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- W3008488178 abstract "Azomethine ylides generated in situ from isatins and α-amino acids undergo smooth 1,3-dipolar cycloaddition with olefins derived from the Baylis–Hillman reaction to produce fused 2-quinolinone derivatives in good yields with high selectivity. The use of microwave irradiation makes this method quite simple and rapid to generate polycyclic frameworks in a single step." @default.
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- W3008488178 date "2020-02-19" @default.
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- W3008488178 title "Microwave accelerated azomethine ylide cycloaddition with Baylis–Hillman adducts" @default.
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