950777-59-0

Upstream product

• 950777-51-2 methyl (E)-3-[allyl(4-methylbenzenesulfonyl)amino]acrylate 
• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 

Downstream Products

• 950777-95-4 N-allyl-N-{(E)-3-[(3-triisopropylsilylprop-2-ynyl)oxy]prop-1-enyl}-4-methylbenzenesulfonamide 
• 1029537-68-5 N-allyl-N-{(E)-3-[2-((3aR,8aS)-2,2-dimethyl-8,8a-dihydro-3aH-indeno[1,2-d]oxazol-3-yl)-2-oxoethoxy]propenyl}-4-methylbenzenesulfonamide 
• 1428946-20-6 N-allyl-N-(ethoxy(oxiran-2-yl)methyl)-p-toluenesulfonamide 
• 1300117-49-0 N-allyl-N-{(E)-3-[(prop-2-ynyl)oxy]prop-1-enyl}-4-methylbenzenesulfonamide 
• 1029537-82-3 methyl (2S,3R)-3-[allyl(toluene-4-sulfonyl)amino]-2-hydroxypent-4-enoate 
• 1029537-76-5 N-allyl-N-{(R)-1-[(S)-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 
• 1300117-51-4 N-allyl-N-{(E)-3-[(3-trimethylsilylprop-2-ynyl)oxy]prop-1-enyl}-4-methylbenzene-sulfonamide 

Relevant academic research and scientific papers

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.