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- W2092230172 abstract "Tetrasubstituted Pyrroles On the inside cover, N-protected, fully substituted pyrroles are important heteroaromatic compounds in medicinal chemistry and materials science. An efficient one-pot sequential synthesis of a diverse array of N-protected pyrrole 2,4-dicarboxylic acid derivatives is described by Kwunmin Chen and co-workers in their Full Paper on page 330 ff. The synthetic protocol starts from readily available nitroallylic acetates, amines, and a β-keto ester. The reaction is mediated by ceric ammonium nitrate and proceeds smoothly by an interesting SN2′ process and subsequent aromatization." @default.
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- W2092230172 date "2013-04-01" @default.
- W2092230172 modified "2023-10-03" @default.
- W2092230172 title "Inside Cover: Three-component Synthesis of Functionalized<i>N</i>-Protected Tetrasubstituted Pyrroles by an Addition-Elimination-Aromatization Process (Asian J. Org. Chem. 4/2013)" @default.
- W2092230172 doi "https://doi.org/10.1002/ajoc.201390010" @default.
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