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pubmed-article:19082120pubmed:issue46lld:pubmed
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pubmed-article:19082120pubmed:abstractTextDiastereoisomeric hydroformylation catalysts show differences for the catalyst preformation pathway and a strongly reduced n-octene hydroformylation activity for the (S,S,R)-isomer.lld:pubmed
pubmed-article:19082120pubmed:languageenglld:pubmed
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pubmed-article:19082120pubmed:authorpubmed-author:BaumannWolfga...lld:pubmed
pubmed-article:19082120pubmed:authorpubmed-author:BörnerArminAlld:pubmed
pubmed-article:19082120pubmed:authorpubmed-author:SelentDetlefDlld:pubmed
pubmed-article:19082120pubmed:authorpubmed-author:WieseKlaus-Di...lld:pubmed
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pubmed-article:19082120pubmed:year2008lld:pubmed
pubmed-article:19082120pubmed:articleTitleDiastereoisomeric bisphosphite ligands in the hydroformylation of octenes: rhodium catalysis and HP-NMR investigations.lld:pubmed
pubmed-article:19082120pubmed:affiliationLeibniz-Institut für Katalyse an der Universität Rostock e.V., A.-Einstein-Str., 29a, 18059, Rostock, Germany. detlef.selent@catalysis.delld:pubmed
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