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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 naturally. It is the substrate for cyclohexanedione hydrolase. The compound exists mainly as the enol tautomer. [2]

  3. File:1,3-cyclohexanedione.png - Wikipedia

    en.wikipedia.org/wiki/File:1,3-cyclohexanedione.png

    What links here; Upload file; Special pages; Printable version; Page information; Get shortened URL; Download QR code

  4. 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.

  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. Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedione

    Download as PDF; Printable version; In other projects Wikidata item; ... 1,3-Cyclohexanedione; 1,4-Cyclohexanedione This page was last edited on 23 June ...

  7. Dicarbonyl - Wikipedia

    en.wikipedia.org/wiki/Dicarbonyl

    General structure of 1,2-, 1,3-, and 1,4-dicarbonyls. In organic chemistry, a dicarbonyl is a molecule containing two carbonyl (C=O) groups.Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4 ...

  8. Robinson annulation - Wikipedia

    en.wikipedia.org/wiki/Robinson_annulation

    The Wichterle reaction is a variant of the Robinson annulation that replaces methyl vinyl ketone with 1,3-dichloro-cis-2-butene. This gives an example of using a different Michael acceptor from the typical α,β-unsaturated ketone. The 1,3-dichloro-cis-2-butene is employed to avoid undesirable polymerization or condensation during the Michael ...

  9. Wieland–Miescher ketone - Wikipedia

    en.wikipedia.org/wiki/Wieland–Miescher_ketone

    The Wieland–Miescher ketone [2] is a racemic bicyclic diketone (enedione) and is a versatile synthon which has so far been employed in the total synthesis of more than 50 natural products, predominantly sesquiterpenoids, diterpenes and steroids possessing possible biological properties including anticancer, antimicrobial, antiviral, antineurodegenerative and immunomodulatory activities.