848862-09-9Relevant academic research and scientific papers
Synthesis of a trihydroxylated azepane from D-arabinose by way of an intramolecular alkene nitrone cycloaddition
Moutel, Stephane,Shipman, Michael,Martin, Olivier R.,Ikeda, Kyoko,Asano, Naoki
, p. 487 - 491 (2005)
The synthesis of 1,6-imino-1,5,6-trideoxy-l-xylo-hexitol, a trihydroxylated azepane, from d-arabinose was achieved by way of an intramolecular alkene nitrone cycloaddition. The final product as well as its bicyclic precursor, (3R,4S,5S)-3,4-dihydroxy-8-ox
