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  2. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    In chemistry, the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection. Fischer projections were originally proposed for the depiction of carbohydrates and used by chemists, particularly in organic chemistry and biochemistry .

  3. Galactose - Wikipedia

    en.wikipedia.org/wiki/Galactose

    The main pathway of galactose metabolism is the Leloir pathway; humans and other species, however, have been noted to contain several alternate pathways, such as the De Ley Doudoroff Pathway. The Leloir pathway consists of the latter stage of a two-part process that converts β-D-galactose to UDP-glucose. The initial stage is the conversion of ...

  4. File:DGalactose Fischer.svg - Wikipedia

    en.wikipedia.org/wiki/File:DGalactose_Fischer.svg

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  5. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    Of these D-isomers, all except D-altrose occur in living organisms, but only three are common: D-glucose, D-galactose, and D-mannose. The L -isomers are generally absent in living organisms; however, L -altrose has been isolated from strains of the bacterium Butyrivibrio fibrisolvens .

  6. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    The Fischer projection is a systematic way of drawing the skeletal formula of an open-chain monosaccharide so that each stereoisomer is uniquely identified. Two isomers whose molecules are mirror-images of each other are identified by prefixes ' D-' or ' L-', according to the handedness of the chiral carbon atom that is farthest from the carbonyl.

  7. Emil Fischer - Wikipedia

    en.wikipedia.org/wiki/Emil_Fischer

    Hermann Emil Louis Fischer FRS FRSE FCS (German pronunciation: [ˈeːmiːl ˈfɪʃɐ] ⓘ; 9 October 1852 – 15 July 1919) was a German chemist and 1902 recipient of the Nobel Prize in Chemistry. He discovered the Fischer esterification. He also developed the Fischer projection, a symbolic way of drawing asymmetric carbon atoms. He also ...

  8. Stereochemistry - Wikipedia

    en.wikipedia.org/wiki/Stereochemistry

    A Fischer projection is a simplified way to depict the stereochemistry around a stereocenter. ... Example: D-glucose and D-galactose are epimers, ...

  9. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    A Fischer projection can be used to differentiate between L- and D- molecules Chirality (chemistry). For instance, by definition, in a Fischer projection the penultimate carbon of D-sugars are depicted with hydrogen on the left and hydroxyl on the right. L-sugars will be shown with the hydrogen on the right and the hydroxyl on the left.