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• W4383313332 abstract "Elegant synthetic strategies for chromenopyrroles (azacoumestans) have been devised via cycloaddition of 2-hydroxychalcone/cyclic enones and alkyl isocyanoacetate, followed by lactonization. Herein, ethyl isocyanoacetate acts as a C–NH–C–C═O synthon contrary to its hitherto applications as a C–NH–C synthon. Subsequently, pentacyclic-fused pyrroles were also constructed from the o-iodo benzoyl chromenopyrroles using the Pd(II) catalyst." @default.
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• W4383313332 date "2023-07-06" @default.
• W4383313332 modified "2023-10-01" @default.
• W4383313332 title "Synthesis of Chromenopyrroles (Azacoumestans) from Functionalized Enones and Alkyl Isocyanoacetates" @default.
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• W4383313332 doi "https://doi.org/10.1021/acs.orglett.3c01655" @default.
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