Abstract
A variety of arylhydrazonopyridinones were prepared via heating cyanoacetamides with ethyl acetoacetate in absence of solvent under reflux conventionally or ultrasound irradiation or in a microwave oven. The formed products 5 and 6 could be readily converted to thienopyridones. Attempted addition of the latter to electron poor olefins afforded only arylhydrazonopyridinones. © 2008 Elsevier B.V. All rights reserved.
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Al-Zaydi, K. M., Borik, R. M., & Elnagdi, M. H. (2009). Studies with arylhydrazonopyridinones: Synthesis of new arylhydrazono thieno[3,4-c]pyridinones as novel D2T2 dye class; classical verse green methodologies. Ultrasonics Sonochemistry, 16(5), 660–668. https://doi.org/10.1016/j.ultsonch.2008.11.004
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