17296-10-5Relevant academic research and scientific papers
Studies of the stereoselective reduction of 2-hydroxyimino- hexopyranosides: LiBH4-Me3SiCl, a mild reducing agent of oximes to amines
Banaszek,Karpiesiuk
, p. 233 - 242 (2007/10/02)
Reduction of the title compounds of types 1 and 2 under mild conditions using LiBH4-Me3SiCl species, followed by acetylation, yielded the corresponding 2-amino sugars of α-D-gluco (5) and β D-manno (6) configuration, respectively, wi
Circular Dichroic Studies of 2-Amino-2-deoxy-galactopyranosides - Conformations of the 2-(N-Acetyl-p-bromobenzamido) Group
Lo, Lee-Chiang,Berova, Nina,Nakanishi, Koji,Morales, Ezequiel Q.,Vazquez, Jesus T.
, p. 321 - 330 (2007/10/02)
The CD spectra of methyl 2-amino-2-deoxy-D-galactopyranoside mono-N-acylates (acetyl or p-bromobenzoyl) resemble those of the corresponding O-acylates and can be accounted for by the additivity rule.However, the CD of pyranosides containing the N-acetyl-p-bromobenzamido imide group (NAcBz) are far more complex than those of mono-N-acylates and their O-counterparts, and furthermore, the solvent- and temperature-dependent changes differ for the α- and β-anomers.These differences can be accounted for by the different conformations of the 2-NAcBz group.
