950777-94-3

Upstream product

• 10285-80-0 N-tosyl-3-butenylamine 
• 950777-50-1 methyl (E)-3-[but-3-enyl(4-methylbenzenesulfonyl)amino]acrylate 
• 950777-57-8 N-(but-3-enyl)-N-((E)-3-hydroxyprop-1-enyl)-4-methylbenzenesulfonamide 
• 104465-98-7 (3-bromoprop-1-yn-1-yl)triisopropylsilane 

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.