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  2. Vincoline - Wikipedia

    en.wikipedia.org/wiki/Vincoline

    Methyl (20S)-2-hydroxy-6,7-didehydro-3α,20-epoxy-2β,5α,12β,19α-aspidospermidine-3β-carboxylate Systematic IUPAC name Methyl (3a S ,3a 1 S ,4 S ,6 R ,6a S ,11b R )-6a-hydroxy-4-methyl-6a,7,12,13-tetrahydro-1 H ,3a 1 H ,4 H ,6 H -3a,6-methanoindolizino[1′,8′:4,5,6]oxepino[3,4- b ]indole-6-carboxylate

  3. Indoxacarb - Wikipedia

    en.wikipedia.org/wiki/Indoxacarb

    Indoxacarb is the active ingredient in a number of household insecticides, including cockroach and ant baits, and can remain active after digestion. [10] In 2012 DuPont's Professional Products including the line of Advion and Arilon products was purchased by Syngenta. [11]

  4. Majdine - Wikipedia

    en.wikipedia.org/wiki/Majdine

    This article about an alkaloid is a stub. You can help Wikipedia by expanding it.

  5. Indoline - Wikipedia

    en.wikipedia.org/wiki/Indoline

    Indoline is an aromatic heterocyclic organic compound with the chemical formulation C 8 H 9 N. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring.

  6. 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 .

  7. 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 ...

  8. β-Carboline - Wikipedia

    en.wikipedia.org/wiki/Β-Carboline

    β-Carboline (9H-pyrido[3,4-b]indole) represents the basic chemical structure for more than one hundred alkaloids and synthetic compounds. The effects of these substances depend on their respective substituent. Natural β-carbolines primarily influence brain functions but can also exhibit antioxidant [1] effects.

  9. Arecoline - Wikipedia

    en.wikipedia.org/wiki/Arecoline

    A double Mannich reaction between methylamine (1), acetaldehyde (2) and formaldehyde (3) in the presence of hydroxylamine hydrochloride is supposed to have delivered 1-methyl-1,2,5,6-tetrahydropyridine-3-carbaldehyde oxime hydrochloride (4) as the product. Dehydration of the aldoxime to the nitrile occurs upon treatment with acetic anhydride ...