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  2. 2-Pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/2-Pyrrolidone

    2-Pyrrolidone, also known as 2-pyrrolidinone or butyrolactam, is an organic compound consisting of a 5-membered lactam, making it the simplest γ-lactam. It is a colorless liquid that is miscible with water and most common organic solvents.

  3. Pyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine

    Pyrrolidine, also known as tetrahydropyrrole, is an organic compound with the molecular formula (CH 2) 4 NH. It is a cyclic secondary amine , also classified as a saturated heterocycle . It is a colourless liquid that is miscible with water and most organic solvents.

  4. Phosphoribosyl-N-formylglycineamide - Wikipedia

    en.wikipedia.org/wiki/Phosphoribosyl-N-formylgly...

    [1] [2] The vitamins thiamine [3] and cobalamin [4] also contain fragments derived from FGAR. [5] FGAR is formed when the enzyme phosphoribosylglycinamide formyltransferase adds a formyl group from 10-formyltetrahydrofolate to glycineamide ribonucleotide (GAR) in reaction EC 2.1.2.2: [6] GAR + 10-formyltetrahydrofolate → FGAR + tetrahydrofolate

  5. N-Vinylpyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Vinylpyrrolidone

    N-Vinylpyrrolidone (NVP) is an organic compound consisting of a 5-membered lactam ring linked to a (2 carbon) vinyl group. It is a colorless liquid although commercial samples can appear yellowish. It is produced industrially by vinylation of 2-pyrrolidone, i.e. the base-catalyzed reaction with acetylene. [2]

  6. Formylation - Wikipedia

    en.wikipedia.org/wiki/Formylation

    The first GAR transformylase inhibitor Lometrexol [(6R)5,10-dideazatetrahydrofolate] was developed in the 1980s through a collaboration between Eli Lilly and academic laboratories. [20] Although similar in structure to N10-formyl-THF, lometrexol is incapable of carrying out one carbon transfer reactions. [19]

  7. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    The Hantzsch pyrrole synthesis is the reaction of β-ketoesters (1) with ammonia (or primary amines) and α-haloketones (2) to give substituted pyrroles (3). [ 13 ] [ 14 ] The Hantzsch pyrrole synthesis

  8. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    The oxidation products derived from methyl are hydroxymethyl group −CH 2 OH, formyl group −CHO, and carboxyl group −COOH. For example, permanganate often converts a methyl group to a carboxyl (−COOH) group, e.g. the conversion of toluene to benzoic acid. Ultimately oxidation of methyl groups gives protons and carbon dioxide, as seen in ...

  9. Category:Pyrrolidones - Wikipedia

    en.wikipedia.org/wiki/Category:Pyrrolidones

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