{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T05:40:52Z","timestamp":1791351652930,"version":"4.3.1"},"reference-count":175,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2012,11,14]],"date-time":"2012-11-14T00:00:00Z","timestamp":1352851200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Chemistry A European J"],"published-print":{"date-parts":[[2013,1,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Nitroacetates and nitroacetamides react in water as in chloroform with electron\u2010deficient 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.<\/jats:p>","DOI":"10.1002\/chem.201202698","type":"journal-article","created":{"date-parts":[[2012,11,14]],"date-time":"2012-11-14T16:37:57Z","timestamp":1352911077000},"page":"665-677","source":"Crossref","is-referenced-by-count":32,"title":["Conjugate Addition versus Cycloaddition\/Condensation of Nitro Compounds in Water: Selectivity, Acid\u2013Base Catalysis, and Induction 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