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Opposite pi-face selectivity for the DMD and m-CPBA epoxidations of chiral 2,2-dimethyloxazolidine derivatives of tiglic amides: Control by steric interactions versus hydrogen bonding

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Peters,  K.
Former Scientific Facilities, Max Planck Institute for Solid State Research, Max Planck Society;

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Peters,  E.-M.
Former Scientific Facilities, Max Planck Institute for Solid State Research, Max Planck Society;

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Adam, W., Pastor, A., Peters, K., & Peters, E.-M. (2000). Opposite pi-face selectivity for the DMD and m-CPBA epoxidations of chiral 2,2-dimethyloxazolidine derivatives of tiglic amides: Control by steric interactions versus hydrogen bonding. Organic Letters, 2, 1019-1022.


Cite as: https://hdl.handle.net/21.11116/0000-000E-EAAB-A
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