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pubmed-article:15548070pubmed:dateCreated2004-11-19lld:pubmed
pubmed-article:15548070pubmed:abstractTextThe ADE fragment of nakadomarin A has been synthesized in nine linear steps from commercial material. The key transformation is an asymmetric azomethine ylide [1,3]-dipolar cycloaddition to establish the AD-spirocyclic system containing three of the four stereocenters of the natural product. [reaction: see text]lld:pubmed
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pubmed-article:15548070pubmed:authorpubmed-author:WilliamsRober...lld:pubmed
pubmed-article:15548070pubmed:authorpubmed-author:AhrendtKateri...lld:pubmed
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pubmed-article:15548070pubmed:pagination4539-41lld:pubmed
pubmed-article:15548070pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:15548070pubmed:articleTitleA concise asymmetric synthesis of the ADE fragment of nakadomarin A.lld:pubmed
pubmed-article:15548070pubmed:affiliationDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523-1872, USA.lld:pubmed
pubmed-article:15548070pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15548070pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:15548070pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed