Galactopyranose 0-

Fig. 9. Partial structural formulas and shorthand notations for principal hemiceUuloses found in wood, where the sugar units ate noted as P-D-xylopyranose (Xylp), 4-Omethyl-a-D-glucopyranosyluronic acid (GlupU), a-L-arabinofuranose (Araf), P-D-glucopyranose (Glup), P-D-mannopyranose (Manp), and P-D-galactopyranose (Galp) for (a) arabino-4-O-methylglucuronoxylan from softwood, (b) 0-acetyl-galactoglucomannan from softwood, and...

Galactose differs from glucose in configuration at C-4. The C-4 hydroxyl is axial in p-D-galactopyranose, but it is equatorial in p-o-glucopyranose. ... 

From the rearrangement of tetra-O-acetyl-2-hydroxy-D-galactal in boiling acetic acid it was possible to isolate l,2,4,6-tetra-0-acetyl-2,3-dide-h.ydro-3-deoxy-a-jy-threo-hexose (32) (58%) and a small amount of 1,2,3,4,6-penta-O-acetyl-jS-D-galactopyranose. In the reaction mixture the presence of some a-pentaacetate was demonstrated chromatographically but NMR spectroscopy indicated no resonances corresponding to the / anomer of compound 32. These spectral measurements indicate that compound 32 constituted 80% of the mixture of products. 

The only recorded example using this method in the sugar series is the chlorination of l,2 3,4-di-0-isopropylidene-D-galactopyranose (73) which affords in addition to the expected 6-chloro-6-deoxy derivative 74a, a 5,6-unsaturated derivative 75 as well. These products were separated by silica gel column chromatography no yields were given. 

Problem 25,13 Draw /3-o-galactopyranose and jS-D-mannopyranose in their more stable chair conformations. Label each ring substituent as either axial or equatorial. Which would you expect to be more stable, galactose or mannose ... 

Draw /3-t-galactopyranose in its more stable chair conformation, and label the substituents as either axial or equatorial. 

Deoxy-p-D-xy/o-hexopyranose 2-Deoxy-D-ribo-hexose not 2-deoxy-D-allose not 4-deoxy-p-D-galactopyranose... 

Epimerization of 4 at C-2 provided 5a-carba-a-DL-galactopyranose (6). When the pentaacetate IS was heated in acetic acid containing sulfuric acid, epimerization occurred at C-2 through an intermediary cyclic acetoxonium ion (18), with anchimeric assistance of the vicinal, axial acetoxyl group. After acetylation, 5a-carba-a-DL-galactopyranose pentaacetate (19) was obtained in a yield of 14% it was converted into 6 by hydrolysis. The antimicrobial activity of the racemate 6 was found to be about half that of the natural antibiotic 7 in the same assay system, indicating that the L-antipode is probably inactive. " ... 

When carba-a-DL-galactopyranose (6) reacts with a, a-dimethoxy-toluene, there are obtained two stereoisomers, 69 and 70, whose structures... 

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