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Asymmetric Route to Pyridines Bearing a Highly Functionalized 2-Alkyl Substituent by Aziridine Ring-Opening Reactions
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文摘
The aziridine prepared from the 2-pyridineimine derived from (S)-valinol underwent ring-opening byattack of nitrogen, sulfur, and oxygen nucleophiles. Complete or prevalent regioselectivity was obtainedusing cerium trichloride heptahydrate as a catalyst. In some cases, the N-substituent could be removedby an oxidative protocol.

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