Abstract
Silver-catalyzed three-component, tandem reactions of 4-alkynyl-2-oxo-2H- chromene-3-carbaldehydes, amines and various nucleophiles result in the formation of highly functionalized chromeno[3,4-c]pyridin-5-ones in high yields. Gold-catalyzed [4+2] cycloadditions of 4-alkynyl-2-oxo-2H-chromene-3- carbaldehydes with alkynes or alkenes have also been achieved to afford benzo[c]chromen-6-ones efficiently. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Xiao, J., Chen, Y., Zhu, S., Wang, L., Xu, L., & Wei, H. (2014). Diversified construction of chromeno[3,4-c]pyridin-5-one and benzo[c]chromen-6-one derivatives by domino reaction of 4-Alkynyl-2-oxo-2H- chromene-3-carbaldehydes. Advanced Synthesis and Catalysis, 356(8), 1835–1845. https://doi.org/10.1002/adsc.201301171
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