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- W4255365722 abstract "Enantiomerenangereicherte Chlorhydrine sind durch Desymmetrisierung aus meso-Epoxiden zugänglich. Chirale Arylphosphonsäureamide wie 1 katalysieren die Ringöffnung der Epoxide durch SiCl4 zu den entsprechenden Chlorhydrinen in guten Ausbeuten (bis zu 95%) und Enantiomerenüberschüssen (bis zu >99% ee)." @default.
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- W4255365722 date "2000-07-17" @default.
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- W4255365722 title "Beneficial Effect ofortho-Methoxy Groups in the Asymmetric Ring Opening ofmeso Epoxides with Silicon Tetrachloride Catalyzed by Chiralortho-Methoxyphenyldiazaphosphonamide Lewis Bases" @default.
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- W4255365722 doi "https://doi.org/10.1002/1521-3757(20000717)112:14<2654::aid-ange2654>3.0.co;2-q" @default.
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