220934-05-4

Upstream product

• 100-52-7 benzaldehyde 
• 68003-55-4 (E)-N-allylbenzylideneimine 

Downstream Products

• 118673-21-5 2-[(3R,4S)-2-Oxo-4-phenyl-1-((E)-propenyl)-azetidin-3-yl]-isoindole-1,3-dione 
• 99398-27-3 cis,cis-2-phenyl-4-(benzyloxy)-5-methylpiperidine 
• 2032-33-9 N-benzyl-N-propylamine 
• 99398-30-8 all-cis-1-phenyl-4-methyl-10-hydroxy-2-azadecalin 
• 99398-25-1 Benzyl-((2S,3R,4R,5R)-3,5-dimethyl-2-phenyl-piperidin-4-yl)-amine 
• 118673-19-1 cis-3-Phenoxy-4-phenyl-1-(1'-propenyl)-2-azetidinone 
• 99398-29-5 all-cis-1-phenyl-4-methyl-2-aza-5-oxadecalin 
• 99398-24-0 2-phenyl-4-(benzylamino)-3,5-dimethylpiperidine 
• 118673-20-4 3,3-Dimethyl-4-phenyl-1-((E)-propenyl)-azetidin-2-one 
• 99398-32-0 trans,trans,cis-2-phenyl-3,5-dimethyl-4-(benzyloxy)piperidine 
• 99398-31-9 trans,cis,trans-2-phenyl-3,5-dimethyl-4-(benzyloxy)piperidine 
• 99398-26-2 cis,cis-2-phenyl-4-n-butoxy-5-methylpiperidine 
• 99398-34-2 1-phenyl-4-methyl-9-morpholino-2-azaindan 
• 99398-33-1 1-phenyl-4-methyl-9-morpholino-2-azaindan 

Relevant academic research and scientific papers

Stereocontrolled Synthesis of N-Vinyl-, N-(1'-Propenyl)-, and N-Unsubstituted-β-lactams from 2-Aza-1,3-butadienes via the Staudinger Reaction

2-Aza-1,3-butadienes 2 and 5 were synthesized in good yields and on a large scale.Reaction of 2 and 5 with acid chlorides in the presence of triethylamine (Staudinger reaction) resulted in the high-yielding formation of N-vinyl- and N-(1'-propenyl)-β-lact

2-AZA-1,3-DIENES AS NOVEL PRECURSORS FOR THE SYNTHESIS OF N-UNSUBSTITUTED β-LACTAMS. A THREE STEP SYNTHESIS OF 4-ACETOXY-3-PHENOXY-2-AZETIDINONE

2-Aza-1,3-dienes, prepared in excellent yields from aldehydes and readily available allylamine, were utilized to synthesize N-(1-propenyl)-β-lactams.Oxidative cleavage of the N-protecting group produced N-unsubstituted β-lactams. 4-Acetoxy-3-phenoxy-2-aze