409095-60-9Relevant articles and documents
A stereocontrolled synthesis of 3-acetamido-1,3,5-trideoxy- and 1,3,5,6-tetradeoxy-1,5-imino-d-glucitol
Simak, Ondrej,Stanek, Jan,Moravcova, Jitka
experimental part, p. 966 - 971 (2009/09/05)
3-Acetamido-5-amino-3,5,6-trideoxy-d-glucono-1,5-lactam and 3-acetamido-5-amino-3,5-dideoxy-d-glucono-1,5-lactam were synthesized from corresponding 3-acetamido-3-deoxy-β-d-glucopyranosides in 63% and 35% overall yield, respectively. Acetylation followed by reduction led to the title 3-acetamido-3-deoxy derivatives of both deoxynojirimycin and 1,6-dideoxynojirimycin. The procedure developed is useful for a multi-gram scale.
Synthesis of methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-formyl-α-d- erythro-hex-2-enopyranoside
Mangione, María I.,Suárez, Alejandra G.,Spanevello, Rolando A.
, p. 149 - 153 (2007/10/03)
The synthesis of the title compound was achieved in seven steps and 61% overall yield from methyl α-d-glucopyranoside.
Synthesis of methyl 3,6-diacetamido-2,3,4,6-tetradeoxy-α-L-threo-hexopyranoside, an intermediate in the synthesis of the antibiotic negamycin
Streicher, Wolfgang,Reinshagen, Hellmuth
, p. 383 - 388 (2007/10/02)
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