Stereoretentive suzuki-miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-Peridinin

Journal of the American Chemical Society

Volumn 132, Issue 20, 2010, Pages 6941-6943

  Woerly, Eric M ^a   Cherney, Alan H ^a   Davis, Erin K ^a   Burke, Martin D ^a  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID; BUILDING BLOCKES; CROSS-COUPLINGS; FUNCTIONALIZED; NATURAL PRODUCTS; PERIDININ; SMALL MOLECULES; STRUCTURE/FUNCTION RELATIONSHIPS; SUZUKI-MIYAURA COUPLING; TOTAL SYNTHESIS;

BORON; BORON COMPOUNDS; BORON DEPOSITS;

SYNTHESIS (CHEMICAL);

ALKYNE; ALLENE DERIVATIVE; BORONIC ACID DERIVATIVE; CAROTENOID; PERIDININ; PHOSPHINE; UNCLASSIFIED DRUG;

ARTICLE; CROSS COUPLING REACTION; HYDROBORATION; STEREOCHEMISTRY; SUZUKI REACTION; SYNTHESIS;

ALKADIENES; CAROTENOIDS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 77952561793     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja102721p     Document Type: Article

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