100058-89-7

Upstream product

• 515-30-0 2-phenyllactic acid 
• 74-88-4 methyl iodide 
• 3558-61-0 methyl 2-methoxy-2-phenylacetate 
• 20731-95-7 methyl 2-hydroxy-2-phenylpropanoate 
• 4358-87-6 (RS)-methyl mandelate 
• 108-86-1 bromobenzene 

Downstream Products

• 102751-76-8 2-methoxy-1,1,2-triphenyl-propan-1-ol 
• 31508-44-8 2-phenylpropionic acid methyl ester 
• 7472-67-5 α-phenyl-α-methoxypropanoic acid 
• 98324-55-1 (1R,3R,4S:R)-(-)-menthyl 2-methoxy-2-phenylpropionate 
• 832688-51-4 (R)-5-methoxy-5-phenylhexane-2,4-dione 
• 832688-57-0 (R)-2-[3-(1-methoxy-1-phenylethyl)-5-methylpyrazol-1-yl]pyridine-1-oxide 

Relevant academic research and scientific papers

Conformational analysis of MαNP esters, powerful chiral resolution and 1H NMR anisotropy tools - aromatic geometry and solvent effects on Δδ values

The MαNP acid method is very powerful for the preparation of enantiopure alcohols by resolution and the simultaneous determination of their absolute configurations by the 1H NMR anisotropy effect, where the syn-syn conformation is taken as the

Regioselective synthesis of optically active (pyrazolyl)pyridines with adjacent quaternary carbon stereocenter: Chiral N,N-donating ligands

Novel optically active 2-(pyrazol-1-yl)pyridines have been prepared using resolved the O-methyl ether of atrolactic acid as a source of the adjacent quaternary carbon stereocenter. Different regioisomers were formed selectively in the reaction of 2-hydraz