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pubmed-article:12659574pubmed:abstractText[reaction: see text] anti-Aldol reaction of Ti-enolate derived from cis-2-arylsulfonamido-1-acenaphthenyl propionate with representative aldehydes proceeded in excellent yield with high diastereoselectivity. Both enantiomers of cis-2-amino-1-acenaphthenol were synthesized employing lipase-catalyzed kinetic resolution as the key step.lld:pubmed
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pubmed-article:12659574pubmed:authorpubmed-author:GhoshArun KAKlld:pubmed
pubmed-article:12659574pubmed:authorpubmed-author:KimJae-HunJHlld:pubmed
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pubmed-article:12659574pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12659574pubmed:articleTitleHighly diastereoselective anti-aldol reactions utilizing the titanium enolate of cis-2-arylsulfonamido-1- acenaphthenyl propionate.lld:pubmed
pubmed-article:12659574pubmed:affiliationDepartment of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607, USA. arunghos@uic.edulld:pubmed
pubmed-article:12659574pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12659574pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed