Demonstrates a novel synthesis of thiazole compounds, suggesting efficiency gains over traditional methods.
)-S cross-coupling/intramolecular cyclization/dehydration cascade affording higher yields compared to solution-based traditional methods, which typically require reaction times of several hours. This process features operationally simple mild condition, short reaction time, chemo-/regioselectivity, broad substrate scope, good functional group compatibility, excellent yields, facile scalability, and overcomes key synthetic challenges. Noteworthy, stereochemistry of the exocyclic double bond was assigned to have Z-configuration.
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Kumar et al. (2026) studied this question.
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