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- W2087614057 abstract "4-Alkoxy substituted 1,3,2-dioxaborinanes 1, readily available from β-keto esters, undergo substitution reactions under mild reaction conditions with primary and secondary amines, deriving the 4-alkylamino analogue 2. Reactions of 1 with substituted phenylhydrazines gave the corresponding hydrazones, or pyrazolones, and 5-alkoxy-1H-pyrazoles as a mixture of products." @default.
- W2087614057 created "2016-06-24" @default.
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- W2087614057 date "2007-11-01" @default.
- W2087614057 modified "2023-10-09" @default.
- W2087614057 title "Aminolysis of 2,2-difluoro-4-alkoxy-1,3,2-dioxaborinanes: route to β-keto amides and β-enamino carboxamides" @default.
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- W2087614057 doi "https://doi.org/10.1016/j.tet.2007.08.085" @default.
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