An intramolecular Diels-Alder approach to the eunicellins: Enantioselective total syntheses of ophirin B and astrogorgin

被引：0

作者：

Crimmins, Michael T. ^{[1
]}

Brown, Brandon H. ^{[2
]}

Plake, Hilary R. ^{[1
]}

机构：

[1] Department of Chemistry, Venable and Kenan Laboratories of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3290, United States

[2] Gilead Sciences, Inc., Foster City, CA 94404, United States

来源：

Journal of the American Chemical Society | 1600年 / 128卷 / 04期

关键词：

The enantioselective syntheses of the eunicellins ophirin B and astrogorgin have been completed. Ring-closing metatheses provide efficient access to the oxonene rings; and highly diastereoselective intramolecular Diels-Alder reactions resulted in the formation of the hydrobenzofuran portion of the molecules. © 2006 American Chemical Society;

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摘要：

Journal article (JA)

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页码：1371 / 1378