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Mentha arvensis oil exhibits repellent acute toxic and antioxidant activities in Nauphoeta cinerea. [PDF]
Alonso Leite Dos Santos C +8 more
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Combined Cytotoxic Effects of Carvacrol-Based Essential Oil Formulations. [PDF]
Gönül Geyik Ö +3 more
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Comparative Phytochemical Analysis of the Aerial Parts of <i>Pelargonium radula</i> and <i>Geranium macrorrhizum</i> Cultivated in Bulgaria Using GC-MS and HPLC. [PDF]
Sabotinova D +5 more
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Antioxidant and Antifungal Effects of Six Plant Essential Oils Against <i>Penicillium digitatum</i> and <i>Penicillium italicum</i>. [PDF]
García-Custodio MDC +4 more
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Selected Essential Oils Act as Repellents Against the House Cricket, Acheta domesticus. [PDF]
Heinbockel TK +3 more
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Bulletin of the Academy of Sciences, USSR Division of Chemical Science, 1963
1. It was shown that the optical inversion of the 2,4-dinitrophenylhydrazone of menthone occurs under the action of trichloroacetic acid. 2. It was shown that optically active and racemic alkoxides have different catalytic effects on the optical inversion of menthone.
E. I. Klabunovskii +2 more
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1. It was shown that the optical inversion of the 2,4-dinitrophenylhydrazone of menthone occurs under the action of trichloroacetic acid. 2. It was shown that optically active and racemic alkoxides have different catalytic effects on the optical inversion of menthone.
E. I. Klabunovskii +2 more
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Oxidation of menthone oxothiolane
Chemistry of Natural Compounds, 2008meta-Chloroperoxybenzoic acid (m-ClPBA) was shown to be an oxidant for two stereoisomers of menthone oxothiolane. The effect of steric factors on the ability to oxidize the sulfide group was found. Oxidation of (5S,6S,9R)-6-isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane to the sulfone was prevented by the steric proximity of an isopropyl group to the
A. V. Timshina +6 more
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Chiral perrocenylalkylamines from (-)-menthone
Tetrahedron, 1986Abstract Three enantiomerically pure ∝-ferrocenylalkylamines are directly obtained from (-)-menthone. The isomerizations of the ∝-ferrocenylalkyl carbocation intermediates are studied and exploited in stereoselective syntheses. These carbocations are the basis of the configurational assignment of the amines.
Franz Siglmüller +2 more
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