134340-66-2

Upstream product

• 135822-87-6 (E)-N-(furan-2-ylmethylene)-4-methylbenzenesulfonamide 
• 920-36-5 (2-methylpropyl)lithium 
• 13707-47-6 2-furaldehyde tosylimine 
• 4104-47-6 N-sulfinyl-p-toluenesulfonamide 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 134340-72-0 (R)-6-Hydroxy-2-isobutyl-1-(toluene-4-sulfonyl)-1,6-dihydro-2H-pyridin-3-one 
• 158568-78-6 N-((R)-1-Furan-2-yl-3-methyl-butyl)-4-methyl-benzenesulfonamide 
• 134452-31-6 (S)-N-tosyl-α'-isobutyl-α-furfuryl amine 
• 134340-72-0 C₁₆H₂₁NO₄S 
• 944063-45-0 C₁₇H₂₃NO₄S 
• 1220-80-0 (S)-4-methyl-2-(toluene-4-sulfonamido)pentanoic acid 

Relevant academic research and scientific papers

Synthesis of 2-aza-1-cyano-4-hydroxyanthraquinones

Phthalide annulation of 2-alkylpyridin-3-ones results in the formation of the unexpected 2-aza-1-cyano-4-hydroxy-anthraquinones, the cyano moiety originating from the 3-cyanophthalide. These compounds hold great potential against Epstein-Barr Virus Early

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