Organoboron-based allylation approach to the total synthesis of the medium-ring dilactone (+)-antimycin A1b

Journal of Organic Chemistry

Volumn 79, Issue 16, 2014, Pages 7415-7424

  Janetzko, John ^a   Batey, Robert A ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLATION; STEREOCHEMISTRY; STEREOSELECTIVITY;

ALLYLATION REACTIONS; AMIDE COUPLINGS; DIASTEREOSELECTIVE; LINEAR SEQUENCE; MACROLACTONIZATION; MONTMORILLONITE K10; STEREOSELECTIVE SYNTHESIS; TOTAL SYNTHESIS;

SYNTHESIS (CHEMICAL);

3 FORMAMIDOSALICYLIC ACID; ALDEHYDE DERIVATIVE; ALPHA SILYLOXY ALDEHYDE; AMIDE; ANTIMYCIN A1; ANTIMYCIN A1B; BORON DERIVATIVE; LACTIC ACID ETHYL ESTER; MONTMORILLONITE; POTASSIUM ALLYLTRIFLUOROBORATE SALT; SALICYLIC ACID DERIVATIVE; SODIUM CHLORIDE; UNCLASSIFIED DRUG; LACTONE; N-FORMAMIDOSALICYLIC ACID;

ALLYLATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROBORATION; MACROLACTONIZATION; STEREOCHEMISTRY; SUBSTITUTION REACTION; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ANTIMYCIN A; BORON COMPOUNDS; LACTONES; MOLECULAR STRUCTURE; SALICYLATES; STEREOISOMERISM;

EID: 84906092072     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo501134d     Document Type: Article

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