Total synthesis and configurational assignment of the marine natural product haliclamide

Journal of Organic Chemistry

Volumn 78, Issue 6, 2013, Pages 2553-2563

  Pfeiffer, Bernhard ^a   Speck Gisler, Sandra ^a   Barandun, Luzi ^a   Senft, Ursula ^a   De Groot, Claire ^a   Lehmann, Irène ^b   Ganci, Walter ^b   Gertsch, Jürg ^a   Altmann, Karl Heinz ^a  

^a ETH ZURICH   (Switzerland)

^b UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; ANTI-PROLIFERATIVE ACTIVITIES; ANTIBIOTIC ACTIVITY; HUMAN CANCER CELLS; MACRO-CYCLIZATION; MARINE NATURAL PRODUCTS; METATHESIS REACTIONS; RING-CLOSING OLEFIN METATHESIS;

CELL CULTURE; ISOMERS; OLEFINS; STEREOCHEMISTRY;

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ALKADIENE; ALKENE; ANTINEOPLASTIC AGENT; CARBON; HALICLAMIDE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ALLYLATION; ANTINEOPLASTIC ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; DERIVATIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ESTERIFICATION; HUMAN; HUMAN CELL; HYDROGENATION; IC 50; IN VITRO STUDY; MITSUNOBU REACTION; OLEFINATION; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; SAPONIFICATION; STEREOISOMERISM; WITTIG REACTION;

ALKENES; ANTINEOPLASTIC AGENTS; BIOLOGICAL AGENTS; CELL LINE, TUMOR; DEPSIPEPTIDES; HUMANS; MACROLIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84875177536     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3027643     Document Type: Article

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