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pubmed-article:12027704pubmed:abstractTextSamarium(II) iodide, in the presence of catalytic amounts of nickel(II) iodide, has been used to promote intramolecular conjugate additions of alkyl halides onto alpha,beta-unsaturated lactones. This process has been shown to be applicable to a number of alpha,beta-unsaturated lactones, including tetrasubstituted olefins, and has been demonstrated to be quite general for the formation of saturated bicyclic and tricyclic lactones. The method presented herein provides a mild, efficient process to form structurally complex lactones from simple precursors.lld:pubmed
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pubmed-article:12027704pubmed:authorpubmed-author:MolanderGary...lld:pubmed
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pubmed-article:12027704pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:12027704pubmed:articleTitleSamarium(II) iodide-mediated intramolecular conjugate additions of alpha,beta-unsaturated lactones.lld:pubmed
pubmed-article:12027704pubmed:affiliationRoy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104-6323, USA. gmolandr@sas.upenn.edulld:pubmed
pubmed-article:12027704pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12027704pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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