950777-52-3

Upstream product

• 54879-64-0 N-[(4-methoxyphenyl)methyl]-4-methylbenzenesulfonamide 
• 292638-85-8 acrylic acid methyl ester 
• 922-67-8 propynoic acid methyl ester 

Downstream Products

• 950777-60-3 N-((E)-3-hydroxyprop-1-enyl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide 
• 1029537-80-1 methyl (2S,3R)-2-hydroxy-3-[(4-methoxybenzyl)(4-methylbenzenesulfonyl)amino]pent-4-enoate 
• 1300117-19-4 N-(4-methoxybenzyl)-N-{(1S)-1-[(1S)-2-((3aR,8aS)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-1-hydroxy-2-oxo-ethyl]allyl}-4-methylbenzenesulfonamide 
• 1029537-74-3 N-(4-methoxybenzyl)-N-{(1R)-1-[(1S)-2-((3aR,8aS)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-1-hydroxy-2-oxoethyl]allyl}-4-methylbenzenesulfonamide 
• 1300117-50-3 N-(4-methoxybenzyl)-N-{(E)-3-[(3-trimethylsilylprop-2-ynyl)oxy]prop-1-enyl}-4-methylbenzenesulfonamide 
• 1300117-48-9 N-(4-methoxybenzyl)-N-{(E)-3-[(prop-2-ynyl)oxy]prop-1-enyl}-4-methylbenzenesulfonamide 
• 1029537-66-3 N-(4-methoxybenzyl)-N-{(E)-3-[2-((3aR,8aS)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-oxoethoxy]propen-1-yl}-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Aza-Wacker-type reaction between electron-deficient olefins and N-alkylsulfonamides

A palladium-catalyzed oxidative amination protocol of electron-deficient olefins by aza-Wacker-type reaction with N-alkylsulfonamides was developed. The presence of the stoichiometric amount of methanesulfonic acid was crucial for the success of this tran

Synthesis of 1,2-amino alcohols by sigmatropic rearrangements of 3-(N-Tosylamino)allylic alcohol derivatives

Sigmatropic rearrangements of 3-(N-tosylamino)allylic alcohol derivatives, a particular subclass of functionalized enamides, have been investigated. Whereas the presence of the nitrogen atom alters the stereochemical outcome of Ireland-Claisen rearrangeme

Stereoselective synthesis of 1,2-aminoalcohols by [2,3]-wittig rearrangements

[2,3]-Wittig rearrangements of (E)-3-aza-allylic alcohol derivatives can provide access to functionalized 1,2-aminoalcohols with high syn or anti diastereoselectivity depending on the anionic stabilizing group (amide or alkyne). American Chemical Society.