4458-60-0

Upstream product

• 100-52-7 benzaldehyde 
• 84370-56-9 trans-3,5-dimethyl-1,1-dioxo-2-phenyl-4-thiazolidinone 
• 84370-51-4 trans-3,5-dimethyl-2-phenyl-4-thiazolidinone 
• 84370-52-5 cis-3,5-dimethyl-2-phenyl-4-thiazolidinone 
• 84370-50-3 5-methyl-2-phenyl-4-thiazolidinone 
• 89578-44-9 (S)-(+)-N-Propionyl-N-methylamphetamine 
• 622-29-7 N-Benzylidenemethylamine 
• 89578-42-7 (S)-(+)-1-Propionyl-2-ethylpiperidine 
• 84370-55-8 cis-3,5-dimethyl-1,1-dioxo-2-phenyl-4-thiazolidinone 
• 67-63-0 isopropyl alcohol 

Relevant academic research and scientific papers

Diastereoface-Differentiating Synthesis of Substituted β-Lactams from Chiral Imines and/or Chiral α-Chloro Iminium Chlorides

Reaction of imines carrying a chiral substituent at a nitrogen atom with symmetric or prochiral α-chloro iminium chlorides leads in a diastereoface-differentiating reaction to a mixture of diatereoisomeric or epimeric β-lactams.Attempts were made to determine the absolute configuration of obtained chiral β-lactams.Reaction of prochiral imines with chiral α-chloro iminium chlorides also provides mixtures of diastereomeric β-lactams or their enantiomers with a clear selectivity.