Synthesis of new hydrated geranylphenols and in vitro antifungal activity against botrytis cinerea

dc.creatorSoto M.
dc.creatorEspinoza L.
dc.creatorChávez M.I.
dc.creatorDíaz K.
dc.creatorOlea A.F.
dc.creatorTaborga L.
dc.date.accessioned2020-09-02T22:28:38Z
dc.date.accessioned2022-11-08T20:26:07Z
dc.date.available2020-09-02T22:28:38Z
dc.date.available2022-11-08T20:26:07Z
dc.date.created2020-09-02T22:28:38Z
dc.date.issued2016
dc.identifier17, 6, -
dc.identifier16616596
dc.identifierhttps://hdl.handle.net/20.500.12728/6279
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5145940
dc.languageen
dc.publisherMDPI AG
dc.subjectBotrytis cinerea
dc.subjectFungicide
dc.subjectGeranylated phenol derivatives
dc.subjectGrowth inhibition effect
dc.subjectHydrated geranyl
dc.subjectStructural elucidation
dc.subjectSynthesis
dc.subject2 ((2 hydroxy 2,6,6 trimethylcyclohexyl)methyl) 5 methoxybenzene 1,4 diol
dc.subject2 (3,7 dihydroxy 3, 7 dimethyloctyl) 5 methoxybenzene 1,4 diol
dc.subject2 (3,7 dimethylocta 2,6 dien 1 yl) 5 methoxycyclohexa 2,5 diene 1,4 dione
dc.subject2 (3,7 dimethylocta 2,6 dienyl) 4 methylphenol
dc.subject2 (3,7 dimethylocta 2,6 dienyl) 4 methylphenyl acetate
dc.subject2 (3,7 dimethylocta 2,6 dienyl) 5 methoxy 1,4 phenylene diacetate
dc.subject2 (3,7 dimethylocta 2,6 dienyl) 5 methoxybenzene 1,4 diol
dc.subject2 geranylhydroquinone
dc.subject2 geranylquinone
dc.subject2,5 bisgeranylquinone
dc.subject3,5 bis( 3,7-dimethylocta 2,6 dienyl) 2 methoxycyclohexa 2,5 diene 1,4 dione
dc.subject4 (3,7 dimethylocta 2,6 dienyl) 2 methylphenol
dc.subject8 (2 hydroxy 3 methylphenyl) 2,6 dimethyloctane 2,6 diol
dc.subject8 (4 hydroxy 3 methylphenyl) 2,6 dimethyloctane 2,6 diol
dc.subjectgeranylated phenol derivative
dc.subjectphenol derivative
dc.subjectquinone derivative
dc.subjectunclassified drug
dc.subjectantifungal agent
dc.subjectphenol derivative
dc.subjectplant extract
dc.subjectantifungal activity
dc.subjectArticle
dc.subjectBotrytis cinerea
dc.subjectcarbon nuclear magnetic resonance
dc.subjectchemical structure
dc.subjectcolumn chromatography
dc.subjectcontrolled study
dc.subjectdrug synthesis
dc.subjectinfrared spectroscopy
dc.subjectnonhuman
dc.subjectnuclear Overhauser effect
dc.subjectproton nuclear magnetic resonance
dc.subjectthin layer chromatography
dc.subjectBotrytis
dc.subjectchemistry
dc.subjectdrug effects
dc.subjectmicrobial sensitivity test
dc.subjectsynthesis
dc.subjectAntifungal Agents
dc.subjectBotrytis
dc.subjectMicrobial Sensitivity Tests
dc.subjectMolecular Structure
dc.subjectPhenols
dc.subjectPlant Extracts
dc.titleSynthesis of new hydrated geranylphenols and in vitro antifungal activity against botrytis cinerea
dc.typeArticle


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