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pubmed-article:14535721pubmed:abstractText[reaction: see text] New monodentate phosphite ligands have been developed from axially chiral biphenols, which show excellent enantioselectivity in the Rh(I)-catalyzed hydrogenation of dimethyl itaconate. The new chiral ligand system is suitable to create libraries and possesses fine-tuning capability.lld:pubmed
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pubmed-article:14535721pubmed:articleTitleSynthesis of new chiral monodentate phosphite ligands and their use in catalytic asymmetric hydrogenation.lld:pubmed
pubmed-article:14535721pubmed:affiliationDepartment of Chemistry, State University of New York at Stony Brook, Stony Brook, New York 11794-3400, USA.lld:pubmed
pubmed-article:14535721pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:14535721pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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