475077-61-3

Basic information

• Product Name: (3S,αR,1'S,α'R)-tert-butyl 3-(N-benzyloxycarbonyl-N-α-methylbenzylamino)-3-[4-(3'-iso-propoxy-3'-oxo-1'-(N-benzyl-N-α-methylbenzylamino)propyl)phenyl]propanoate
• CAS NO: 475077-61-3
• Molecular Weight: 783.02
• Mol File: 475077-61-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,αR,1'S,α'R)-tert-butyl 3-(N-benzyloxycarbonyl-N-α-methylbenzylamino)-3-[4-(3'-iso-propoxy-3'-oxo-1'-(N-benzyl-N-α-methylbenzylamino)propyl)phenyl]propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,αR,1'S,α'R)-tert-butyl 3-(N-benzyloxycarbonyl-N-α-methylbenzylamino)-3-[4-(3'-iso-propoxy-3'-oxo-1'-(N-benzyl-N-α-methylbenzylamino)propyl)phenyl]propanoate(475077-61-3)
• EPA Substance Registry System: (3S,αR,1'S,α'R)-tert-butyl 3-(N-benzyloxycarbonyl-N-α-methylbenzylamino)-3-[4-(3'-iso-propoxy-3'-oxo-1'-(N-benzyl-N-α-methylbenzylamino)propyl)phenyl]propanoate(475077-61-3)

Safety Data

• Hazardous Substances Data: 475077-61-3(Hazardous Substances Data)

Upstream product

• 3459-92-5 DBC 
• 126275-19-2 (R)-N-allyl (1-phenylethyl)amine 

Relevant articles and documents

Asymmetric synthesis of homochiral differentially protected bis-β-amino acid scaffolds

A strategy for the asymmetric synthesis of homochiral [(R,R)- or (S,S)-], or meso-(R,S) bis-β-amino acid scaffolds, formally resulting from the stepwise conjugate addition of two differentially protected homochiral lithium amides to two α,β-unsaturated esters attached to a central arene, is demonstrated. Further manipulation enables the efficient synthesis of orthogonally protected pseudo-meso or pseudo-C2 symmetric scaffolds via selective N-benzyl or N-allyl deprotection, enabling regio-, stereo- and chemoselective functionalisation.