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Volumn 74, Issue 22, 2009, Pages 8826-8829
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Total syntheses of all stereoisomers of phenatic acid B
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Author keywords
[No Author keywords available]
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Indexed keywords
ABSOLUTE CONFIGURATION;
ASYMMETRIC DIHYDROXYLATION;
CHEMICAL EQUATIONS;
HYDROBORATION-OXIDATION;
JOHNSON-CLAISEN REARRANGEMENTS;
SYNTHETIC STRATEGIES;
TOTAL SYNTHESIS;
ACIDS;
ETHERS;
STEREOCHEMISTRY;
SYNTHESIS (CHEMICAL);
ANTIFUNGAL AGENT;
ANTIINFECTIVE AGENT;
NATURAL PRODUCT;
PHENATIC ACID B;
UNCLASSIFIED DRUG;
ACHOLEPLASMA LAIDLAWII;
ANTIBACTERIAL ACTIVITY;
ANTIFUNGAL ACTIVITY;
ARTICLE;
BACILLUS SUBTILIS;
BACTEROIDES FRAGILIS;
CANDIDA ALBICANS;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
DRUG ISOLATION;
NONHUMAN;
PROTON NUCLEAR MAGNETIC RESONANCE;
STAPHYLOCOCCUS AUREUS;
STEREOCHEMISTRY;
STEREOISOMERISM;
STREPTOMYCES;
SYNTHESIS;
ACETIC ACIDS;
CRYSTALLOGRAPHY, X-RAY;
MODELS, MOLECULAR;
MOLECULAR STRUCTURE;
PHENOLS;
STEREOISOMERISM;
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EID: 70449632674
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo901927w Document Type: Article |
Times cited : (28)
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References (23)
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