904848-89-1

Basic information

• Product Name: (E)-(R)-N-[(3S)-2,3-diphenylbut-1-enyl]-4-methyloxazolidin-2-one
• Synonyms: (E)-(R)-N-[(3S)-2,3-diphenylbut-1-enyl]-4-methyloxazolidin-2-one
• CAS NO: 904848-89-1
• Molecular Weight: 307.392
• Mol File: 904848-89-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-(R)-N-[(3S)-2,3-diphenylbut-1-enyl]-4-methyloxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-(R)-N-[(3S)-2,3-diphenylbut-1-enyl]-4-methyloxazolidin-2-one(904848-89-1)
• EPA Substance Registry System: (E)-(R)-N-[(3S)-2,3-diphenylbut-1-enyl]-4-methyloxazolidin-2-one(904848-89-1)

Safety Data

• Hazardous Substances Data: 904848-89-1(Hazardous Substances Data)

Upstream product

• 1201351-64-5 (R)-N-(trimethylsilylmethyl)-4-methyloxazolidin-2-one 
• 2042-85-5 1,2-diphenylpropan-1-one 
• 457602-58-3 methyl β-phenyl-α-phenylbutyrate 
• 101-41-7 benzeneacetic acid methyl ester 
• 585-71-7 (1-bromoethyl)benzne 
• 108774-24-9 2,3-diphenyl-1-butanol 
• 4042-43-7 (4R)-4-methyl-1,3-oxazolidin-2-one 
• 457602-59-4 2,3-diphenylbutyraldehyde 

Downstream Products

• 457602-65-2 (4R,3'S,4'S,1''S)-4-methyl-3-[4'-phenyl-4'-(1''-phenylethyl)[1',2']dioxetan-3'-yl]oxazolidin-2-one 

Relevant articles and documents

Isolation and syn elimination of a peterson adduct to obtain optically pure product in the diastereoselective synthesis of oxazolidinone-functionalized enecarbamates

The Peterson reaction of (4R)-N-(trimethylsilyl)methyl-4-alkyloxazolidin-2- one gives (E/Z)-(4R)-N-(2', 3'- diphenylbut-1'-enyl)-4-alkyloxazolidin-2-ones (enecarbamates) with increasing (Z)-selectivity and moderate-to-high diastereoselectivity in the indi

Highly diastereoselective dioxetane formation in the photooxygenation of enecarbamates with an oxazolidinone chiral auxiliary: Steric control in the [2 + 2] cycloaddition of singlet oxygen through conformational alignment

The photooxygenation of oxazolidinone-substituted enecarbamates leads to diastereomerically pure dioxetanes. The high diastereoselectivity is rationalized in terms of effective π-facial control achieved by shielding one side of the double bond with the ch