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pubmed-article:17705538pubmed:abstractTextIr-catalyzed allylic aminations of (E)-4-benzyloxy-2-butenyl methyl carbonate with benzylamine using Feringa's (Sa,Sc,Sc)-phosphoramidite as a chiral ligand afforded linear-aminated achiral product N,O-dibenzyl-4-amino-2-buten-1-ol regioselectively (linear/branched = >99/1), whereas the (E)-5-benzyloxy-2-pentenyl methyl carbonate showed completely opposite regioselectivity (linear/branched = >1/99) and afforded the optically active (3R)-N,O-dibenzylated 3-amino-1-penten-5-ol with very high enantioselectivity (96% ee), which was used as a key intermediate for the effective synthesis of various cyclic beta-amino alcohol derivatives through ring-closing metathesis in high yields.lld:pubmed
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pubmed-article:17705538pubmed:authorpubmed-author:LeeSang-giSGlld:pubmed
pubmed-article:17705538pubmed:authorpubmed-author:LeeJun HeeJHlld:pubmed
pubmed-article:17705538pubmed:authorpubmed-author:ShinSeunghoon...lld:pubmed
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pubmed-article:17705538pubmed:year2007lld:pubmed
pubmed-article:17705538pubmed:articleTitleIr-catalyzed allylic amination/ring-closing metathesis: a new route to enantioselective synthesis of cyclic beta-amino alcohol derivatives.lld:pubmed
pubmed-article:17705538pubmed:affiliationDivision of Nano Science (BK21)/Department of Chemistry, Ewha Womans University, 11-1 Daehyun-Dong, Seodaemun-Gu, 120-750 Seoul, Korea.lld:pubmed
pubmed-article:17705538pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17705538pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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