Stereoselective synthesis and absolute configuration of the C1′-C25′ fragment of symbiodinolide

Journal of Organic Chemistry

Volumn 74, Issue 17, 2009, Pages 6658-6666

  Takamura, Hiroyoshi ^a   Murata, Takeshi ^b   Asai, Takahiro ^b   Kadota, Isao ^a   Uemura, Daisuke ^c  

^a OKAYAMA UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY   (Japan)

^c KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; ALKALINE HYDROLYSIS; CHEMICAL EQUATIONS; DEGRADED PRODUCTS; OLEFINATION; SIDE CHAINS; STEREOSELECTIVE SYNTHESIS; SYNTHETIC ROUTES;

STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

STEREOSELECTIVITY;

MACROLIDE; SYMBIODINOLIDE; UNCLASSIFIED DRUG;

ALKALINIZATION; ARTICLE; DEGRADATION KINETICS; ENANTIOMER; HYDROLYSIS; JULIA KOCIENSKI OLEFINATION; KOTSUKI COUPLING REACTION; NONHUMAN; OLEFINATION; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

CARBON; CHEMISTRY, ORGANIC; ETHERS; HYDROLYSIS; MACROCYCLIC COMPOUNDS; MODELS, CHEMICAL; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; MOLECULAR WEIGHT; STEREOISOMERISM;

EID: 69549108652     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901162v     Document Type: Article

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