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  2. Phenylpropene - Wikipedia

    en.wikipedia.org/wiki/Phenylpropene

    trans-Propenylbenzene (trans-1-phenylpropene) α-Methylstyrene (2-phenylpropene) Allylbenzene (3-phenylpropene) This page was last edited on 21 October ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  4. Schenck ene reaction - Wikipedia

    en.wikipedia.org/wiki/Schenck_ene_reaction

    Many hydroperoxides derived from fatty acids, steroids, and terpenes are also formed via the Schenck ene reaction. For instance, the generation of cis-3-hexenal from linolenic acid: Cis-3-hexenal is generated by conversion of linolenic acid to the hydroperoxide by the action of a lipoxygenase followed by the lyase-induced formation of the ...

  5. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    prop-1-ene-1,2,3-tricarboxylic acid: ... CH 3 (CH 2) 7 COOH benzene-1,3,5-tricarboxylic acid: ... 3 (COOH) 3 (E)-3-phenylprop-2-enoic acid: cinnamic acid trans ...

  6. Cinnamyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl_alcohol

    Cinnamyl alcohol or styron [2] is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure.

  7. Enediyne - Wikipedia

    en.wikipedia.org/wiki/Enediyne

    In 2024, Shen and coworkers disclosed further studies on the biosynthesis of enediynes and reported evidence for a diiodinated trienetetrayne ((13Z)-2,13-diiodopentadeca-1,7,13-triene-3,5,9,11-tetrayne) derived from pentadeca-1,3,5,7,9,11,13-heptaene as a common biosynthetic intermediate for the three known families of enediyne natural products.

  8. Phenylpropiolic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropiolic_acid

    Phenylpropiolic acid, C 6 H 5 CCCO 2 H, formed by the action of alcoholic potash on cinnamic acid dibromide, C 6 H 5 CHBrCHBrCO 2 H, crystallizes in long needles or prisms which melt at 136–137 °C. When heated with water to 120 °C, it yields phenylacetylene (C 6 H 5 CCH).

  9. Taxagifine - Wikipedia

    en.wikipedia.org/wiki/Taxagifine

    11-Hydroxy-13-oxo-12,17-epoxy-12α-tax-4(20)-ene-2α,5α,7β,9α,10β-pentayl 2,7,9,10-tetraacetate 5-[(2E)-3-phenylprop-2-enoate] Systematic IUPAC name (1 S ,3a R ,4 R ,5 R ,5a R ,7 S ,9 S ,9a S ,10 R ,11 S ,11a R )-11a-Hydroxy-1,3a,9a-trimethyl-6-methylidene-13-oxotetradecahydro-1,4-ethanobenzo[5,6]cycloocta[1,2- c ]furan-5,7,9,10,11-pentayl ...