Palladium-catalyzed cross-coupling reaction of 4-methylthiazole and 2-trimethylsilylthiazoles with biaryl triflates

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Abstract

2-Trimethylsilylthiazoles serve as an efficient counterpart for direct palladium-catalyzed cross-coupling reaction with aromatic triflates without any fluoride anion source to afford 2-arylthiazoles. © 2006 The Japan Institute of Heterocyclic Chemistry.

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Hara, O., Nakamura, T., Sato, F., Makino, K., & Hamada, Y. (2006). Palladium-catalyzed cross-coupling reaction of 4-methylthiazole and 2-trimethylsilylthiazoles with biaryl triflates. Heterocycles, 68(1), 1–4. https://doi.org/10.3987/com-05-10570

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