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  2. Glycolaldehyde - Wikipedia

    en.wikipedia.org/wiki/Glycolaldehyde

    Glycolaldehyde then is converted to glyceraldehyde, presumably via initial tautomerization. [10] The presence of this glycolaldehyde in this reaction demonstrates how it might play an important role in the formation of the chemical building blocks of life. Nucleotides, for example, rely on the formose reaction to attain its sugar unit ...

  3. Formose reaction - Wikipedia

    en.wikipedia.org/wiki/Formose_reaction

    The formose reaction is of importance to the question of the origin of life, as it leads from simple formaldehyde to complex sugars like ribose, a building block of RNA.In one experiment simulating early Earth conditions, pentoses formed from mixtures of formaldehyde, glyceraldehyde, and borate minerals such as colemanite (Ca 2 B 6 O 11 5H 2 O) or kernite (Na 2 B 4 O 7). [6]

  4. Blue bottle experiment - Wikipedia

    en.wikipedia.org/wiki/Blue_bottle_experiment

    The chemical reactions and mechanism in the blue bottle experiment rely on the oxidation of a sugar with the aid of air and a redox dye in a basic solution. Other variations of this reaction have been reported that use four families of redox dyes: thiazines , oxazines , azines , and indigo carmine have all been reported to work with glucose and ...

  5. IRAS 16293−2422 - Wikipedia

    en.wikipedia.org/wiki/IRAS_16293%E2%88%922422

    Astronomers using the ALMA array found glycolaldehyde — a simple form of sugar — in the gas surrounding the star. [ 3 ] [ 4 ] This discovery was the first time sugar has been found in space around a solar-type star on scales corresponding to the distance between Sun and Uranus - i.e., the scales where a planet-forming disk is expected to arise.

  6. Glyceraldehyde - Wikipedia

    en.wikipedia.org/wiki/Glyceraldehyde

    The stereochemical configuration can only be determined from the chemical structure, whereas the optical rotation can only be determined empirically (by experiment). It was by a lucky guess that the molecular D-geometry was assigned to (+)-glyceraldehyde in the late 19th century, as confirmed by X-ray crystallography in 1951. [5]

  7. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Glycol cleavage is a specific type of organic chemistry oxidation. The carbon–carbon bond in a vicinal diol (glycol) is cleaved and instead the two oxygen atoms become double-bonded to their respective carbon atoms. Depending on the substitution pattern in the diol, these carbonyls will be ketones and/or aldehydes. [1]

  8. N-linked glycosylation - Wikipedia

    en.wikipedia.org/wiki/N-linked_glycosylation

    The different types of lipid-linked oligosaccharide (LLO) precursor produced in different organisms.. N-linked glycosylation is the attachment of an oligosaccharide, a carbohydrate consisting of several sugar molecules, sometimes also referred to as glycan, to a nitrogen atom (the amide nitrogen of an asparagine (Asn) residue of a protein), in a process called N-glycosylation, studied in ...

  9. 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.