. Mhz, 32 (s, 3H), 1.73 (quint CDCl 3 ): ? 147, Hz, 1H), 6.89 (d, J = 3.5 Hz, 1H), 6.59 (d, J = 3.5 Hz, 1H), 1943.

J. =. Mhzt, CDCl 3 ): ? 9.64 (s, 1H), 1H), 7.57 (d, J = 7.5 Hz, 1H), p.47

F. Roger, H. Po?gan, and . Doucet, Palladium-Catalysed Direct Arylation of Heteroaromatics Bearing Unprotected Hydroxyalkyl Functions using Aryl Bromides, Advanced Synthesis & Catalysis, vol.7, issue.4, p.696, 2010.
DOI : 10.1002/adsc.200900793
URL : https://hal.archives-ouvertes.fr/hal-00492621

. Chloropyridine-hydrochloride, 150 g, 1 mmol) and 3-methyl-5-phenylisoxazole (0.239 g, 1.5 mmol) affords 22 in 78% (0.184 g) yield. 1 H NMR (300 MHz, CDCl 3 ) = 126

. Hz, 97 (s, 1 H) 13 C NMR (300 MHz, CDCl 3 ) = 15

J. =. Hzt, 45 (s, 3 H), 4.03 (q, J = 7.2 Hz, 2 H), 2009.

J. =. Hzd, CDCl 3 ) = 15, Hz, 1H). 13 C NMR (300 MHz

J. Hzq and J. =. =d, H) 13 C NMR (300 MHz, CDCl 3 ) = 15, pp.4-24, 2001.

. Hz, 82 (d, J = 7.9 Hz, 1 H) (s, 1 H), pp.4363-4376

Y. Kitamura, S. Sako, A. Tsutsui, Y. Monguchi, T. Maegawa et al., Ligand-Free and Heterogeneous Palladium on Carbon-Catalyzed Hetero-Suzuki-Miyaura Cross-Coupling, Advanced Synthesis & Catalysis, vol.67, issue.4, p.718, 2010.
DOI : 10.1002/adsc.200900638