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Volumn 67, Issue 12, 2002, Pages 4337-4345
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Stereoselective total syntheses of the racemic form and the natural enantiomer of the marine alkaloid lepadiformine via a novel N-acyliminium ion/allylsilane spirocyclization strategy
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Author keywords
[No Author keywords available]
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Indexed keywords
STEREOSELECTIVITY;
ALKALI METALS;
BROMINE;
SYNTHESIS (CHEMICAL);
ORGANIC CHEMICALS;
ALKALOID;
BENZAMIDE DERIVATIVE;
BROMIDE;
PYROGLUTAMIC ACID;
SILANE;
ARTICLE;
CATALYSIS;
CYCLIZATION;
ENANTIOMER;
HYDROLYSIS;
OXIDATION;
STEREOCHEMISTRY;
SYNTHESIS;
ALKALOIDS;
ANIMALS;
BIOLOGICAL FACTORS;
CATALYSIS;
CHEMISTRY, ORGANIC;
CRYSTALLOGRAPHY, X-RAY;
CYCLIZATION;
INDICATORS AND REAGENTS;
MOLECULAR STRUCTURE;
NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR;
PYRROLIDONECARBOXYLIC ACID;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
UROCHORDATA;
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EID: 0037077015
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo0201070 Document Type: Article |
Times cited : (102)
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References (50)
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