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  2. Haworth projection - Wikipedia

    en.wikipedia.org/wiki/Haworth_projection

    In chemistry, a Haworth projection is a common way of writing a structural formula to represent the cyclic structure of monosaccharides with a simple three-dimensional perspective. Haworth projection approximate the shapes of the actual molecules better for furanoses —which are in reality nearly planar—than for pyranoses that exist in ...

  3. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    The conventional numbering of the carbons in the closed form is the same as in the open-chain form. If the sugar is an aldohexose, with the carbonyl in position 1, the reaction may involve the hydroxyl on carbon 4 or carbon 5, creating a hemiacetal with five- or six-membered ring, respectively.

  4. Norman Haworth - Wikipedia

    en.wikipedia.org/wiki/Norman_Haworth

    Sir Walter Norman Haworth FRS [1] (19 March 1883 [2] – 19 March 1950) was a British chemist best known for his groundbreaking work on ascorbic acid while working at the University of Birmingham. He received the 1937 Nobel Prize in Chemistry "for his investigations on carbohydrates and vitamin C".

  5. Psicose - Wikipedia

    en.wikipedia.org/wiki/Psicose

    Haworth projection of D-psicose. Allulose, also known by its systematic name D-ribo-2-hexulose as well as by the name D-psicose, is a monosaccharide and a ketohexose. [2] [11] It is a C3 epimer of fructose. [2]

  6. Anomer - Wikipedia

    en.wikipedia.org/wiki/Anomer

    However, in order for anomers to exist, the sugar must be in its cyclic form, since in open-chain form, the anomeric carbon atom is planar and thus achiral. More formally stated, then, an anomer is an epimer at the hemiacetal/hemiketal carbon atom in a cyclic saccharide. [1] Anomerization is the process of conversion of one anomer to the other.

  7. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    Haworth Projection of β-D-glucopyranose Hermann Emil Fischer won the Nobel Prize in Chemistry (1902) for his work in determining the structure of the D - aldohexoses . [ 1 ] However, the linear, free-aldehyde structures that Fischer proposed represent a very minor percentage of the forms that hexose sugars adopt in solution.

  8. File:Beta-D-Glucopyranose.svg - Wikipedia

    en.wikipedia.org/wiki/File:Beta-D-Glucopyranose.svg

    Deutsch: Struktur von beta-D-Glucopyranose (Haworth-Schreibweise) English: Structure of beta-D-glucopyranose (Haworth projection);pl: Struktura beta-D-glukozy (projekcja Hawortha) Date

  9. N-Acetylglucosamine - Wikipedia

    en.wikipedia.org/wiki/N-Acetylglucosamine

    GlcNAc is the monomeric unit of the polymer chitin, which forms the exoskeletons of arthropods like insects and crustaceans. It is the main component of the radulas of mollusks, the beaks of cephalopods, and a major component of the cell walls of most fungi. Polymerized with glucuronic acid, it forms hyaluronan.

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