diol 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant academic research and scientific papers

Highly diastereo- and enantioselective copper-catalyzed domino reduction/aldol reaction of ketones with methyl acrylate

(Chemical Equation Presented) A good choice: A new catalytic method was found for the construction of stereogenic quaternary carbon centers through a copper-catalyzed domino conjugated reduction/aldol reaction of methyl acrylate with various alkyl aryl ke

Catalytic enantioselective allylboration of ketones

The first example of catalytic enantioselective allylboration and crotylboration of simple ketones is described. High enantioselectivity (up to 93% ee) was obtained using 3 mol % CuF-iPr-DuPHOS as a chiral catalyst and 4.5 mol % La(Oi/sup