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pubmed-article:18399199rdf:typepubmed:Citationlld:pubmed
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pubmed-article:18399199pubmed:issue3lld:pubmed
pubmed-article:18399199pubmed:dateCreated2008-4-10lld:pubmed
pubmed-article:18399199pubmed:abstractTextA photochromic diarylethene containing naphthyl groups formed a chiral crystal when co-crystallized with octafluoronaphthalene, although both molecules are achiral, and underwent highly enantioselective photocyclization owing to the conformational confinement in the crystal.lld:pubmed
pubmed-article:18399199pubmed:languageenglld:pubmed
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pubmed-article:18399199pubmed:authorpubmed-author:IrieMasahiroMlld:pubmed
pubmed-article:18399199pubmed:authorpubmed-author:KobatakeSeiya...lld:pubmed
pubmed-article:18399199pubmed:authorpubmed-author:MorimotoMasak...lld:pubmed
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pubmed-article:18399199pubmed:pagination335-7lld:pubmed
pubmed-article:18399199pubmed:year2008lld:pubmed
pubmed-article:18399199pubmed:articleTitleAbsolute asymmetric photocyclization in chiral diarylethene co-crystals with octafluoronaphthalene.lld:pubmed
pubmed-article:18399199pubmed:affiliationDepartment of Chemistry, Rikkyo University, Nishi-Ikebukuro 3-34-1, Toshima-ku, Tokyo 171-8501, Japan. m-morimoto@rikkyo.ac.jplld:pubmed
pubmed-article:18399199pubmed:publicationTypeJournal Articlelld:pubmed