1311201-63-4

Upstream product

• 5703-57-1 3-phenylpent-4-enoic acid 
• 78-09-1 orthocarbonic acid tetraethyl ester 
• 774-48-1 (diethoxymethyl)benzene 
• 60066-61-7 ethyl 3-phenyl-4-pentenoate 
• 105-57-7 diethyl acetal 
• 122-51-0 orthoformic acid triethyl ester 
• 78-39-7 Triethyl orthoacetate 
• 137586-02-8 3-Phenyl-pent-4-enoyl chloride 
• 100-46-9 benzylamine 
• 104-54-1 3-Phenylpropenol 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 64-17-5 ethanol 
• 1311201-49-6 (5S)-2,2-dimethyl-5-(1-phenylallyl)-1,3-dioxane-4,6-dione 

Downstream Products

• 1311201-65-6 C₂₉H₃₁Cl₂NO₅S 
• 392655-86-6 (3R)-3-phenyl-1-pent-4-en-1-ol 
• 62624-45-7 (S)-4-phenyl-1-tosylpyrrolidin-2-one 
• 1431854-78-2 C₁₂H₁₆O₃ 
• 1431854-80-6 C₁₃H₁₈O₅S 
• 1431854-82-8 C₁₂H₁₅N₃O₂ 
• 1431854-83-9 C₁₂H₁₇NO₂ 
• 52950-37-5 4-amino-(3S)-3-phenyl-butyric acid hydrochloride 

Relevant academic research and scientific papers

Dynamic Kinetic Resolution of 3-Aryl-4-pentenoic Acids

The first example of dynamic kinetic resolution (DKR) of chiral unsaturated carboxylic acids is described. The application of tandem metal-enzyme DKR is a powerful tool for the manufacture of high-value chemical commodities. This new protocol of kinetic r

Studies on the chemoenzymatic synthesis of 3-phenyl-GABA and 4-phenyl-pyrrolid-2-one: The influence of donor of the alkoxy group on enantioselective esterification

A new chemoenzymatic method for the synthesis of enantiomerically pure 3-phenyl-γ-aminobutyric acid 1 and 4-phenyl-pyrrolid-2-one 9 based on the enzymatic kinetic resolution of 3-phenyl-4-pentenoic acid 2 is described herein. Enzymatic resolution of the r

The studies on chemoenzymatic synthesis of Femoxetine

The studies on enzymatic kinetic resolution of 3-phenyl-4-pentenoic acid esters were performed. The obtained results demonstrated that the careful choice of biocatalyst and a reaction type are very important for successful enzymatic kinetic resolution. Ki

A chiral bidentate sp2-N ligand, naph-diPIM: Application to CpRu-catalyzed asymmetric dehydrative C-, N-, and O-allylation

A handy new ligand: The CpRu complex (Cp=cyclopentadienyl) of a new type of chiral bisamidine ligand with a naphtho[1,2-b:7,8-b]dipyrroloimidazole (Naph-diPIM) skeleton with a Bronsted acid efficiently catalyzes dehydrative intermolecular C-allylation with high enantio- and regioselectivity. The catalytic system also gives nearly enantiomerically pure cycloalkanes and N- and O-heterocycles with a substrate/catalyst ratios of up to 10 000.