A general strategy for the stereocontrolled preparation of diverse 8- and 9-membered Laurencia -type bromoethers

Journal of the American Chemical Society

Volumn 133, Issue 40, 2011, Pages 15898-15901

  Snyder, Scott A ^a   Treitler, Daniel S ^a   Brucks, Alexandria P ^a   Sattler, Wesley ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETOGENINS; BIOSYNTHESIS PATHWAYS; TETRAHYDROFURANS; TO EFFECT;

BIOCHEMISTRY;

ACETOGENIN; BROMODIETHYLSULFONIUM BROMOPENTACHLOROANTIMONATE; TETRAHYDROFURAN; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; BROMOETHERIFICATION; CHEMICAL REACTION; CYCLIZATION; HYDROLYSIS; LAURENCIA; STEREOCHEMISTRY; X RAY DIFFRACTION;

ACETOGENINS; ETHERS; FURANS; HYDROCARBONS, BROMINATED; LAURENCIA;

EID: 80053540653     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja2069449     Document Type: Article

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