127000-08-2Relevant academic research and scientific papers
Improved synthesis of the Kijanimicin oligodeoxytetrasaccharide
Thiem, Joachim,Sajus, Henry
, p. 19 - 27 (2018/11/10)
By sequential synthesis the four 2,6-dideoxy saccharide moieties of the kijanimicin tetrasaccharide could be stereoselectively assembled. For formation of all required 2-deoxy α-glycoside linkages various S-(hexopyranosyl)-phosphorodithioates as donor str
Selective acylation of 6-deoxyglycals.
Horton,Priebe,Varela
, p. 317 - 324 (2007/10/02)
L-Rhamnal was acylated under a variety of conditions with various acylating reagents. Substitution of the hydroxyl group in the allylic position was favored when acetyl chloride, N-acetylimidazole, benzoyl chloride, and N-benzoylimidazole were used (40-60% net yields), whereas the homoallylic group of L-rhamnal was selectively protected when acetic anhydride-pyridine was employed for the acylation. The monoacetates of L-fucal underwent O-3----O-4 migration of the acetyl group, and selective acylation of this glycal could not be achieved.
