219313-07-2Relevant articles and documents
Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyco[3.1.1] heptanes: 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-D-mannopyranose
Yang, Guangbin,Kong, Fanzuo
, p. 77 - 83 (2007/10/03)
The title 1,3-anhydro sugar was synthesized from methyl α-D-glucopyranoside. The key intermediate for the synthesis was 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranosyl chloride (11) which was transformed into the target compound by ring closure with potassium tert-butoxide. Copyright (C) 1998 Elsevier Science Ltd.
SYNTHESIS OF A DI-AND A TRI-SACCHARIDE RELATED TO THE K-ANTIGEN OF Klebsiella TYPE 10 AND A STUDY OF THEIR INHIBITION IN THE PRECIPITIN REACTION
Sarkar, Arun K.,Ray, Asim K.,Roy, Nirmolendu
, p. 181 - 190 (2007/10/02)
Synthesis of methyl 3-O-α--galactopyranosyl-α--mannopyranoside (10) and methyl 3-O-α--galactopyranosyl-2-O-(β--glucopyranosyluronic acid)-α--mannopyranoside (11) in good yield are described.Both 10 and 11 significantly inhibit antigen-antib