77874-38-5Relevant academic research and scientific papers
Differential O-3/O-4 regioselectivity in the glycosylation of α and β anomers of 6-O-substituted N-dimethylmaleoyl-protected d-glucosamine acceptors
Bohn, Maria L.,Colombo, Maria I.,Pisano, Pablo L.,Stortz, Carlos A.,Ruveda, Edmundo A.
, p. 2522 - 2536 (2008/03/27)
An assessment of the relative O-3/O-4 reactivities of both methyl α- and β-d-glycosides of N-dimethylmaleoyl (DMM) d-glucosamine acceptors protected at O-6 with benzoyl (Bz), benzyl (Bn), and tert-butyldiphenylsilyl (TBDPS) groups is presented using per-O
SYNTHESIS OF GALACTOFURANOSE DISACCHARIDES OF BIOLOGICAL SIGNIFICANCE
Marino, Carla,Varela, Oscar,Lederkremer, Rosa M. De
, p. 65 - 76 (2007/10/02)
Methyl β-D-galactofuranoside (3) was readily obtained by tin(IV) chloride-catalyzed glycosylation of penta-O-benzoyl-α,β-D-galactofuranose (1), followed by debenzoylation with sodium methoxide.Glycosylation of 1 with 2,3,5-tri-O-benzoyl-D-galactono-1,4-la
