38345-65-2

Upstream product

• 2835-06-5 phenylglycin 
• 1578-63-8 d'acide 2-fluoro-2-phenyl acetique 
• 63818-94-0 (R)-α-fluoro-α-phenylacetic acid 

Downstream Products

• 128864-50-6 (R)-Fluoro-phenyl-acetic acid (S)-1,2-dimethyl-propyl ester 
• 128864-49-3 (R)-Fluoro-phenyl-acetic acid (R)-1,2-dimethyl-propyl ester 
• 133175-41-4 (R)-2-Fluoro-2-phenyl-N-((S)-1,2,2-trimethyl-propyl)-acetamide 
• 133175-25-4 (R)-2-Fluoro-2-phenyl-N-((R)-1,2,2-trimethyl-propyl)-acetamide 
• 128864-55-1 (R)-Fluoro-phenyl-acetic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester 
• 116046-10-7 (R)-Fluoro-phenyl-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 128864-58-4 (R)-Fluoro-phenyl-acetic acid (R)-2-methyl-1-phenyl-propyl ester 
• 128864-59-5 (R)-Fluoro-phenyl-acetic acid (S)-2-methyl-1-phenyl-propyl ester 
• 133175-54-9 (R)-2-Fluoro-N-[(S)-1-(4-methoxy-phenyl)-ethyl]-2-phenyl-acetamide 
• 133175-38-9 (R)-2-Fluoro-N-[(R)-1-(4-methoxy-phenyl)-ethyl]-2-phenyl-acetamide 
• 116046-15-2 (R)-Fluoro-phenyl-acetic acid (R)-2-(2-methoxy-phenoxy)-1-phenyl-ethyl ester 
• 133175-56-1 (R)-N-[(R)-(4-Bromo-phenyl)-phenyl-methyl]-2-fluoro-2-phenyl-acetamide 
• 133175-65-2 (R)-N-[(S)-(4-Bromo-phenyl)-phenyl-methyl]-2-fluoro-2-phenyl-acetamide 
• 133175-33-4 (R)-2-((R)-2-Fluoro-2-phenyl-acetylamino)-3-phenyl-propionic acid methyl ester 

Relevant academic research and scientific papers

1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazoles: Identification of a potent aurora kinase inhibitor with a favorable antitumor kinase inhibition profile

The optimization of a series of 5-phenylacetyl 1,4,5,6-tetrahydropyrrolo[3, 4-c]pyrazole derivatives toward the inhibition of Aurora kinases led to the identification of compound 9d. This is a potent inhibitor of Aurora kinases that also shows low nanomol

ACIDE 2-FLUORO-2-PHENYLACETIQUE. PARTIE 3. CORRELATION ENTRE LA CONFIGURATION DE SES AMIDES D'AMINES CHIRALES ET LES DEPLACEMENTS CHIMIQUES DU PROTON ET DU FLUOR

Proton and fluorine chemical shifts of amides from PhCHFCO2H (used as a chiral derivatizing agent) and amines L1CH(NH2)L2 are correlated with configuration in order to assign configuration of chiral amines by 19F NMR spectroscopy.