823181-80-2Relevant academic research and scientific papers
Stereoselective access to the versatile 4-aminohex-5-ene-1,2,3-triol pattern
Ayad, Tahar,Faugeroux, Vanessa,Genisson, Yves,Andre, Chantal,Baltas, Michel,Gorrichon, Liliane
, p. 8775 - 8779 (2004)
We developed a stereocontrolled route allowing potential access to the eight isomers of 4-benzyl-aminohex-5-ene-1,2,3-triol in two or four steps and ca. 50% yield from readily available chiral nonracemic cis- or trans-α,β-epoxyimine precursors. A new (NH
