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  2. 1,3-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,3-Cyclohexanedione

    1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones. It is a colorless compound that occurs ...

  3. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  4. Glutaric acid - Wikipedia

    en.wikipedia.org/wiki/Glutaric_acid

    1,5-Pentanediol, a common plasticizer and precursor to polyesters is manufactured by hydrogenation of glutaric acid and its derivatives. [3] Glutaric acid itself has been used in the production of polymers such as polyester polyols, polyamides. The odd number of carbon atoms (i.e. 5) is useful in decreasing polymer elasticity. [4]

  5. Cyclohexane-1,3-dione hydrolase - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,3-dione...

    In enzymology, a cyclohexane-1,3-dione hydrolase (EC 3.7.1.10) is an enzyme that catalyzes the chemical reaction cyclohexane-1,3-dione + H 2 O ⇌ {\displaystyle \rightleftharpoons } 5-oxohexanoate Thus, the two substrates of this enzyme are cyclohexane-1,3-dione and H 2 O , whereas its product is 5-oxohexanoate .

  6. Wieland–Miescher ketone - Wikipedia

    en.wikipedia.org/wiki/Wieland–Miescher_ketone

    The original Wieland–Miescher ketone is racemic and prepared in a Robinson annulation of 2-methyl-1,3-cyclohexanedione and methyl vinyl ketone. The intermediate alcohol is not isolated. An enantioselective synthesis employs L-proline as an organocatalyst: [7] This reaction was reported in 1971 by Z. G. Hajos and D. R. Parrish.

  7. Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedione

    1,2-Cyclohexanedione; 1,3-Cyclohexanedione; 1,4-Cyclohexanedione This page was last edited on 23 June 2017, at 01:22 (UTC). Text is available under the Creative ...

  8. Evans–Tishchenko reaction - Wikipedia

    en.wikipedia.org/wiki/Evans–Tishchenko_reaction

    The Evans–Tishchenko reaction is the diastereoselective reduction of β-hydroxy ketones to the corresponding 1,3-anti diol monoesters. The reaction employs a Lewis acid, often samarium iodide, and an aldehyde. It was first described in 1990 by David A. Evans and Amir Hoveyda, as a development of the well-known Tishchenko reaction discovered ...

  9. Cyclohexa-1,3-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,3-diene

    Cyclohexa-1,3-diene is an organic compound with the formula (C 2 H 4)(CH) 4. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Its refractive index is 1.475 (20 °C, D).