This method demonstrates efficient cyclization of benzyl alcohols and acetophenones, indicating practical applications in organic synthesis.
An efficient, facile and one-pot four-component methodology for the cyclization of readily available benzyl alcohols, acetophenones, Meldrum's acid and NH 4 OAc to access dihydropyridinones (valuable scaffolds in medicinal and synthetic organic chemistry) was established. This four-component cyclization reaction supports the straightforward manufacture of several dihydropyridinones. Several C-C and C-N bonds were constructs to synthesize the desired product. Readily available starting, operational simplicity, mild reaction conditions, good to excellent reaction yields, and tolerate various functional groups are the interesting features of this protocol.
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Parveen et al. (2025) studied this question.
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