34366-99-9Relevant academic research and scientific papers
Molecular recognition XI. The synthesis of extensively deoxygenated derivatives of the H-type 2 human blood group determinant and their binding by an anti-H-type 2 monoclonal antibody and the lectin 1 of Ulex europaeus
Spohr, Ulrike,Paszkiewicz-Hnatiw, Eugenia,Morishima, Naohiko,Lemieux, Raymond U.
, p. 254 - 271 (2007/10/02)
The relative potencies of a wide variety of deoxygenated derivatives of the methyl glycoside of α-L-Fuc-(1->2)-β-D-Gal-(1->4)-β-D-GlcNAc (the H-type 2 human blood related trisaccharide) for the inhibition of the binding of an artificial H-type 2 antigen b
Synthesis of some trideoxy-D-hexoses and derivatives thereof from D-glucono-1,5-lactone
Regeling,Chittenden
, p. 79 - 91 (2007/10/02)
Enantiospecific syntheses of methyl 2,3,4-trideoxy-α-D- and β-D-glycero-hexopyranoside (10 and 11), methyl α-D- and β-D-amicetopyranoside (24 and 25), (2S)-1,2-hexanediol (36), (2S)-1,2,6-hexanetriol (37), and some derivatives thereof from D-glucono-1,5-lactone are described. Enantiospecific syntheses of methyl 2,3,4-trideoxy-α-D- and -β-D-glycero-hexopyranoside (10 and 11), methyl α-D- and β-D-amicetopyranoside (24 and 25), (2S)-1,2-hexanediol (36), (2S)-1,2,6-hexanetriol (37), and some derivatives thereof from D-glucono-1,5-lactone are described.
