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File:IsovelleralPreparationViaSwernOxidation.png

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English: Preparation of isovelleral via Swern oxidation. Note that the acid-sensitive cyclopropanemethanol moiety does not undergo ring opening. Taken from (a) Thompson SK, Heathcock CH. "Total synthesis of some marasmane and lactarane sesquiterpenes", Journal of Organic Chemistry, 1992, 57 (22), 5979–5989. doi:10.1021/jo00048a036 (b) Bell RPL, Wijnberg JPBA, de Groot A. "A Novel Route to the Marasmane Skeleton via a Tandem Rearrangement-Cyclopropanation Reaction. Total Synthesis of (+)-Isovelleral", Journal of Organic Chemistry 2001, 66, 2350-2357. doi:10.1021/jo0015568
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current05:22, 3 January 2010Thumbnail for version as of 05:22, 3 January 20101,518 × 356 (23 KB)Walkerma (talk | contribs){{Information |Description={{en|1=Preparation of isovelleral via Swern oxidation. Note that the acid-sensitive cyclopropanemethanol moiety does not undergo ring opening. Taken from (a) Thompson SK, Heathcock CH. "Total synthesis of some marasmane and l

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