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  2. Talose - Wikipedia

    en.wikipedia.org/wiki/Talose

    Talose is an aldohexose sugar. It is an unnatural monosaccharide , that is soluble in water and slightly soluble in methanol . Some etymologists suggest that talose's name derives from the automaton of Greek mythology named Talos , but the relevance is unclear.

  3. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    The 2-ketohexoses psicose, fructose and tagatose occur naturally as the D-isomers, whereas sorbose occurs naturally as the L-isomer. D-Sorbose is commonly used in the commercial synthesis of ascorbic acid. [10] D-Tagatose is a rare natural ketohexose that is found in small quantities in food. [11]

  4. GDP-6-deoxy-D-talose 4-dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/GDP-6-deoxy-D-talose_4-de...

    The 3 substrates of this enzyme are GDP-6-deoxy-D-talose, NAD +, and NADP +, whereas its 4 products are GDP-4-dehydro-6-deoxy-D-mannose, NADH, NADPH, and H +. This enzyme belongs to the family of oxidoreductases , specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor.

  5. File:Infrared spectra of D-talose monobenzoate and related ...

    en.wikipedia.org/wiki/File:Infrared_spectra_of_D...

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  6. Psicose - Wikipedia

    en.wikipedia.org/wiki/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 ] Fructose can be converted to allulose by the enzymes D -tagatose 3-epimerase ( EC 5.1.3.31 ) and/or D -psicose 3-epimerase ( EC 5.1.3.30 ), which has allowed for ...

  7. Aldose - Wikipedia

    en.wikipedia.org/wiki/Aldose

    Fischer projection of D-glyceraldehyde. Like most carbohydrates, simple aldoses have the general chemical formula C n (H 2 O) n.Because formaldehyde (n=1) and glycolaldehyde (n=2) are not generally considered to be carbohydrates, [1] the simplest possible aldose is the triose glyceraldehyde, which only contains three carbon atoms.

  8. Kiliani–Fischer synthesis - Wikipedia

    en.wikipedia.org/wiki/Kiliani–Fischer_synthesis

    The Kiliani–Fischer synthesis, named for German chemists Heinrich Kiliani and Emil Fischer, is a method for synthesizing monosaccharides.It proceeds via synthesis and hydrolysis of a cyanohydrin, followed by reduction of the intermediate acid to the aldehyde, thus elongating the carbon chain of an aldose by one carbon atom while preserving stereochemistry on all the previously present chiral ...

  9. dTDP-6-deoxy-L-talose 4-dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/DTDP-6-deoxy-L-talose_4-de...

    Thus, the two substrates of this enzyme are dTDP-6-deoxy-L-talose and NADP +, whereas its 3 products are dTDP-4-dehydro-6-deoxy-L-mannose, NADPH, and H +. This enzyme belongs to the family of oxidoreductases , specifically those acting on the CH-OH group of donor with NAD + or NADP + as acceptor.