869720-69-4

Basic information

• Product Name: (S)-((2R,3R)-1-Benzyl-3-methoxy-4-oxo-azetidin-2-yl)-(tert-butyl-dimethyl-silanyloxy)-acetaldehyde
• Synonyms: (S)-((2R,3R)-1-Benzyl-3-methoxy-4-oxo-azetidin-2-yl)-(tert-butyl-dimethyl-silanyloxy)-acetaldehyde
• CAS NO: 869720-69-4
• Molecular Weight: 363.529
• Mol File: 869720-69-4.mol

Chemical Properties

• CAS DataBase Reference: (S)-((2R,3R)-1-Benzyl-3-methoxy-4-oxo-azetidin-2-yl)-(tert-butyl-dimethyl-silanyloxy)-acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-((2R,3R)-1-Benzyl-3-methoxy-4-oxo-azetidin-2-yl)-(tert-butyl-dimethyl-silanyloxy)-acetaldehyde(869720-69-4)
• EPA Substance Registry System: (S)-((2R,3R)-1-Benzyl-3-methoxy-4-oxo-azetidin-2-yl)-(tert-butyl-dimethyl-silanyloxy)-acetaldehyde(869720-69-4)

Safety Data

• Hazardous Substances Data: 869720-69-4(Hazardous Substances Data)

Relevant articles and documents

Diastereoselectivity enhancement in the 1,3-cycloaddition of β-lactam aldehydes. Application to the synthesis of enantiopure indolizidinone amino esters

Enantiopure α-alkoxy β-lactam acetaldehydes were prepared via the thiazole-based one-carbon homologation. The 1,3-dipolar cycloaddition reaction involving α-alkoxy β-lactam acetaldehyde-derived azomethine ylides gave with excellent diastereoselectivity hi