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  2. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    In chemistry, an acyl group is a moiety derived by the removal of one or more hydroxyl groups from an oxoacid, [1] including inorganic acids. It contains a double-bonded oxygen atom and an organyl group ( R−C=O ) or hydrogen in the case of formyl group ( H−C=O ).

  3. Acyl-CoA synthetase - Wikipedia

    en.wikipedia.org/wiki/Acyl-CoA_synthetase

    Acyl-CoA synthetases, also known as acyl-CoA ligases, are enzymes that “activate” fatty acids by thioesterification to CoA. [1] It represents the initial step of fatty acid metabolism so that fatty acids can participate in catabolic and anabolic pathways. [ 1 ]

  4. Transition metal acyl complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_acyl...

    Acyl complexes are usually low-spin and spin-paired. Monometallic acyl complexes adopt one of two related structures, C-bonded and η 2-C-O-bonded. These forms sometimes interconvert. For the purpose of electron-counting, C-bonded acyl ligands count as 1-electron ligands, akin to pseudohalides. η 2-Acyl ligands count as 3-electron "L-X" ligands.

  5. Acylation - Wikipedia

    en.wikipedia.org/wiki/Acylation

    In chemistry, acylation is a broad class of chemical reactions in which an acyl group (R−C=O) is added to a substrate. The compound providing the acyl group is called the acylating agent. The substrate to be acylated and the product include the following: alcohols, esters; amines, amides; arenes or alkenes, [1] ketones

  6. Acyl halide - Wikipedia

    en.wikipedia.org/wiki/Acyl_halide

    Acyl halides are rather reactive compounds often synthesized to be used as intermediates in the synthesis of other organic compounds. For example, an acyl halide can react with: water, to form a carboxylic acid. This hydrolysis is the most heavily exploited reaction for acyl halides as it occurs in the industrial synthesis of acetic acid.

  7. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl , where R is a side chain . They are reactive derivatives of carboxylic acids ( R−C(=O)OH ).

  8. N-Acylamides - Wikipedia

    en.wikipedia.org/wiki/N-Acylamides

    N-acyl amides are a general class of endogenous fatty acid compounds characterized by a fatty acyl group linked to a primary amine metabolite by an amide bond. Broadly speaking, N-acyl amides fall into several categories: amino acid conjugates (e.g., N-arachidonoyl-glycine), neurotransmitter conjugates (e.g., N-arachidonoyl-serotonin), ethanolamine conjugates (e.g., anandamide), and taurine ...

  9. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl is an acyl group having the formula −C(=O)−CH 3. For further information on the types of chemical reactions compounds such as acetyl chloride can undergo, see acyl halide . Two major classes of acetylations include esterification and the Friedel-Crafts reaction .