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pubmed-article:16719439pubmed:dateCreated2006-5-24lld:pubmed
pubmed-article:16719439pubmed:abstractTextSelf-assembled chiral polymetallic complexes often demonstrate novel properties as asymmetric catalysts. We report the three-dimensional structures of two such asymmetric catalysts (crystals A and B) for Strecker alpha,alpha-disubstituted amino acid synthesis. These complexes are constructed via assembly of the same chiral modules derived from d-glucose, but their assembly modes differ. The enantioselectivity in the Strecker reaction was dramatically switched, depending on which assembly mode was used: the catalyst generated in situ whose structure is represented by crystal B, or by crystal A. These findings provide insight into the functional importance of higher-order structures of an artificial catalyst.lld:pubmed
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pubmed-article:16719439pubmed:authorpubmed-author:YamaguchiKent...lld:pubmed
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pubmed-article:16719439pubmed:authorpubmed-author:DanjoHiroshiHlld:pubmed
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pubmed-article:16719439pubmed:day31lld:pubmed
pubmed-article:16719439pubmed:volume128lld:pubmed
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pubmed-article:16719439pubmed:pagination6768-9lld:pubmed
pubmed-article:16719439pubmed:dateRevised2008-1-17lld:pubmed
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pubmed-article:16719439pubmed:year2006lld:pubmed
pubmed-article:16719439pubmed:articleTitleAssembly state of catalytic modules as chiral switches in asymmetric Strecker amino acid synthesis.lld:pubmed
pubmed-article:16719439pubmed:affiliationGraduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo Bunkyo-ku, Tokyo 113-0033, Japan.lld:pubmed
pubmed-article:16719439pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16719439pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed