22169-72-8Relevant academic research and scientific papers
3,6-DIDEOXY-3,6-IMINO-1,2-O-ISODROPYLIDENE-α-D-GLUCOFURANOSE AS A DIVERGENT INTERMEDIATE FOR THE SYNTHESIS OF HYDROXYLATED PYRROLIDONES: SYNTHESIS IF 1,4-DIDEOXY-1,4-IMINO-L-GULITOL, 1,4-DIDEOXY-1,4-IMINO-D-LYXITOL, 2S,3S,4R,-3,4-DIHYDROXYPROLINE AND (1S,
Austin, Geoffrey N.,Baird, Peter D.,Fleet, George W. J.,Peach, Josephine M.,Smith, Paul W.,Watkin, David J.
, p. 3095 - 3108 (2007/10/02)
An efficient synthesis of the p-toluenesulphonate salt of 3,6-dideoxy-3,6-imino-1,2-O-isopropylidene-α-D-glucofuranose (1) from glucose is reported; the potential of (1) in making hydroxylated pyrrolidines is illustrated by the preparation of 1,4-dideoxy-
Synthesis of N-Acetyl Derivatives of (1R,5R)-6-Aza-2-oxabicyclooctan-3-one and (1S,5R,8R)-8-O-Benzyl-6-aza-2-oxabicyclooctan-3-one from D-Glucose
Gurjar, M. K.,Patil, V. J.,Pawar, S. M.
, p. 1115 - 1120 (2007/10/02)
N-Acetyl derivatives of (1R,5R)-6-aza-2-oxa-bicyclooctan-3-one (5) and (1S,5R,8R)-8-O-benzyl-6-aza-2-oxa-bicyclooctan-3-one (6), suitable chiral intermediates for (+)-retronecine (1) and (+)-crotanecine (2), have been synthesised from D-gluc
Digitoxigenin 3-O-β-D-Furanosides
Prisbe, Ernest J.,Verheyden, Julien P. H.,Montgomery, Wayne W.,Strosberg, Arthur M.
, p. 239 - 244 (2007/10/02)
The syntheses of the title compounds were accomplished by Koenig-Knorr condensation of acylated furanoses with digitoxigenin followed by basic hydrolysis of protecting groups.In this manner the riboside, 5-amino-5-deoxyriboside, 3,6-anhydroglucoside, and
