24190-11-2

Upstream product

• 3966-30-1 (R)-Atrolactic acid 
• 7472-67-5 α-phenyl-α-methoxypropanoic acid 
• 3558-61-0 methyl 2-methoxy-2-phenylacetate 
• 4358-87-6 (RS)-methyl mandelate 
• 24190-08-7 (R)-(-)-2-methoxy-2-phenylpropionic acid 
• 149-73-5 trimethyl orthoformate 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 

Downstream Products

• 832688-52-5 (R)-3⁽⁵⁾-(1-methoxy-1-phenyl-ethyl)-5⁽³⁾-methyl-1H-pyrazole 
• 832688-55-8 (R)-2-chloro-6-[3-(1-methoxy-1-phenylethyl)-5-methylpyrazol-1-yl]pyridine 
• 832688-57-0 (R)-2-[3-(1-methoxy-1-phenylethyl)-5-methylpyrazol-1-yl]pyridine-1-oxide 
• 832688-51-4 (R)-5-methoxy-5-phenylhexane-2,4-dione 
• 24190-12-3 (-)-1,1,2-Trimethyl-2-methoxy-2-phenyl-propanol-1 
• 84999-97-3 C₂₃H₃₀O₂ 
• 84999-98-4 C₂₂H₂₈O₂ 
• 84999-96-2 C₂₁H₂₆O₂ 
• 84999-99-5 C₂₂H₂₆O₂ 
• 84999-95-1 (2R)-2-methoxy-2-phenylpropyl (Z)-3-phenyl-1-butenyl ether 
• 84999-94-0 (R)-(-)-cinnamyl 2-methoxy-2-phenylpropyl ether 
• 69160-04-9 (R)-2-Methoxy-2-phenyl-propan-1-ol 

Relevant academic research and scientific papers

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

A NEW AND EFFECTIVE ASYMMETRIC SYNTHESIS OF 3-PHENYLALKANALS

Highly optically active 3-phenylalkanals were obtained by the reaction of alkyl halides and a chiral homoenolate equivalent derived from the cinnamyl ether 3 and potassium diisopropylamide, followed by acidic hydrolysis.