669081-33-8

Upstream product

• 669081-24-7 N-(4-benzyl-2-oxo-oxazolidin-3-yl)-N-[1-(3,4-dimethoxy-phenyl)-but-3-enyl]-2,2,2-trifluoro-acetamide 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 874287-52-2 (S)-3-(3,5-dimethoxybenzylidene)amino-4-phenylmethyl-2-oxazolidinone 
• 669081-31-6 N-[1-(3,4-dimethoxyphenyl)but-3-enyl]-2,2,2-trifluoroacetamide 

Downstream Products

• 1162664-73-4 C₁₇H₂₅NO₄ 
• 874287-74-8 7-((S)-1-(3,4-dimethoxyphenyl)but-3-enylamino)hept-1-en-3-yl methyl carbonate 

Relevant academic research and scientific papers

New entry to the asymmetric synthesis of (-)-lasubine I and (+)-subcosine I

A new synthetic entry to (-)-lasubine I and (+)-subcosine I has been established by employing the (S)-allylalkoxy benzylamine as a chiral synthon. The synthesis involves the formation of an α,β-unsaturated lactone by RCM reaction followed by an intramolec

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

Trifluoroacetyl-Activated Nitrogen-Nitrogen Bond Cleavage of Hydrazines by Samarium(II) Iodide

(Matrix presented) Trifluoroacetyl derivatives of hydrazines undergo clean and efficient reductive cleavage of the N-N bond with Sml2 in the presence of MeOH. After N-trifluoroacetylation, acyl-, aryl-, and alkyl-substituted hydrazines are redu