265996-32-5

Basic information

• Product Name: (4S,5S)-N-(tert-butyloxycarbonyl)-5-ethenyl-4-phenylmethyl oxazolidin-2-one
• Synonyms: (4S,5S)-N-(tert-butyloxycarbonyl)-5-ethenyl-4-phenylmethyl oxazolidin-2-one
• CAS NO: 265996-32-5
• Molecular Weight: 303.358
• Mol File: 265996-32-5.mol

Chemical Properties

• CAS DataBase Reference: (4S,5S)-N-(tert-butyloxycarbonyl)-5-ethenyl-4-phenylmethyl oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-N-(tert-butyloxycarbonyl)-5-ethenyl-4-phenylmethyl oxazolidin-2-one(265996-32-5)
• EPA Substance Registry System: (4S,5S)-N-(tert-butyloxycarbonyl)-5-ethenyl-4-phenylmethyl oxazolidin-2-one(265996-32-5)

Safety Data

• Hazardous Substances Data: 265996-32-5(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 99113-28-7 (3S,4S)-5-[(tert-butoxycarbonyl)amino]-3-hydroxy-5-phenyl-1-pentene 
• 265996-19-8 (4S,5RS)-5-ethenyl-4-phenylmethyloxazolidin-2-one 

Downstream Products

• 482374-28-7 tert-butyl (2E)-3-[(4S,5S)-4-benzyl-N-(tert-butoxycarbonyl)-2-oxo-1,3-oxazolidin-5-yl]prop-2-enoate 

Relevant articles and documents

Regio- and stereoselective ring-opening of chiral 1,3-oxazolidin-2-one derivatives by organocopper reagents provides novel access to di-, tri- and tetra-substituted alkene dipeptide isosteres

Organocopper-mediated alkylation of β-(N-Boc-2-oxo-1,3-oxazolidin-5-yl)-α,β-enoates has been intensively investigated. Alkylation proceeded regio- and stereoselectively by anti-SN2′ ring-opening to provide a new route to the synthesis of Ψ[(E)-