The preparation of beta-enamino ketones and esters using the methodology of the reactions on solid support coupled with microwave irradiation is described. The reaction of cyclic, acyclic and alpha-chloro-substituted beta-dicarbonyl compounds with amines or their corresponding ammonium acetates was carried out using K-10 as solid support and a domestic microwave oven as the radiation source to give beta-enamino carbonylic compounds in good yields.
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Braibante et al. (2003) studied this question.
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