Olefin metathesis-iodoetherification-dehydroiodination strategy for spiroketal subunits of polyether antibiotics

Journal of Organic Chemistry

Volumn 74, Issue 20, 2009, Pages 7774-7780

  Tony, Kurissery A ^a   Dabideen, Darrin ^a   Li, Jialiang ^a   Díaz Hernández, Maria Dolores ^b   Jiménez Barbero, Jesús ^b   Mootoo, David R ^a  

^a CITY UNIVERSITY OF NEW YORK   (United States)

^b CENTRO DE INVESTIGACIONES BIOLÓGICAS   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERIC EFFECT; CHEMICAL EQUATIONS; CONVERGENT SYNTHESIS; DEHYDROIODINATION; MONENSIN A; OLEFIN METATHESIS; SIX-MEMBERED RINGS;

FUNCTIONAL GROUPS; OLEFINS; ORGANIC POLYMERS;

SYNTHESIS (CHEMICAL);

ACETAL; ALCOHOL; ALKENE; ALKENE DERIVATIVE; DIHYDROXYALKENE; MONENSIN A; MONENSIN DERIVATIVE; PENTACYCLIC TRITERPENE; POLYETHER ANTIBIOTIC AGENT; UNCLASSIFIED DRUG;

ARTICLE; BIOTRANSFORMATION; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; CYCLIZATION; DEHYDROIODINATION; DRUG SYNTHESIS; ETHERIFICATION; IODINATION; IODOETHERIFICATION; RING CLOSING METATHESIS; SUBSTITUTION REACTION; SYNTHESIS;

ANTI-BACTERIAL AGENTS; ETHERS; FURANS; HALOGENATION; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; MONENSIN; SPIRO COMPOUNDS;

EID: 70349866024     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9014722     Document Type: Article

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