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pubmed-article:12889907pubmed:dateCreated2003-7-31lld:pubmed
pubmed-article:12889907pubmed:abstractText[reaction: see text] Intramolecular cyclizations of a series of (E)- and (Z)-olefinic acyclic ketone-derived N-acyliminium ions have been studied. It has been found that both the course of the reaction and the stereochemistry of the products are critically dependent upon the tether length and olefin geometry of the cyclization substrate.lld:pubmed
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pubmed-article:12889907pubmed:authorpubmed-author:WeinrebSteven...lld:pubmed
pubmed-article:12889907pubmed:authorpubmed-author:ChaoWenchunWlld:pubmed
pubmed-article:12889907pubmed:authorpubmed-author:WaldmanJacob...lld:pubmed
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pubmed-article:12889907pubmed:pagination2915-8lld:pubmed
pubmed-article:12889907pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:12889907pubmed:year2003lld:pubmed
pubmed-article:12889907pubmed:articleTitleStudies of intramolecular cyclizations of N-acyliminium ions derived from acyclic ketones: unanticipated stereochemical and structural results.lld:pubmed
pubmed-article:12889907pubmed:affiliationDepartment of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.lld:pubmed
pubmed-article:12889907pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12889907pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:12889907pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed