925460-41-9

Upstream product

• 80885-30-9 (E)-4-(benzyloxy)-2-buten-1-ol 
• 57620-22-1 N-benzyl-2,4-dinitro-benzenesulfonamide 
• 100-46-9 benzylamine 
• 925460-37-3 (E)-N-benzyl-N-[4-(benzyloxy)but-2-enyl]-2,4-dinitro-benzenesulfonamide 

Downstream Products

• 861109-14-0 2-(N-benzyl-N-((E)-4-(benzyloxy)but-2-enyl)amino)-1-(pyrrolidin-1-yl)ethanone 
• 1401332-32-8 N-benzyl-2-(benzyl(hydroxy)amino)-4-(benzyloxy)butan-1-amine 

Relevant academic research and scientific papers

Lewis acid mediated asymmetric [2,3]-sigmatropic rearrangement of allylic amines. Scope and mechanistic investigation

(Chemical Equation Presented) The first asymmetric [2,3]-sigmatropic rearrangement of achiral allylic amines has been realized by quaternization of the amines with an enantiomerically pure diazaborolidine and subsequent treatment with Et3N. The

Ir-catalyzed allylic amination/ring-closing metathesis: A new route to enantioselective synthesis of cyclic β-amino alcohol derivatives

(Chemical Equation Presented) Ir-catalyzed allylic aminations of (E)-4-benzyloxy-2-butenyl methyl carbonate with benzylamine using Feringa's (Sa,Sc,Sc)- phosphoramidite as a chiral ligand afforded linear-aminated achiral p