134452-30-5

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 135822-87-6 (E)-N-(furan-2-ylmethylene)-4-methylbenzenesulfonamide 
• 4104-47-6 N-sulfinyl-p-toluenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 
• 193755-27-0 (1R,2S)-2-((S)-1-Furan-2-yl-pentylamino)-1,2-diphenyl-ethanol 
• 193755-24-7 (1R,2S)-2-{[1-Furan-2-yl-meth-(E)-ylidene]-amino}-1,2-diphenyl-ethanol 
• 98-01-1 furfural 
• 134340-65-1 N-(1-(furan-2-yl)pentyl)-4-methylbenzenesulfonamide 
• 109-72-8 n-butyllithium 

Downstream Products

• 134340-71-9 (S)-2-Butyl-6-hydroxy-1-(toluene-4-sulfonyl)-1,6-dihydro-2H-pyridin-3-one 

Relevant academic research and scientific papers

A new synthesis of chiral α-substituted furfuryl amines by diastereoselective addition of organometallic reagents

A new method to prepare chiral α-substituted furfuryl amines was achieved in high d.e. values and chemical yields.

An efficient preparation of optically active α-furfuryl amide by kinetic resolution using the modified Sharpless asymmetric epoxidation reagents

Kinetic resolution of α-furfuryl amide was first carried out by using the modified Sharpless asymmetric epoxidation reagent to give the slow-reacting enantiomers, (S)-1(a-h) and (R)-1(b,f) in high enantioselectivity (90-100% e.e) and high chemical yield (

An efficient preparation of optically active α-furfuryl amide by kinetic resolution using the modified sharpless asymmetric epoxidation reagent

Kinetic resolution of α-furfuryl amide was first carried out by using the modified Sharpless asymmetric epoxidation reagent to give the slow-reacting enantiomers, (S)-la-f and (R)-lb,f in high enantioselectivity (90-100% e.e) and high chemical yield (45-5