243980-62-3Relevant academic research and scientific papers
A novel carbocyclic ring closure of hex-5-enopyranosides and pent-4- enofuranosides
Gallos, John K.,Koftis, Theocharis V.,Koumbis, Alexandras E.,Moutsos, Vassilios I.
, p. 1289 - 1291 (1999)
Nitrile oxide cycloadditions to hex-5-enopyranosides and pent-4- enofuranosides give spiroisoxazolines, which upon reductive opening of the heterocyclic ring undergo spontaneous intramolecular aldol-like condensation to give six- and five-membered densely
Carbocyclic ring closure of hex-5-enopyranosides and pent-4-enofuranosides: A nitrile oxide approach
Gallos, John K.,Koftis, Theocharis V.
, p. 415 - 423 (2007/10/03)
A nitrile oxide approach on the carbocyclic ring closure of hex-5-enopyranosides and pent-4-enofuranosides was studied. The densely functionalised cyclopentane and cyclohexane derivatives were found suitable for the synthetic transformations. The N-O bond
