Gold-catalyzed tandem cycloisomerization of alkynyloxiranes with nucleophiles: An efficient approach to 2,5-disubstituted furans

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Abstract

An efficient approach to 2,5-disubstituted furans has been developed by utilizing gold-catalyzed sequential nucleophilic attack onto metal-complexed alkynes with complete regioselectivity. The reaction proceeds efficiently under mild conditions with commercially available catalysts to afford furans in mod-erate to excellent yields (up to 96 %) with high diversity. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.

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Shu, X. Z., Liu, X. Y., Xiao, H. Q., Ji, K. G., Guo, L. N., Qi, C. Z., & Liang, Y. M. (2007). Gold-catalyzed tandem cycloisomerization of alkynyloxiranes with nucleophiles: An efficient approach to 2,5-disubstituted furans. Advanced Synthesis and Catalysis, 349(16), 2493–2498. https://doi.org/10.1002/adsc.200700319

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