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• W2970856711 startingPage "6396" @default.
• W2970856711 abstract "A transition-metal-free, redox-neutral, organocatalytic C3-alkenylation of pyrroles is reported. Readily available aldehydes were employed as alkenylating agent and the reaction tolerates several key functional groups. The E-alkenylated products were isolated in moderate to exclusive selectivity. A one-pot two-fold alkenylation strategy is also developed for further downstream modifications. To show the applicability, synthetically challenging indolylpyrrole derivatives were synthesized using Cadogan cyclization." @default.
• W2970856711 created "2019-09-05" @default.
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• W2970856711 date "2019-09-09" @default.
• W2970856711 modified "2023-09-26" @default.
• W2970856711 title "C3-Alkenylation between Pyrroles and Aldehydes Mediated by a Brønsted Acid and a Brønsted Base" @default.
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• W2970856711 doi "https://doi.org/10.1002/ejoc.201901228" @default.
• W2970856711 hasPublicationYear "2019" @default.
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