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pubmed-article:12841233pubmed:issue12lld:pubmed
pubmed-article:12841233pubmed:dateCreated2003-7-4lld:pubmed
pubmed-article:12841233pubmed:abstractTextLithiation and alkylation of a 2-isopropylidineaziridine bearing an (S)-alpha-methylbenzyl group on nitrogen proceeds with high levels of diastereocontrol (80-90% de).lld:pubmed
pubmed-article:12841233pubmed:languageenglld:pubmed
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pubmed-article:12841233pubmed:authorpubmed-author:RoweG DGDlld:pubmed
pubmed-article:12841233pubmed:authorpubmed-author:HayesJ FJFlld:pubmed
pubmed-article:12841233pubmed:authorpubmed-author:ShipmanMMlld:pubmed
pubmed-article:12841233pubmed:authorpubmed-author:PrévostNNlld:pubmed
pubmed-article:12841233pubmed:authorpubmed-author:ProkesIIlld:pubmed
pubmed-article:12841233pubmed:authorpubmed-author:SlawinA M ZAMlld:pubmed
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pubmed-article:12841233pubmed:year2003lld:pubmed
pubmed-article:12841233pubmed:articleTitleAziridinyl anions from a chiral, nonracemic 2-isopropylidineaziridine: surprisingly diastereoselective alkylation reactions.lld:pubmed
pubmed-article:12841233pubmed:affiliationGlaxoSmithKline, Old Powder Mills, Tonbridge, Kent, UK TN11 9AN.lld:pubmed
pubmed-article:12841233pubmed:publicationTypeJournal Articlelld:pubmed