Synthesis and structural revision of symbiodinolide C23-C34 fragment

Journal of Organic Chemistry

Volumn 74, Issue 13, 2009, Pages 4797-4803

  Murata, Takeshi ^a   Sano, Masayuki ^a   Takamura, Hiroyoshi ^b   Kadota, Isao ^b   Uemura, Daisuke ^c  

^a NAGOYA UNIVERSITY   (Japan)

^b OKAYAMA UNIVERSITY   (Japan)

^c KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; DEGRADED PRODUCTS; DIASTEREOMERS; L-ASPARTIC ACID; SPECTROSCOPIC DATA; STEREOSELECTIVE SYNTHESIS; SYNTHETIC PRODUCTS;

CHEMICAL INDUSTRY; ORGANIC ACIDS; STEREOCHEMISTRY; STEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

ASPARTIC ACID; EPOXIDE; ETHYLENE; POLYOL; SYMBIODINOLIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONJUGATION; DIASTEREOISOMER; SPECTROSCOPY; STANDARD; STEREOCHEMISTRY; SYNTHESIS;

ASPARTIC ACID; CATALYSIS; MACROCYCLIC COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 67649625261     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900546k     Document Type: Article

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27. 3OH).
28. 1H NMR spectra of the synthetic 20 and 22 were clearly different from those of the degraded C23-C34 fragment, respectively.