1350971-27-5

Basic information

• Product Name: (2R,3R)-tert-butyl 3-(3-chlorophenyl)-2-(diphenylmethyleneamino)-4-nitrobutanoate
• CAS NO: 1350971-27-5
• Molecular Weight: 478.975
• Mol File: 1350971-27-5.mol

Chemical Properties

• CAS DataBase Reference: (2R,3R)-tert-butyl 3-(3-chlorophenyl)-2-(diphenylmethyleneamino)-4-nitrobutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-tert-butyl 3-(3-chlorophenyl)-2-(diphenylmethyleneamino)-4-nitrobutanoate(1350971-27-5)
• EPA Substance Registry System: (2R,3R)-tert-butyl 3-(3-chlorophenyl)-2-(diphenylmethyleneamino)-4-nitrobutanoate(1350971-27-5)

Safety Data

• Hazardous Substances Data: 1350971-27-5(Hazardous Substances Data)

Upstream product

• 3156-35-2 3-chloro-β-nitrostyrene 
• 81477-94-3 N-(diphenylmethylene)glycine tert-butyl ester 

Relevant articles and documents

Stereodivergency in catalytic asymmetric conjugate addition reactions of glycine (Ket)imines

Stereodivergent catalytic asymmetric conjugate reactions of glycine (ket)imines with nitroalkenes have been achieved using various chiral catalyst systems derived from a multidentate amino alcohol (1). The stepwise nature of the [3 + 2] cycloaddition reactions of N-metalated azomethine ylides has also been demonstrated by highly enantio- and diastereoselective syntheses of exo-5 and endo-8 from the respective syn-4 and anti-7 conjugate addition products in a one-pot tandem fashion.