1321589-34-7

Basic information

• Product Name: (R)-tert-butyl 2-benzyloxymethyl-4-oxo-6-phenyl-3,4-dihydropyridine-1(2H)-carboxylate
• Synonyms: (R)-tert-butyl 2-benzyloxymethyl-4-oxo-6-phenyl-3,4-dihydropyridine-1(2H)-carboxylate
• CAS NO: 1321589-34-7
• Molecular Weight: 393.483
• Mol File: 1321589-34-7.mol

Chemical Properties

• CAS DataBase Reference: (R)-tert-butyl 2-benzyloxymethyl-4-oxo-6-phenyl-3,4-dihydropyridine-1(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-tert-butyl 2-benzyloxymethyl-4-oxo-6-phenyl-3,4-dihydropyridine-1(2H)-carboxylate(1321589-34-7)
• EPA Substance Registry System: (R)-tert-butyl 2-benzyloxymethyl-4-oxo-6-phenyl-3,4-dihydropyridine-1(2H)-carboxylate(1321589-34-7)

Safety Data

• Hazardous Substances Data: 1321589-34-7(Hazardous Substances Data)

Upstream product

• 193148-60-6 tert-butyl N-{(1S)-[(benzyloxy)methyl]-3-diazo-2-oxopropyl}carbamate 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 1321589-10-9 (R)-tert-butyl 1-(benzyloxymethyl)-3-oxo-5-phenylpent-4-ynylcarbamate 

Relevant articles and documents

Enantiospecific synthesis of pyridinones as versatile intermediates toward asymmetric piperidines

The enantiospecific syntheses of pyridinones from amino acids via a gold-catalyzed strategy are reported. Excellent stereocontrol was observed during the cyclization. This approach provides a straightforward tool for further synthetic applications toward