128677-87-2

Basic information

• Product Name: (4S)-N-[(3S)-phenylbutanoyl]-4-phenylmethyl-1,3-oxazolidin-2-one
• Synonyms: (4S)-N-[(3S)-phenylbutanoyl]-4-phenylmethyl-1,3-oxazolidin-2-one
• CAS NO: 128677-87-2
• Molecular Weight: 323.392
• Mol File: 128677-87-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (4S)-N-[(3S)-phenylbutanoyl]-4-phenylmethyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-N-[(3S)-phenylbutanoyl]-4-phenylmethyl-1,3-oxazolidin-2-one(128677-87-2)
• EPA Substance Registry System: (4S)-N-[(3S)-phenylbutanoyl]-4-phenylmethyl-1,3-oxazolidin-2-one(128677-87-2)

Safety Data

• Hazardous Substances Data: 128677-87-2(Hazardous Substances Data)

Upstream product

• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 90719-30-5 (4S)-3-((E)-2-butenoyl)-4-benzyl-2-oxazolidinone 
• 98-80-6 phenylboronic acid 
• 772-14-5 (R)-3-phenylbutyric acid 
• 4593-90-2 (S)-2-phenylbutanoic acid 
• 102-92-1 Cinnamoyl chloride 
• 100-59-4 phenylmagnesium chloride 
• 591-51-5 phenyllithium 
• 128891-66-7 (4S)-4-benzyl-3-[(2E)-3-phenylprop-2-enoyl]-1,3-oxazolidin-2-one 
• 917-54-4 methyllithium 
• 100-58-3 phenylmagnesium bromide 
• 128677-85-0 C₁₅H₂₀O₃ 
• 40217-17-2 (R)-4-(phenylmethyl)-2-oxazolidinone 
• 1184-58-3 dimethylaluminum chloride 

Downstream Products

• 25488-26-0 erythro-D-(2R,3R)-β-methylphenylalanine 
• 25488-27-1 threo-L-(2S,3R)-β-methylphenylalanine 
• 128677-94-1 (2S,3R)-2-azido-3-phenylbutanoic acid 
• 128677-92-9 (2R)-azido-(3R)-phenylbutanoic acid 
• 128677-91-8 (4S)-3-(2'R,3'R)-2'-azido-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone 
• 128707-88-0 (4R)-3-(2'S,3'R)-2'-azido-3'-(phenylbutanoyl)-4-(phenylmethyl)-2-oxazolidinone 
• 128677-93-0 (2R)-azido-(3S)-phenylbutanoic acid 
• 128677-95-2 (2S,3S)-2-azido-3-phenylbutanoic acid 
• 59905-30-5 threo-D-(2R,3S)-β-methylphenylalanine 
• 25488-25-9 (2S,3S)-methylphenylalanine 
• 143251-56-3 (R)-4-Benzyl-3-((2S,3R)-2-bromo-3-phenyl-butyryl)-oxazolidin-2-one 
• 143251-56-3 (S)-4-Benzyl-3-((2R,3R)-2-bromo-3-phenyl-butyryl)-oxazolidin-2-one 

Relevant articles and documents

Palladium-Catalyzed Diastereoselective Synthesis of 3-Arylbutanoic Acid Derivatives

The first palladium-catalyzed diastereoselective conjugate addition of arylboronic acids to chiral imides is reported. The catalytic system employing 4-tert-butyloxazolidin-2-one as the chiral auxiliary in a mixed solvent system of MeOH/H2O (1:3) under an air atmosphere provides the optically active 3-arylbutanoic acid derivatives in excellent yields with high diastereoselectivity.

Asymmetric conjugate additions of TMSI promoted monoorganocuprate reagents, Li[RCuI], to various N-enoyl oxazolidinones

Diastereoselective conjugate additions to different α,β-unsaturated N-acyl oxazolidinones using various monoorganocuprate reagents, Li[RCuI], are described. The TMSI activated conjugate addition reactions provided high yields (80-98%) and reversed major d

Stereoselective Conjugate Addition of Organoaluminum Chlorides to α,β-Unsaturated Carboxylic Acid Derivatives

Organoaluminum chlorides react smoothly with α,β-unsaturated N-acyloxazolidinones providing chiral β-branched carboxylic acid derivatives.An unexpected contrast between the mode of reaction of dimethylaluminum chloride and that of the higher homologues is observed.While diethylaluminum chloride and its higher homologues react with the acceptors at low temperature via a polar pathway, dimethylaluminum chloride requires activation by UV-light or radical initiation under otherwise identical conditions.With bicyclic oxazolidinones derived from galactosamine a high stereoselection is accomplished in the formation of the branched carboxylic acid derivative.