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pubmed-article:11594811pubmed:abstractText[reaction: see text]. The regioselective and enantiospecific rhodium-catalyzed allylic amination of secondary allylic carbonates 1 with N-(arylsulfonyl)anilines provides a convenient process for the construction of arylamines 2. This method, in conjunction with ring-closing metathesis and radical cyclization reactions, allows the direct construction of biologically relevant pharmacophores as exemplified by the construction of dihydroquinoline and dihydrobenzo[b]indoline derivatives.lld:pubmed
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pubmed-article:11594811pubmed:authorpubmed-author:EvansP APAlld:pubmed
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pubmed-article:11594811pubmed:articleTitleRegioselective and enantiospecific rhodium-catalyzed allylic amination with N-(arylsulfonyl)anilines.lld:pubmed
pubmed-article:11594811pubmed:affiliationDepartment of Chemistry, Indiana University, Bloomington, Indiana 47405, USA. paevans@indiana.edulld:pubmed
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