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• W3166507166 abstract "An efficient and modular strategy was used to obtain enaminones with a wide range of functional groups via a four-component sequential reaction. This reaction proceeded under mild conditions without a catalyst in one pot. Furthermore, the products could be transformed into thiadiazoles." @default.
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• W3166507166 date "2021-06-14" @default.
• W3166507166 modified "2023-10-06" @default.
• W3166507166 title "Synthetic Route to Enaminones via Metal-Free Four-Component Sequential Reactions of Aryl Olefins with CHCl₃, Et₃N, and TBHP" @default.
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• W3166507166 doi "https://doi.org/10.1021/acs.joc.1c00823" @default.
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