Design, Synthesis and Fungicidal Activity of Novel Sclerotiorin Derivatives

Chemical Biology and Drug Design

Volumn 80, Issue 5, 2012, Pages 682-692

  Lin, Long ^a   Mulholland, Nick ^b   Huang, Shao Wei ^a   Beattie, David ^b   Irwin, Dianne ^b   Gu, Yu Cheng ^b   Clough, John ^b   Wu, Qiong You ^a   Yang, Guang Fu ^a  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

^b JEALOTT S HILL INTERNATIONAL RESEARCH CENTRE   (United Kingdom)

Author keywords

Antifungal activity; Azaphilone; Natural product; Sclerotiorin; Structural modification

Indexed keywords

2,4 DIHYDROXY 3,5 DIMETHYL 6 (2 PHENYLETHYNYL)BENZALDEHYDE; 3 BROMO 4,6 DIHYDROXY 5 METHYL 2 (2 PHENYLETHYNYL)BENZALDEHYDE; 6 ETHYNYL 2,4 DIHYDROXY 3 METHYLBENZALDEHYDE; 7 HYDROXY 5,7 DIMETHYL 3 PHENYLISOCHROMAN 6,8 DIONE; ALIPHATIC COMPOUND; ALKADIENE; ANTIFUNGAL AGENT; NATURAL PRODUCT; PHENYL GROUP; SCLEROTIORIN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CONTROLLED STUDY; CYCLOISOMERIZATION; DRUG DESIGN; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; FUNGICIDAL ACTIVITY; ISOMERIZATION; NONHUMAN; OXIDATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SONOGASHIRA REACTION; X RAY CRYSTALLOGRAPHY;

BENZOPYRANS; FUNGI; FUNGICIDES, INDUSTRIAL; MODELS, MOLECULAR; PENICILLIUM; PLANT DISEASES; PLANTS;

PENICILLIUM SCLEROTIORUM;

EID: 84867230593     PISSN: 17470277     EISSN: 17470285     Source Type: Journal    
DOI: 10.1111/cbdd.12005     Document Type: Article

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