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- W2135333643 abstract "Eine überraschend selektive, nichtenzymatische kinetische Racematspaltung von leicht erhältlichen, racemischen β-chiralen Ketonen ermöglichte den Titelprozess, mit dem die rasche Synthese einiger bioaktiver Flavanone in nahezu enantiomerenreiner Form gelang (siehe Schema; MOM=Methoxymethyl, Ts= p-Toluolsulfonyl). As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2135333643 date "2013-09-11" @default.
- W2135333643 modified "2023-10-18" @default.
- W2135333643 title "Ein praktischer Zugang zu hoch enantiomerenreinen Flavanonen durch katalytische asymmetrische Transferhydrierung" @default.
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- W2135333643 doi "https://doi.org/10.1002/ange.201306500" @default.
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