120966-32-7Relevant academic research and scientific papers
Redox Glycosidation: Stereoselective Syntheses of 1 -> 6 Linked Disaccharides via Thionoester Intermediates
Barrett, Anthony G. M.,Lee, Albert C.
, p. 2818 - 2824 (2007/10/02)
Perbenzyl derivatives of the disaccharides benzyl 6-O-(α(and β)-D-glucopyranosyl)-α-D-galactopyranoside and benzyl 6-O-(α(and β)-D-mannopyranosyl)-α-D-galactopyranoside were each prepared in a stereoselective manner by acylation, thionation, and reductive
Redox Glycosidation via Thionoester Intermediates
Barrett, Anthony G.M.,Bezuidenhoudt, Barend C.B.,Howell, Amy R.,Lee, Albert C.,Russell, Mark A.
, p. 2275 - 2277 (2007/10/02)
Several steroidal glycosides were prepared via esterification with aldonic acids, Lawesson thionation, lithium triethylborohydride mediated reductive methylation, and silver(I)-catalyzed ring closure.
