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  2. Glycolaldehyde - Wikipedia

    en.wikipedia.org/wiki/Glycolaldehyde

    Glycolaldehyde is the second most abundant compound formed when preparing pyrolysis oil (up to 10% by weight). [8] Glycolaldehyde can be synthesized by the oxidation of ethylene glycol using hydrogen peroxide in the presence of iron(II) sulfate. [9]

  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. 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.

  5. Blue bottle experiment - Wikipedia

    en.wikipedia.org/wiki/Blue_bottle_experiment

    For instance, glucose would be oxidized to gluconate by oxygen. [12] However, the experiment also works with compounds such as vitamin C and benzoin, which do not contain an aldehyde group. [4] Thus, the reaction is actually the oxidation of an acyloin or related α-hydroxy carbonyl group, which is a structural feature of glucose, to a 1,2 ...

  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. Glycosylation - Wikipedia

    en.wikipedia.org/wiki/Glycosylation

    Glycosylation is the reaction in which a carbohydrate (or 'glycan'), i.e. a glycosyl donor, is attached to a hydroxyl or other functional group of another molecule (a glycosyl acceptor) in order to form a glycoconjugate.

  8. O-linked glycosylation - Wikipedia

    en.wikipedia.org/wiki/O-linked_glycosylation

    O-linked glycosylation is the attachment of a sugar molecule to the oxygen atom of serine (Ser) or threonine (Thr) residues in a protein. O-glycosylation is a post-translational modification that occurs after the protein has been synthesised.

  9. 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 ...