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- W2968752644 abstract "1-Methyl-3,4-dihydroquinoxalin-2(1H)-one was heated with a range of aldehydes to generate intermediate azomethine ylides which underwent [3 + 2] cycloaddition reactions with N-methyl or N-phenylmaleimide to give substituted tetrahydropyrroloquinoxalinones. Only one (racemic) stereoisomer was formed in each case and the stereochemical outcome was verified by single crystal X-ray analysis. The products from this multicomponent reaction could be oxidised with DDQ to the pyrroloquinoxalinones." @default.
- W2968752644 created "2019-08-22" @default.
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- W2968752644 date "2019-09-01" @default.
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- W2968752644 title "Three-component couplings for the synthesis of pyrroloquinoxalinones by azomethine ylide 1,3-dipolar cycloaddition chemistry" @default.
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- W2968752644 doi "https://doi.org/10.1016/j.tetlet.2019.151023" @default.
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