enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 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). A specific example of an acyl chloride is acetyl chloride, CH 3 COCl. Acyl chlorides are the ...

  3. Tsuji–Wilkinson decarbonylation reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Wilkinson...

    The Tsuji–Wilkinson decarbonylation reaction is a method for the decarbonylation of aldehydes and some acyl chlorides. The reaction name recognizes Jirō Tsuji, whose team first reported the use of Wilkinson's catalyst (RhCl(PPh 3) 3) for these reactions: RC(O)X + RhCl(PPh 3) 3 → RX + RhCl(CO)(PPh 3) 2 + PPh 3

  4. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride is used for acetylation reactions, i.e., the introduction of an acetyl group. 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.

  5. Acyl halide - Wikipedia

    en.wikipedia.org/wiki/Acyl_halide

    The general formula for such an acyl halide can be written RCOX, where R may be, for example, an alkyl group, CO is the carbonyl group, and X represents the halide, such as chloride. Acyl chlorides are the most commonly encountered acyl halides, but acetyl iodide is the one produced (transiently

  6. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    Metal acyls also arise from reactions involving acyl chlorides with low-valence metal complexes or by the reaction of organolithium compounds with metal carbonyls. Metal acyls are often described by two resonance structures, one of which emphasizes the basicity of the oxygen center. O-alkylation of metal acyls gives Fischer carbene complexes. [10]

  7. Chloroacetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Chloroacetyl_chloride

    Chloroacetyl chloride is bifunctional—the acyl chloride easily forms esters [4] and amides, while the other end of the molecule is able to form other linkages, e.g. with amines. The use of chloroacetyl chloride in the synthesis of lidocaine is illustrative: [ 5 ]

  8. Rosenmund reduction - Wikipedia

    en.wikipedia.org/wiki/Rosenmund_reduction

    The Rosenmund reduction is a hydrogenation process in which an acyl chloride is selectively reduced to an aldehyde. The reaction was named after Karl Wilhelm Rosenmund, who first reported it in 1918. [1] The Rosenmund reduction. The reaction, a hydrogenolysis, is catalysed by palladium on barium sulfate, which is sometimes called the Rosenmund ...

  9. Category:Acyl chlorides - Wikipedia

    en.wikipedia.org/wiki/Category:Acyl_chlorides

    Pages in category "Acyl chlorides" The following 40 pages are in this category, out of 40 total. ... Trimellitic anhydride chloride This page was last ...