Abstract
Oximes such as cyclohexanone oxime and benzaldehyde oxime were catalytically transformed into the corresponding lactams in N,N-dimethylformamide solutions of alkylating reagents such as trialkyloxonium salts. Catalyst turnover attained 43 on the basis of the acid used to obtain alkylating reagent. O-Alkyl-N,N-dimethylformamidinium salt was suggested to be a catalyst species.
Cite
CITATION STYLE
APA
Izumi, Y. (1990). Catalytic Beckmann Rearrangement of Oximes in Homogeneous Liquid Phase. Chemistry Letters, 19(12), 2171–2174. https://doi.org/10.1246/cl.1990.2171
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