Abstract
A versatile solid-phase synthesis of acyl biarylsulfonamides is reported. The synthesis starts with sulfonylation of a solid bound aminomethyl linker group with arylsulfonyl chloride, followed by a Suzuki coupling to construct the biphenyl scaffold. Acylation of the sulfonamide and the proper choice of linker allows the acylsulfonamide to be cleaved as the product. © 2001 Published by Elsevier Science Ltd.
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CITATION STYLE
APA
Xiong, Y., Klopp, J., & Chapman, K. T. (2001). Solid-phase synthesis of acyl biarylsulfonamides. Tetrahedron Letters, 42(48), 8423–8427. https://doi.org/10.1016/S0040-4039(01)01827-5
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