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pubmed-article:10836050pubmed:abstractText[formula: see text] Regioselective rhodium-catalyzed allylic amination followed by ring-closing metathesis, using the Grubbs' catalyst, provides an expeditious route to monosubstituted azacycles. The enantiomerically enriched allylamine 1 can also be resubjected to the reaction sequence with (R)- and (S)-2b to facilitate the diastereospecific construction of 2,5-disubstituted pyrrolines 3/4.lld:pubmed
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pubmed-article:10836050pubmed:authorpubmed-author:RobinsonJ EJElld:pubmed
pubmed-article:10836050pubmed:authorpubmed-author:EvansP APAlld:pubmed
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pubmed-article:10836050pubmed:articleTitleRegioselective Rh-catalyzed allylic amination/ring-closing metathesis approach to monocyclic azacycles: diastereospecific construction of 2,5-disubstituted pyrrolines.lld:pubmed
pubmed-article:10836050pubmed:affiliationBrown Laboratory, Department of Chemistry and Biochemistry, University of Delaware, Newark 19716, USA. paevans@udel.edulld:pubmed
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