Syntheses of (+)-30-epi-, (-)-6-epi-, (±)-6,30-epi-13,14-Didehydroxyisogarcinol and (±)-6,30-epi-Garcimultiflorone A Utilizing Highly Diastereoselective, Lewis Acid-Controlled Cyclizations

Journal of the American Chemical Society

Volumn 138, Issue 44, 2016, Pages 14789-14797

  Boyce, Jonathan H ^a   Eschenbrenner Lux, Vincent ^a   Porco, John A ^a  

^a Boston University   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

STEREOCHEMISTRY; STEREOSELECTIVITY;

ASYMMETRIC SYNTHESIS; CYCLIZATIONS; DIASTEREOMERS; DIASTEREOSELECTIVE; GRAM-SCALE SYNTHESIS; LEWIS ACID; PHLOROGLUCINOL;

ISOMERS;

30 EPI 13,14 DIDEHYDROXYISOGARCINOL; 6 EPI 13,14 DIDEHYDROXYISOGARCINOL; 6,30 EPI 13,14 DIDEHYDROXYISOGARCINOL; 6,30 EPI GARCIMULTIFLORONE A; BRONSTED ACID; LEWIS ACID; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CYCLIZATION; DIASTEREOISOMER; DRUG SYNTHESIS; PROTON TRANSPORT; STEREOISOMERISM; STEREOSELECTIVITY; CHEMICAL STRUCTURE; CHEMISTRY;

CYCLIZATION; LEWIS ACIDS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84994537679     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b09727     Document Type: Article

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