Reveals distinct reactivity of thiols in synthesizing valuable chromeno derivatives, suggesting versatile applications.
In this study, an efficient and convenient three/two-component cyclization protocol is presented for the development of synthetically valuable chromeno[2,3‐d]pyrimidine derivatives via pTSA-catalyzed reaction of substituted salicylaldehyde, 1,3-dimethylbarbituric acid, and both...
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Sourabh et al. (2026) studied this question.
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