Gold(I)-catalyzed formation of benzo[b]furans from 3-Silyloxy-1,5-enynes

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Abstract

Sport of kings: A new gold(I)-catalyzed transformation has been developed that occurs under mild conditions and proceeds by an expected substituent "castling" (see red and blue circles in scheme) to give efficient access to benzo[b]furans from the easy to obtain 3-silyloxy-1,5-enynes (IPr=N,N′-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, NTf 2=bis(trifluoromethylsulfonylimide). Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Hashmi, A. S. K., Yang, W., & Rominger, F. (2011). Gold(I)-catalyzed formation of benzo[b]furans from 3-Silyloxy-1,5-enynes. Angewandte Chemie - International Edition, 50(25), 5762–5765. https://doi.org/10.1002/anie.201100989

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