Arene Ruthenium(II) Carboxylates for C─H Alkylations and Arylations at Near Room Temperature. [PDF]
Hou X +4 more
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Co-application of arbuscular mycorrhizal fungi and putrescine improves essential oil production and drought tolerance in Cuminum cyminum L. [PDF]
Anjam HR, Hosseinifarahi M, Abdipour M.
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Unlocking the Aromatic Profile of Wild-Grown Croatian Fennel: A Comparative Study of Essential Oils and Hydrolates. [PDF]
Vučak A +5 more
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Volatile Compounds as Upcoming Antigiardial Agents: In Vitro Action of Carvacrol, Thymol and p-Cymene on <i>Giardia lamblia</i> Trophozoites. [PDF]
Machado M +4 more
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Multifunctional Activity of <i>Lippia gracilis</i> Schauer Essential Oil Against Skin Infections. [PDF]
Soares IL +5 more
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Ru(ii)-catalyzed regioselective (3 + 2)-annulation of anilines with allenes to access 2-vinylindoles. [PDF]
Dash OP, Singh A, Shukla RK, Volla CMR.
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Health beneficial and pharmacological properties of p-cymene
Food and Chemical Toxicology, 2021p-cymene also known as p-cymol or p-isopropyltoluene is an alkyl-substituted aromatic compound naturally occurring in essential oils (EOs) of various aromatic plants, including the genus of Artemisia, Protium, Origanum, and Thymus. It is related to the family of terpenes, especially monocyclic monoterpenes.
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Nonclassical oxidation of cymenes
Journal of the Chemical Society D: Chemical Communications, 1971Cobalt(III) ion-catalysed co-oxidation of p-cymene and butane affords predominantly p-isopropylbenzoic acid, contrary to the prediction based on the classical free-radical mechanism.
Anatoli Onopchenko +2 more
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AbstractNitrierung von p‐Cymol (I) in Acetanhydrid liefert ein Gemisch der cisund trans‐Nitroacetate (II) (Hauptprodukt), die Nitrocymole (III) und das Nitrotoluol (IV).
ALFRED FISCHER, ROLF ROEDERER
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