462647-76-3

Upstream product

• 621-84-1 O-benzyl carbamate 
• 768-03-6 Phenyl vinyl ketone 
• 733810-73-6 phenylmethyl 4-phenylhexahydropyridine-1-carboxylate 
• 501-53-1 benzyl chloroformate 
• 95798-23-5 1-(benzyloxycarbonyl)-4-hydroxypiperidine 
• 871926-94-2 3,4-dihydroxy-4-phenyl-piperidine-1-carboxylic acid benzyl ester 
• 886198-34-1 C₁₈H₁₇NO₄ 

Downstream Products

• 56296-78-7 Adofen 

Relevant academic research and scientific papers

Convenient synthesis of Cbz-protected β-amino ketones by a copper-catalysed conjugate addition reaction

A convenient synthesis of Cbz-protected β-amino ketones is reported. Benzyl carbamates and α,β-unsaturated ketones furnish the conjugate addition products in the presence of a Cu(II) catalyst under mild conditions. Other weakly basic nitrogen nucleophiles

CAN-mediated oxidative cleavage of 4-aryl-3,4-dihydroxypiperidines

A CAN-mediated oxidative cleavage of 4-aryl-3,4-dihydroxypiperidines 2Aa-Be to β-amino carbonyl compounds 3Aa-Be and 4Aa-Be in different ratios is described. This facile strategy was also used to synthesize racemic fluoxetine (5).