An efficient domino approach for the synthesis of multisubstituted pyrroles via gold/silver-catalyzed amination/cycloisomerization of (Z)-2-en-4-yn-1-ols

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Abstract

An efficient and one-pot synthesis of multisubstituted pyrroles with high diversity and in a regioselective manner from the reactions of suitably substituted (Z)-enynols with amines or sulfon-amides under mild reaction conditions has been developed. This synthesis was realized via a cascade process in the presence of gold/silver (Au/Ag) or boron trifluoride·etherate/ gold/silver (BF3·Et2O/Au/Ag) catalysts, which could catalyze amination and cycloisomerization reactions in the same vessel. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.

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Lu, Y., Fu, X., Chen, H., Du, X., Jia, X., & Liu, Y. (2009). An efficient domino approach for the synthesis of multisubstituted pyrroles via gold/silver-catalyzed amination/cycloisomerization of (Z)-2-en-4-yn-1-ols. Advanced Synthesis and Catalysis, 351(1–2), 129–134. https://doi.org/10.1002/adsc.200800490

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