182360-62-9

Upstream product

• 182511-39-3 (S)-2-(3-oxo-1,3-diphenyl-propyl)-malonic acid diethyl ester 
• 942129-14-8 (E)-2-(3-phenylprop-2-enoyl)pyridine-1-oxide 
• 1338699-01-6 C₁₉H₁₉NO₆ 
• 108-59-8 malonic acid dimethyl ester 
• 164931-80-0 (S)-(3-oxo-1,3-diphenyl-propyl)-malonic acid dimethyl ester 
• 5292-53-5 diethyl benzalmalonate 
• 6626-84-2 dimethyl 2-benzylidenepropanedioate 

Downstream Products

• 182360-64-1 2-((S)-2-Chlorocarbonyl-1-phenyl-ethyl)-malonic acid dimethyl ester 
• 359876-02-1 dimethyl (S)-(-)-4-oxo-2-phenyl-1,1-pentanedicarboxylate 
• 108056-64-0 (S)-5-oxo-3-phenylhexanoic acid 
• 108056-65-1 methyl (S)-(-)-5-oxo-3-phenylhexanoate 

Relevant academic research and scientific papers

Enantioselective Michael addition of malonates to 2-enoylpyridine N-oxides catalyzed by chiral bisoxazoline-Zn(II) complex

An enantioselective Michael addition of malonates to 2-enoylpyridine N-oxides catalyzed by a chiral bisoxazoline-Zn(II) complex has been developed. The corresponding Michael adducts have been obtained in high yields with up to 96% ee. A plausible transiti

Enantioselective Michael reaction of ketone lithium enolates using a chiral ligand

The enantioselective Michael reaction of ketone lithium enolates using a chiral amine ligand (1) was studied. Michael adducts (4) of up to 94% ee were obtained by the reaction between methyl ketones (2) and Michael acceptors (3) having a benzylidene group.