Chelation-controlled reduction: Stereoselective formation of syn-1,3-diols and synthesis of compactin and mevinolin lactone

Journal of Organic Chemistry

Volumn 67, Issue 25, 2002, Pages 8783-8788

  Ghosh, Arun K ^a   Lei, Hui ^a  

^a UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

STEREOSELECTIVE FORMULATION;

ALDEHYDES; CHELATION; ENZYME INHIBITION; SYNTHESIS (CHEMICAL);

KETONES;

ALDEHYDE; COMPACTIN; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; KETONE; LACTONE; MEVINOLIN; NITRO DERIVATIVE; ALCOHOL DERIVATIVE; CHELATING AGENT; DRUG DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; LITHIUM;

ALDOL REACTION; ARTICLE; CHELATION; CHEMICAL REACTION; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; REDUCTION; STEREOCHEMISTRY; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; METHODOLOGY; ORGANIC CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALCOHOLS; CATALYSIS; CHELATING AGENTS; CHEMISTRY, ORGANIC; HYDROXYMETHYLGLUTARYL-COA REDUCTASE INHIBITORS; INDICATORS AND REAGENTS; LACTONES; LITHIUM; LOVASTATIN; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 0037073815     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo020402k     Document Type: Article

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