Study on the Intramolecular Cyclization through Opening of Epoxide Ⅳ. Cyclization of N-Methyl-N-benz

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Intramolecular cyclization of β -methyl substituted epoxide under aprotics (e.g. LDA in benzene) and protic conditions (e.g. LiOH in MeOH/H2O)both gave a mixture of β-, γ-, δ- and ε-lactam but in different ratio.
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