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- W2105704881 endingPage "677" @default.
- W2105704881 startingPage "665" @default.
- W2105704881 abstract "Abstract Nitroacetates and nitroacetamides react in water as in chloroform with electron‐deficient dipolarophiles to give condensation or conjugate addition products under base catalysis. In general, high selectivity towards condensation is observed in water, with shorter induction periods than in chloroform. In water, condensations slowly occur even without base; kinetic profiles evidence the catalytic effect of the base, which should be related to the conversion into the tautomer nitronic acid. Condensations in water provide convenient access to isoxazole derivatives bearing various functional groups including ammonium, carboxy, and carboxyamide." @default.
- W2105704881 created "2016-06-24" @default.
- W2105704881 creator A5029949432 @default.
- W2105704881 creator A5070955159 @default.
- W2105704881 creator A5074952595 @default.
- W2105704881 date "2012-11-14" @default.
- W2105704881 modified "2023-10-18" @default.
- W2105704881 title "Conjugate Addition versus Cycloaddition/Condensation of Nitro Compounds in Water: Selectivity, Acid-Base Catalysis, and Induction Period" @default.
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