138665-01-7Relevant articles and documents
Synthesis of 3,6-dideoxy-D-erythro-hexos-4-ulose and identification as the 3,6-dideoxy-4-ketohexose from Pasteurella pseudotuberculosis.
Stevens,Schultze,Smith,Pillai,Rubenstein,Strominger
, p. 5767 - 5768 (1973)
-
Mannose-binding geometry of pradimicin A
Nakagawa, Yu,Doi, Takashi,Taketani, Takara,Takegoshi,Igarashi, Yasuhiro,Ito, Yukishige
, p. 10516 - 10525 (2013/08/23)
Pradimicins (PRMs) and benanomicins are the only family of non-peptidic natural products with lectin-like properties, that is, they recognize D-mannopyranoside (Man) in the presence of Ca2+ ions. Coupled with their unique Man binding ability, t
Novel and convenient method for the syntheses of 2,6-dideoxypyranoses, 3,6-dideoxypyranoses, and azido (amino) analogs of 3,6-dideoxypyranoses
Chang, Cheng-Wei Tom,Clark, Terri,Ngaara, Mumbi
, p. 6797 - 6801 (2007/10/03)
A novel method of regioselective deoxygenation of methyl 4,6-O-benzylidene-2,3-di-O-tosyl-α-D-glucopyranoside, and its application for the syntheses of 2,6-dideoxypyranoses, 3,6-dideoxypyranoses, and azido (amino) analogs of 3,6-dideoxypyranoses were reported.