Abstract
The sustainable production of industry-relevant chemicals, ranging from biofuels to pharmaceuticals, requires the development of efficient functionalization of biomass-derived building blocks, such as furan derivatives. Herein we report directed iridium-catalyzed C3–H silylation of furfural compounds, which grants access to versatile synthetic platforms. This transformation was developed on furfuryl derivatives, using imines as directing groups, and trialkylsilanes or bis(trimethylsilyl)methylsilane as silylating agents, in the presence of a hydride scavenger. Subsequently, fluoride-mediated activation strategies were applied to the C3–SiMe(OSiMe3)2 furfural derivatives. This strategy enables a wide range of transformations, namely arylation, alkenylation, alkynylation, allylation and alkylation, as well as halogenation and trifluoromethylation. A variety of high value-added products were thus easily obtained from the same common C3-silylated furfural platform.
Supplementary materials
Title
Supporting Information
Description
General information, Further optimizations, Preparation and characterization of starting materials, Preparation and characterization of silylated products, Fluoride-mediated functionalization of C3-SiMe(OTMS)2 furfurals: preparation and characterization of final compounds
1H, 13C and 19F NMR Spectra.
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