109055-08-5Relevant academic research and scientific papers
Facile Preparation of 1,6-Anhydro-2-azido-3-O-benzyl-2-deoxy-β-D-glucopyranose and Its 4-O-Substituted Derivatives
Sakairi, Nobuo,Takahashi, Shunya,Wang, Feng,Ueno, Yoshihito,Kuzuhara, Hiroyoshi
, p. 1756 - 1758 (2007/10/02)
Treatment of 1,6-anhydro-2,3-O-endo-benzylidene-β-D-mannopyranose derivatives with trimethylamine-borane (1/1)-aluminium chloride resulted in highly regioselective fission of the cyclic acetals to give the corresponding 2-O-unprotected-3-O-benzyl derivatives. Trifluoromethane-sulfonylation of these, followed by nucleophilic substitution, afforded 2-azido-2-deoxy derivatives in good yields.
APPLICATION OF VICINAL CARBON-PROTON COUPLING CONSTANTS TO THE CONFORMATIONAL ANALYSIS OF BENZYLIDENE-TYPE ACETALS OF 1,6-ANHYDRO-β-D-HEXOPYRANOSES
Cano, Felix H.,Foces-Foces, Concha,Barbero-Jimenez, Jesus,Bernabe, Manuel,Martin-Lomas, Manuel
, p. 1 - 10 (2007/10/02)
(13)C-N.m.r. chemical shifts and 3JC,H values have been used to investigate the conformation of dioxolane-type acetals of 1,6-anhydro-β-D-hexopyranoses.The crystal structures of some of these compounds have been determined by X-ray d
