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Volumn 67, Issue 12, 2002, Pages 4115-4121

Regio- and stereoselective ring openings of 3-aza-2-oxabicyclo[2.2.1]hept-5-ene systems with copper catalyst-modified grignard reagents: Application to the synthesis of an inhibitor of 5-lipoxygenase

(3) Surman, Matthew D a Mulvihill, Mark J a Miller, Marvin J a

a UNIVERSITY OF NOTRE DAME (United States)

Author keywords

[No Author keywords available]

Indexed keywords

RING OPENING;

CATALYSTS; COPPER; MAGNESIUM COMPOUNDS;

AROMATIC HYDROCARBONS;

ARACHIDONATE 5 LIPOXYGENASE; HYDROXAMIC ACID; MAGNESIUM DERIVATIVE; PALLADIUM; REAGENT;

ARTICLE; CATALYSIS; CYCLOADDITION; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

ARACHIDONATE 5-LIPOXYGENASE; AZA COMPOUNDS; BICYCLO COMPOUNDS; CALCIMYCIN; CATALYSIS; CHEMISTRY, ORGANIC; CHROMATOGRAPHY, THIN LAYER; CYCLIZATION; HEPTANES; HUMANS; HYDROXAMIC ACIDS; LIPOXYGENASE INHIBITORS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; STEREOISOMERISM;

EID: 0037076930 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo016275u Document Type: Article

Times cited : (60)

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