Synthetic study on top-half (C14-C25) fragment of amphidinolide B, a 26-membered macrolide

Synlett

Volumn , Issue 5, 1999, Pages 573-575

  Ohi, Katsuhide ^a   Nishiyama, Shigeru ^a  

^a KEIO UNIVERSITY   (Japan)

Author keywords

Amphidinolide B; Asymmetric dihydroxylation; Cytotoxic activity; Marine natural products; Umpolung

Indexed keywords

AMPHIDINOLIDE B; CARBON; IODIDE; MACROLIDE; NATURAL PRODUCT;

ARTICLE; DINOFLAGELLATE; DRUG CYTOTOXICITY; DRUG ISOLATION; DRUG SYNTHESIS; HYDROXYLATION; REACTION ANALYSIS;

EID: 0032908183     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2697     Document Type: Article

References (18)

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18. 3) δ 211.4, 136.0, 129.6, 129.5, 127.6, 127.4, 87.6, 78.0, 75.4, 71.8, 67.7, 67.2, 66.2, 47.5, 45.1, 43.3, 33.0, 29.8, 27.0, 24.3, 19.3, and 16.1. Similar selectivities of related asymmetric dihydroxylation were reported (references 4a, d).