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- W3134220949 endingPage "152971" @default.
- W3134220949 startingPage "152971" @default.
- W3134220949 abstract "A simultaneous unsymmetrical N,N'-functionalization of hydrazine was realized by a base-mediated insertion into Morita–Baylis–Hillman (MBH) ketones. The atom-economic transformation involves the formation of two carbon–nitrogen bonds accompanied by the cleavage of a carbon–carbon bond, and results in the formation of N-acyl-N'-alkyl substituted hydrazines in good yields over a range of MBH ketones. The products were further transformed to new 2-imino-3-alkyl-1,3,4-oxadiazole analogs." @default.
- W3134220949 created "2021-03-15" @default.
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- W3134220949 date "2021-04-01" @default.
- W3134220949 modified "2023-09-23" @default.
- W3134220949 title "Unsymmetrical N,N'-functionalization of hydrazine by insertion into Morita–Baylis–Hillman ketones" @default.
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- W3134220949 doi "https://doi.org/10.1016/j.tetlet.2021.152971" @default.
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