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

Article

Fecha

2016

Registro en:

17, 6, -

16616596

https://hdl.handle.net/20.500.12728/6279

https://repositorioslatinoamericanos.uchile.cl/handle/2250/5145940

Autor

Soto M.

Espinoza L.

Chávez M.I.

Díaz K.

Olea A.F.

Taborga L.

Institución

Universidad Autónoma de Chile

Materias

Botrytis cinerea

Geranylated phenol derivatives

Growth inhibition effect

Hydrated geranyl

Structural elucidation

2 ((2 hydroxy 2,6,6 trimethylcyclohexyl)methyl) 5 methoxybenzene 1,4 diol

2 (3,7 dihydroxy 3, 7 dimethyloctyl) 5 methoxybenzene 1,4 diol

2 (3,7 dimethylocta 2,6 dien 1 yl) 5 methoxycyclohexa 2,5 diene 1,4 dione

2 (3,7 dimethylocta 2,6 dienyl) 4 methylphenol

2 (3,7 dimethylocta 2,6 dienyl) 4 methylphenyl acetate

2 (3,7 dimethylocta 2,6 dienyl) 5 methoxy 1,4 phenylene diacetate

2 (3,7 dimethylocta 2,6 dienyl) 5 methoxybenzene 1,4 diol

2 geranylhydroquinone

2 geranylquinone

2,5 bisgeranylquinone

3,5 bis( 3,7-dimethylocta 2,6 dienyl) 2 methoxycyclohexa 2,5 diene 1,4 dione

4 (3,7 dimethylocta 2,6 dienyl) 2 methylphenol

8 (2 hydroxy 3 methylphenyl) 2,6 dimethyloctane 2,6 diol

8 (4 hydroxy 3 methylphenyl) 2,6 dimethyloctane 2,6 diol

geranylated phenol derivative

phenol derivative

quinone derivative

unclassified drug

antifungal agent

phenol derivative

antifungal activity

Botrytis cinerea

carbon nuclear magnetic resonance

chemical structure

column chromatography

controlled study

infrared spectroscopy

nuclear Overhauser effect

proton nuclear magnetic resonance

thin layer chromatography

microbial sensitivity test

Antifungal Agents

Microbial Sensitivity Tests

Molecular Structure

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