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  2. Indoline - Wikipedia

    en.wikipedia.org/wiki/Indoline

    The compound is based on the indole structure, but the 2-3 bond is saturated. By oxidation/dehydrogenation it can be converted to indole. [1] [2] Indoline can be produced from the reaction of indole, zinc and 85% phosphoric acid. [3] It was used to make Indocaine.

  3. Tabersonine - Wikipedia

    en.wikipedia.org/wiki/Tabersonine

    Tabersonine is a terpene indole alkaloid found in the medicinal plant Catharanthus roseus and also in the genus Voacanga [1] (both taxa belonging to the alkaloid-rich family Apocynaceae). Tabersonine is hydroxylated at the 16 position by the enzyme tabersonine 16-hydroxylase (T16H) to form 16-hydroxytabersonine . [ 2 ]

  4. Hagemann's ester - Wikipedia

    en.wikipedia.org/wiki/Hagemann's_ester

    Hagemann's ester, ethyl 2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many natural products including sterols , trisporic acids , and terpenoids .

  5. Dioxolane - Wikipedia

    en.wikipedia.org/wiki/Dioxolane

    It is related to tetrahydrofuran (THF) by replacement of the methylene group (CH 2) at the 2-position with an oxygen atom. The corresponding saturated 6-membered C 4 O 2 rings are called dioxanes. The isomeric 1,2-dioxolane (wherein the two oxygen centers are adjacent) is a peroxide. 1,3-dioxolane is used as a solvent and as a comonomer in ...

  6. Methylindole - Wikipedia

    en.wikipedia.org/wiki/Methylindole

    A variety of isomers of methyl indole derivatives are known: 1-methylindole; 2-methylindole; skatole (3-methylindole) 4-methylindole; 5-methylindole; 6-methylindole ...

  7. Proline-catalyzed aldol reactions - Wikipedia

    en.wikipedia.org/wiki/Proline-catalyzed_aldol...

    The Hajos–Parrish–Eder–Sauer–Wiechert and Barbas-List [1] reactions in organic chemistry are a family of proline-catalysed asymmetric aldol reactions.. In the 1970s, two research groups discovered (and published) almost simultaneously their discoveries of two related intramolecular reactions: Zoltan Hajos and David Parrish at Hoffmann-La Roche [2] [3] and Rudolf Wiechert et al at ...

  8. Structural scheduling of synthetic cannabinoids - Wikipedia

    en.wikipedia.org/wiki/Structural_scheduling_of...

    Naphthoylindoles: Any compound containing a 3-(1-naphthoyl)indole structure with substitution at the nitrogen atom of the indole ring by an alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or 2-(4-morpholinyl)ethyl group, whether or not further substituted in the indole ring to any extent and whether or not substituted in the naphthyl ring to any ...

  9. 5-Methylindole - Wikipedia

    en.wikipedia.org/wiki/5-Methylindole

    This page was last edited on 7 September 2022, at 20:40 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.