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• W2425444724 abstract "Abstract An unprecedented Bronsted base ionic liquid tuned selective aminolysis of ester carbonyl of acetoacetates is demonstrated to achieve acetoacetamide derivatives. Other imidazolium ionic liquid performs an efficient cyclization catalysis involving acetoacetate-carbonyl groups and o-phenylenediamine at elevated temperature to produce benzimidazoles via C–C bond cleavage of intermediate 1,5-benzodiazepinones under solvent-free conditions." @default.
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• W2425444724 date "2016-07-01" @default.
• W2425444724 modified "2023-10-17" @default.
• W2425444724 title "Selective exploitation of acetoacetate carbonyl groups using imidazolium based ionic liquids: synthesis of 3-oxo-amides and substituted benzimidazoles" @default.
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• W2425444724 doi "https://doi.org/10.1016/j.tetlet.2016.06.048" @default.
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