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This document details a one-pot synthesis method for 2H-3-nitrothiochromenes using o-bromobenzaldehydes, sodium sulfide, and β-nitrostyrenes without the need for transition metal catalysts. The method showcases high functional group tolerance and generates thiochromenes with potential biological activities, including anti-inflammatory and anticancer properties. The study emphasizes the simplicity and efficiency of the reaction conditions compared to existing methods, highlighting the use of readily availabl

Author

hai

Language

EN