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Volumn 67, Issue 9, 2002, Pages 2954-2959
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Total synthesis of (S)-(+)-imperanene. Effective use of regio- and enantioselective intramolecular carbon-hydrogen insertion reactions catalyzed by chiral dirhodium(II) carboxamidates
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Author keywords
[No Author keywords available]
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Indexed keywords
ELIMINATION PROCESS;
ALKYLATION;
CATALYSIS;
CATALYSTS;
FRIEDEL-CRAFTS REACTION;
SYNTHESIS (CHEMICAL);
ANTIINFLAMMATORY AGENT;
CINNAMIC ACID;
DIRHODIUM CARBOXAMIDATE;
DIURETIC AGENT;
IMPERANENE;
RHODIUM DERIVATIVE;
UNCLASSIFIED DRUG;
ALKYLATION;
ARTICLE;
CATALYSIS;
CHEMICAL REACTION;
CHINESE MEDICINE;
CHIRALITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOSELECTIVITY;
OPTICAL ROTATION;
STEREOCHEMISTRY;
ALKYLATION;
CATALYSIS;
CINNAMATES;
MAGNETIC RESONANCE SPECTROSCOPY;
MEDICINE, CHINESE TRADITIONAL;
MOLECULAR STRUCTURE;
ORGANOMETALLIC COMPOUNDS;
PHENOLS;
PLANTS, MEDICINAL;
RHODIUM;
STEREOISOMERISM;
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EID: 0037012833
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo016220s Document Type: Article |
Times cited : (60)
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References (33)
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