Monosaccharides projection formulae

Filamin 370 Filaria worms 24 Fimbriae 6. See also Pili Fingerprinting. See also Peptide mapping of DNA 259 of proteins 118, 360 First Law of Thermodynamics 282 First order reactions 457 Fischer, Edmond H. 84 Fischer, Emil H. 42, 83 Fischer projection formula 42 of monosaccharides 163 FK506 488 Flagella... 

Two sugars can link to each other by losing water from OHs to form disaccharides. Figure 4.6 shows the Haworth projection formulas of four important disaccharides sucrose, lactose, maltose, and cellobiose, which all have the same molecular formulas, C12H22011. Sucrose and lactose are the most abundant and most important disaccharides of natural origin. Maltose and cellobiose are repeating units of polymeric starch and cellulose, respectively. Disaccharides may hydrolyze to form two monosaccharide molecules. 

Draw the Fischer projection formula for a simple monosaccharide. 

The Haworth projection formulas are neater ways of writing the ring forms shown in the equilibria above and yet preserving the configuration shown at each chiral carbon. It is not difficult to translate the open-chain structure for a monosaccharide into the Haworth ring structure. 

Do not rotate a Fischer projection formula in the plane of the page, because you might inadvertently convert a compound into its enantiomer. When using Fischer projections it is usually best to convert them to structures with wedges and dashes, and then manipulate them. Although a Fischer projection formula can be used for the stereogenic center in any compound, it is most commonly used for monosaccharides. 

CONFORMATIONAL STRUCTURES Although Haworth projection formulas are often used to represent carbohydrate structure, they are oversimplifications. Bond angle analysis and X-ray analysis demonstrate that conformational formulas are more accurate representations of monosaccharide structure (Figure 7.10). Conformational structures are more accurate because they illustrate the puckered nature of sugar rings. 

Terms in bold are defined glycoconjugate 238 monosaccharide 238 oligosaccharide 238 disaccharide 238 polysaccharide 238 aldose 239 ketose 239 Fischer projection formulas 240 epimers 240... 

Chirality in Monosaccharides Fischer Projection Formulas and o,L-Sugars... 

CYCLIC MONOSACCHARIDES HEMIACETALS AND HEMIKETALS Haworth Projection Formulas... 

The Fischer projection is a convenient way of showing the configurations of the linear forms of monosaccharides. This convention depicts the concepts of stereochemistry established by Jacobus Henricus van t Hoff and Joseph Achille Le Bel in a simplified form. While these abbreviated structural formulas are simple to write and easy to visualize, there are some guidelines that should be taken into account when converting a three-dimensional structure into a Fischer projection and in its manipulation (Fig. 1.2) ... 

Drawing the Haworth Projection of a Monosaccharide from the Structural Formula... 

Figure 4.1 shows the formulas and names for D-aldoses using simplified Fischer projections. The occurrence of aldoses of importance in food is compiled in Table 4.1. Epimers are monosaccharides which differ in configuration at only one chiral C-atom. D-Glucose and D-mannose are 2-epimers. D-glucose and D-galactose are 4-epimers. 

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