874287-52-2

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 299216-13-0 (S)-3-amino-4-benzyl-1,3-oxazolan-2-one 

Downstream Products

• 669081-31-6 N-[1-(3,4-dimethoxyphenyl)but-3-enyl]-2,2,2-trifluoroacetamide 
• 669081-33-8 (S)-1-(3,4-dimethoxyphenyl)but-3-enylamine 
• 874287-74-8 7-((S)-1-(3,4-dimethoxyphenyl)but-3-enylamino)hept-1-en-3-yl methyl carbonate 
• 874287-55-5 (S)-N-[1-(3,4-dimethoxyphenyl)but-3-enyl]benzamide 
• 669081-21-4 (4S,1'S)-3-(1'-(3,4-dimethoxyphenyl)but-3'-enylamino)-4-phenylmethyloxazolidin-2-one 

Relevant academic research and scientific papers

Dual activation in asymmetric allylsilane addition to chiral N-acylhydrazones: Method development, mechanistic studies, and elaboration of homoallylic amine adducts

Chiral N-acylhydrazones derived from commercially available 4-benzyl-2-oxazolidinone provide a rigid, conformationally restricted template to impart facial selectivity in additions to C=N bonds. In the presence of indium(III) trifluoromethanesulfonate [In