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1 Discovery of rganic Halides as Regio-Switching xidants Supporting Information Regiodivergent Cross-Dehydrogenative Coupling of Pyridines and Benzoxazoles: Discovery of rganic Halides as Regio-Switching xidants 1 Institute of Transformative Bio-Molecules (WPI-ITbM) and Graduate School of Science, agoya University, Chikusa, agoya , Japan. 2 JST, ERAT, Itami Molecular anocarbon Project, agoya University, Chikusa, agoya , Japan itami@chem.nagoya-u.ac.jp Table of Contents 1. General S2 2. Experimental Procedure S3 3. ptimization of C2-selective Reaction S4 4. Characterization Data for C3-selective Reaction S Characterization Data for C2-selective Reaction S H and 13 C MR Spectra S Validation of reduction of aryl/benzyl bromide S40 43 S1

2 1. General Regiodivergent Cross-Dehydrogenative Coupling of Pyridines and Benzoxazoles: Discovery of rganic Halides as Regio-Switching xidants Unless otherwise noted, all reactants or reagents including dry solvents were obtained from commercial suppliers and used as received. Pd(Ac) 2, dehydrated pyridine, benzyl bromide, 1-bromo-2,4,6-triisopropylbenzene, 4-methylpyridine and benzoxazole were purchased from Wako chemicals. Pd(Piv) 2, 3-methylpyridine and 4-trifluoromethylpyridine were purchased from Sigma-Aldrich. 1,3-Dimesitylimidazolium chloride (IMes HCl) and 3- trifluoromethylpyridine were purchased from TCI. CsPiv S1, substituted benzoxazoles S2, - benzylpyridinium bromide S3 and benzyl pivalate S4 were synthesized according to procedures reported in the literature. Benzyl bromide was freshly purified by vacuum distillation before coupling reaction. Substituted pyridines were used as received. All reactions were performed with dry solvents under an atmosphere of 2 gas in flame-dried glassware using standard vacuum-line techniques. All work-up and purification procedures were carried out with reagent-grade solvents in air. Analytical thin-layer chromatography (TLC) was performed using E. Merck silica gel 60 F254 precoated plates (0.25 mm). The developed chromatogram was analyzed by UV lamp (254 nm) or phosphomolybdic acid/sulfuric acid solution. Flash column chromatography was performed with E. Merck silica gel 60 ( mesh). Silica-gel column chromatography was performed on an Isolera Spektra instrument equipped with a Biotage SAP Ultra 10 g cartridge for 0.25 mmol scale reactions. Preparative recycling gel permeation chromatography (GPC) was performed with a JAI LC-9260 II EXT instrument equipped with JAIGEL- 1H/JAIGEL-2H columns using chloroform as an eluent. uclear magnetic resonance (MR) spectra were recorded on a JEL JM-ECA-600 ( 1 H 600 MHz, 13 C 150 MHz) spectrometer. Chemical shifts for 1 H MR are expressed in parts per million (ppm) relative to tetramethylsilane (δ 0.00 ppm). Chemical shifts for 13 C MR are expressed in ppm relative to CDCl 3 (δ 77.2 ppm). Data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, dd = doublet of doublets, t = triplet, dt = doublet of triplets, q = quartet, m = multiplet), coupling constant (Hz), and integration. S1 Campo, M.; Larock, R. rg. Lett. 2000, 2, S2 Guo, S.; Qian, B.; Xie, Y.; Xia, C.; Huang, H. rg. Lett. 2011, 13, S3 Peng, W.; Zhu, S. J. Chem. Soc. Perkin Trans , S4 Bender, D.; Peterson, J.; McCarthy, J.; Gunaydin, H.; Takano, Y.; Houk, K. rg. Lett. 2008, 10, S2

3 2. Experimental Procedure C3-selective Reaction Regiodivergent Cross-Dehydrogenative Coupling of Pyridines and Benzoxazoles: Discovery of rganic Halides as Regio-Switching xidants The reaction in Figure 2a is representative. A 20-mL Schlenk tube equipped with J. Young -ring tap containing a magnetic stirring bar was dried with a heat gun under reduced pressure and filled with nitrogen gas after cooling to room temperature. To this vessel was added Pd(Ac) 2 (5.6 mg, mmol), and then the tube was introduced into an argonatmosphere glovebox. To the reaction tube was added CsPiv (176 mg, 0.50 mmol) and the tube was taken out from the glovebox. To the tube were added benzoxazole (29.8 mg, 0.25 mmol), 1-bromo-2,4,6-triisopropylbenzene (127 µl, 0.50 mmol) and dry pyridine (1.5 ml) under a stream of nitrogen gas. The vessel was sealed with -ring tap and then stirred at 170 C for 17 h in an 8-well reaction heat block. After cooling to room temperature, the reaction mixture was passed through a short pad of Celite (EtAc was used as an eluent.) The filtrate was concentrated in vacuo. After removal of pyridine, the mixture was purified through silica-gel column chromatography by Isolera Spektra instrument equipped with a Biotage SAP Ultra 10 g cartridge (n-hexane/etac = 19:1 to 3:1) to give 1a (29.0 mg) in 59% yield (C2/C3/C4 = 17:74:9). C2-selective Reaction The reaction of pyridine with benzoxazole in Figure 4 is representative. A 20-mL Schlenk tube equipped with J. Young -ring tap containing a magnetic stirring bar was dried with a heat gun under reduced pressure and filled with nitrogen gas after cooling to room temperature. To this vessel were added Pd(Piv) 2 (7.7 mg, mmol) and IMes HCl (8.5 mg, mmol), and then the tube was introduced into an argon-atmosphere glovebox. To the reaction tube was added CsPiv (176 mg, 0.50 mmol) and the tube was taken out from the glovebox. To the tube were added benzoxazole (29.8 mg, 0.25 mmol), distilled benzyl bromide (59 µl, 0.50 mmol) and dry pyridine (1.5 ml) under a stream of nitrogen gas. The vessel was sealed with -ring tap and then stirred at 170 C for 17 h in an 8-well reaction block. After cooling to room temperature, the reaction mixture was passed through a short pad of Celite (EtAc was used as an eluent). The filtrate was concentrated in vacuo. After removal of pyridine, the mixture was purified through silica-gel column chromatography by Isolera Spektra instrument equipped with a Biotage SAP Ultra 10 g cartridge (nhexane/etac = 19:1 to 3:1) to give 2a (36 mg) in 74% yield. S3

4 3. ptimization of C2-selective Reaction Regiodivergent Cross-Dehydrogenative Coupling of Pyridines and Benzoxazoles: Discovery of rganic Halides as Regio-Switching xidants + Pd source (10 mol%) Ligand (10 mol%) PhCH 2 Br (2 equiv) CsPiv (3 equiv) 170 C, 17 h 1.5 ml 0.25 mmol Entry Pd source Ligand Yield 1 Pd(Ac) 2 SPhos 13% 2 Pd(Ac) 2 5,5 -dimethyl-2,2 -bipyridine 54% 3 Pd(Ac) 2 IMes HCl 64% 4 PdCl 2 IMes HCl 48% 5 Pd(Piv) 2 IMes HCl 74% 6 Pd 2 (dba) 3 CHCl 3 IMes HCl 29% 7 Pd(CH 3 C) 4 (BF 4 ) 2 IMes HCl 25%* 8 PdCl 2 (dppf) CH 2 Cl 2 IMes HCl 0% 9 PEPPSI-IMes none 40% * 1 H MR yield. Benzyl phenyl ether was used as an internal standard. S4

5 Discovery of rganic Halides as Regio-Switching xidants 4. Characterization Data for C3-Selective Reaction 1a = 1a-C3 Major isomer + + 2a 1a-C4 The product 1a (Figure 2b, 33.1 mg, light yellow solid) was obtained as a mixture of regioisomers (1a-C3, 2a, and 1a-C4), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 2-(Pyridin-3-yl)benzo[d]oxazole (1a-C3): 1a-C3 is known compound and showed the identical 1 H MR spectra according to the literature. S5 2-(Pyridin-2-yl)benzo[d]oxazole (2a): 2a is known compound and showed the identical 1 H MR spectra according to the literature. S5 2-(Pyridin-4-yl)benzo[d]oxazole (1a-C4): 1a-C4 is known compound and showed the identical 1 H MR spectra according to the literature. S5 S5 Amaike, K.; Muto, K.; Yamaguchi, J.; Itami, K. J. Am. Chem. Soc. 2012, 134, S5

6 Discovery of rganic Halides as Regio-Switching xidants = + + 1b 1b-C3 Major isomer 1b-C2 1b-C4 The product 1b (Figure 3, 34.0 mg, light yellow solid) was obtained as a mixture of regioisomers (1b-C3, 1b-C2, and 1b-C4), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 5-Methyl-2-(pyridin-3-yl)benzo[d]oxazole (1b-C3): 1b-C3 is known compound and showed the identical 1 H MR spectra according to the literature. S6 5-Methyl-2-(pyridin-2-yl)benzo[d]oxazole (1b-C2): 1b-C2 is known compound and showed the identical 1 H MR spectra according to the literature. S6 5-Methyl-2-(pyridin-4-yl)benzo[d]oxazole (1b-C4): The 1 H MR data was assigned by analogy to compound 1a-C4. 1 H MR (CDCl 3 ) δ 2.49 (s, 3H), (m, 1H), (m, 1H), (m, 1H), 8.06 (d, J = 1.2 Hz, 2H), 8.81 (s, 2H). HR-MS and 13 C MR data for the mixture of 1b-C3, 1b-C2, and 1b-C4: 13 C MR (CDCl 3 ) δ 21.70, , , , , , , , , , , , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. S6 Shen, X.-B.; Zhang, Y.; Chen, W.-X.; Xiao, Z.-K.; Hu, T.-T.; Shao, L.-X. rg. Lett. 2014, 16, S6

7 Discovery of rganic Halides as Regio-Switching xidants Ph Ph Ph = + + Ph 1c 1c-C3 Major isomer 2b 1c-C4 The product 1c (Figure 3, 36.0 mg, light yellow solid) was obtained as a mixture of regioisomers (1c-C3, 2b, and 1c-C4), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 5-Phenyl-2-(pyridin-3-yl)benzo[d]oxazole (1c-C3): The 1 H MR data was assigned by analogy to compound 1a. 1 H MR (CDCl 3 ) δ 7.39 (t, J = 7.2 Hz, 1H), δ (m, 3H), (m, 4H), (m, 1H), 8.54 (dt, J = 7.2, 2.4 Hz, 1H), 8.78 (dd, J = 4.8, 1.8 Hz, 1H), 9.50 (d, J = 1.2 Hz, 1H). 5-Phenyl-2-(pyridin-2-yl)benzo[d]oxazole (2b): The compound data was determined from the pure form of 2b, which was synthesized through the C2-selective reaction. 1 H MR (CDCl 3 ) δ (m, 1H), (m, 3H), 7.64 (d, J = 7.8 Hz, 3H), 7.71 (d, J = 8.4 Hz, 1H), 7.89 (t, J = 1.8 Hz, 1H), 8.02 (s, 1H), 8.38 (d, J = 7.2 Hz, 1H), 8.83 (d, J = 4.2 Hz, 1H); 13 C MR (CDCl 3 ) δ , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 18 H 13 2 : [M + H] + 5-Phenyl-2-(pyridin-4-yl)benzo[d]oxazole (1c-C4): The 1 H MR data was assigned by analogy to compound 1a-C4. 1 H MR (CDCl 3 ) δ 7.39 (t, J = 7.2 Hz, 1H), (m, 3H), (m, 3H), (m, 1H), 8.11 (d, J = 5.4 Hz, 2H), 8.84 (d, J = 5.4 Hz, 2H). 13 C MR data for the mixture of 1c-C3, 2b, and 1c-C4: 13 C MR (CDCl 3 ) δ , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , HR-MS (ESI-MS, positive): m/z = calcd for C 18 H 13 2 : [M + H] +. S7

8 Discovery of rganic Halides as Regio-Switching xidants tbu tbu tbu = + + tbu 1d 1d-C3 Major isomer 2c 1d-C4 The product 1d (Figure 3, 46.7 mg, light yellow solid) was obtained as a mixture of regioisomers (1d-C3, 2c, and 1d-C4), which were inseparable with silica-gel column chromatography or gel-permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 5-(tert-Butyl)-2-(pyridin-3-yl)benzo[d]oxazole (1d-C3): 1d-C3 is known compound and showed the identical 1 H MR spectra according to the literature. S6 5-(tert-Butyl)-2-(pyridin-2-yl)benzo[d]oxazole (2c): 2c is known compound and showed the identical 1 H MR spectra according to the literature. S6 5-(tert-Butyl)-2-(pyridin-4-yl)benzo[d]oxazole (1d-C4): The 1 H MR data was assigned by analogy to compound 1a-C4. 1 H MR (CDCl 3 ) δ 1.41 (s, 9H), (m, 2H), (m, 1H), (m, 2H), 8.81 (d, J = 2.4 Hz, 2H). HR-MS and 13 C MR data for the mixture of 1d-C2, 2c, and 1d-C4: 13 C MR (CDCl 3 ) δ 31.88, 31.94, 35.19, , , , , , , , , , , , , , , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 16 H 17 2 : [M + H] +. S8

9 Discovery of rganic Halides as Regio-Switching xidants Cl Cl Cl = + + Cl 1e 1e-C3 Major isomer 1e-C2 1e-C4 The product 1e (Figure 3, 24.1 mg, white solid) was obtained as a mixture of regioisomers (1e-C3, 1e-C2, and 1e-C4), which were inseparable with silica-gel column chromatography or gel-permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 5-(Chloro)-2-(pyridin-3-yl)benzo[d]oxazole (1e-C3): 1e-C3 is known compound and showed the identical 1 H MR spectra according to the literature. S7 5-(Chloro)-2-(pyridin-2-yl)benzo[d]oxazole (1e-C2): The 1 H MR data was assigned by analogy to compound 2c. 1 H MR (CDCl 3 ) δ (m, 1H), (m, 1H), 7.58 (dd, J = 8.4 Hz, J = 1.8 Hz, 1H), (m, 1H), 7.90 (t, J = 7.8 Hz, 1H), 8.34 (d, J = 7.8 Hz, 1H), 8.82 (d, J = 2.4 Hz, 1H). 5-(Chloro)-2-(pyridin-4-yl)benzo[d]oxazole (1e-C4): The 1 H MR data was assigned by analogy to compound 1a-C4. 1 H MR (CDCl 3 ) δ (m, 1H), (m, 1H), (m, 1H), 8.05 (t, J = 4.8 Hz, 2H), 8.82 (d, J = 2.4 Hz, 2H). HR-MS and 13 C MR data for the mixture of 1e-C3, 1e-C2, and 1e-C4: 13 C MR (CDCl 3 ) δ , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 12 H 8 Cl 2 : [M + H] +. 7 Zhang, W.; Tian, Y.; Zhao,.; Wang, Y.; Li, J.; Wang, Z. Tetrahedron 2014, 70, S9

10 Discovery of rganic Halides as Regio-Switching xidants = + 1f 1f-C3 Major isomer 1f-C2 The product 1f (Figure 3, 31.4 mg, white solid) was obtained as a mixture of regioisomers (1f-C3 and 1f-C2), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 2-(4-Methylpyridin-3-yl)benzo[d]oxazole (1f-C3): 1 H MR (CDCl 3 ) δ 2.83 (s, 3H), 7.27 (d, J = 5.4 Hz, 1H), (m, 2H), 7.61 (d, J = 7.2 Hz, 1H), (m, 2H), 8.57 (d, J = 5.4 Hz, 1H), 9.44 (s, 1H). 2-(4-Methylpyridin-2-yl)benzo[d]oxazole (1f-C2): The authentic product was synthesized with the reported procedure. S8 1 H MR (CDCl 3 ) δ 2.48 (s, 3H), 7.27 (s, 1H), (m, 2H), 7.67 (dd, J = 7.2, 1.8 Hz, 1H), 7.83 (dd, J = 6.6, 2.4 Hz, 1H), 8.22 (s, 1H), 8.67 (d, J = 4.8 Hz, 1H); 13 C MR (CDCl 3 ) δ 21.17, , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. HR-MS and 13 C MR data for the mixture of 1f-C3 and 1f-C2: 13 C MR (CDCl 3 ) δ 21.22, 21.83, , , , , , , , , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. S8 Yan, X.-M.; Mao, X.-R.; Huang, Z.-Z. Heterocycles 2011, 83, S10

11 Discovery of rganic Halides as Regio-Switching xidants = g 1g-C5 Major isomer 1g-C2 1g-C4 The product 1g (Figure 3, 32.7 mg, white solid) was obtained as a mixture of regioisomers (1g-C5, 1g-C2, 1g-C4, and 2f), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 2-(3-Methylpyridin-5-yl)benzo[d]oxazole (1g-C5): The authentic product was synthesized with the reported procedure. S8 1 H MR (CDCl 3 ) δ 2.46 (s, 1H), (m, 2H), (m, 1H), (m, 1H), 8.34 (s, 1H), 8.60 (s, 1H), 9.28 (s, 1H); 13 C MR (CDCl 3 ) δ 18.55, , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. 2-(3-Methylpyridin-2-yl)benzo[d]oxazole (1g-C2): The authentic product was synthesized with the reported procedure. S8 1 H MR (CDCl 3 ) δ 2.88 (s, 3H), (m, 3H), (m, 2H), 7.85 (d, J = 7.2 Hz, 1H), 8.69 (s, 1H); 13 C MR (CDCl 3 ) δ 21.26, , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. 2-(3-Methylpyridin-4-yl)benzo[d]oxazole (1g-C4): The 1 H MR data was assigned by analogy to compound 1a-C4. 1 H MR (CDCl 3 ) δ (m, 1H), (m, 2H), 7.85 (d, J = 8.4 Hz, 1H), 7.04 (d, J = 4.8 Hz, 1H), 8.64 (d, J = 5.4 Hz, 1H), 8.66 (s, 1H). 2-(3-Methylpyridin-6-yl)benzo[d]oxazole (2f): The compound data was determined from the pure form of 2f, which was synthesized through the C2-selective reaction. 1 H MR (CDCl 3 ) δ 2.44 (s, 3H), (m, 2H), 7.66 (dd, J = 5.4, 2.4 Hz, 1H), 7.69 (dd, J = 8.4, 1.8 Hz, 1H), 7.81 (dd, J = 7.2, 1.8 Hz, 1H), 8.25 (d, J = 8.4 Hz, 1H), 8.64 (s, 1H); 13 C MR (CDCl 3 ) δ 18.85, , , , , , 136,10, , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. 2f S11

12 Discovery of rganic Halides as Regio-Switching xidants HR-MS and 13 C MR data for the mixture of 1g-C5, 1g-C2, 1g-C4, and 2f: 13 C MR (CDCl 3 ) δ 18.56, 18.86, 19.23, 21.30, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 11 2 : [M + H] +. S12

13 Discovery of rganic Halides as Regio-Switching xidants F 3 C F 3 C = F 3 C + 1h 1h-C5 Major isomer 1h-C6 The product 1h (Figure 3, 20.1 mg, white solid) was obtained as a mixture of regioisomers (1h-C5 and 1h-C6), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 2-(3-Trifluoromethylpyridin-5-yl)benzo[d]oxazole (1h-C5): 1 H MR (CDCl 3 ) δ (m, 2H), 7.65 (d, J = 7.2 Hz, 1H), 7.83 (d, J = 6.6 Hz, 1H), 8.76 (s, 1H), 9.03 (s, 1H), 9.64 (s, 1H); 13 C MR (CDCl 3 ) δ , , (q, J C-F = 272 Hz), , , , (q, J C-F = 33 Hz), (q, J C-F = 3.0 Hz), , (q, J C-F = 4.4 Hz), , , (3-Trifluoromethylpyridin-6-yl)benzo[d]oxazole (1h-C6): The authentic product was synthesized with the reported procedure. S8 1 H MR (CDCl 3 ) δ (m, 2H), 7.70 (d, J = 7.8 Hz, 1H), 7.87 (d, J = 7.8 Hz, 1H), 8.15 (dd, J = 8.4, 2.4 Hz, 1H), 8.50 (d, J = 8.4 Hz, 1H), 9.07 (s, 1H); 13 C MR (CDCl 3 ) δ , , , (q, J C-F = 272 Hz), , , (q, J C-F = 34 Hz), (q, J C-F = 2.9 Hz), , (q, J C-F = 4.4 Hz), , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 8 F 3 2 : [M + H] +. HR-MS data for the mixture of 1h-C5 and 1h-C6: HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 8 F 3 2 : [M + H] +. S13

14 Discovery of rganic Halides as Regio-Switching xidants tbu tbu F 3 C F 3 C = F 3 C + tbu 1i 1i-C5 Major isomer 1i-C6 The product 1i (Figure 3, 26.4 mg, white solid) was obtained as a mixture of regioisomers (1i- C5 and 1i-C6), which were inseparable with silica-gel column chromatography or gel permeation chromatography. The ratio of regioisomers was determined by 1 H MR spectroscopy. 5-(tert-Butyl)-2-(3-trifluoromethylpyridin-5-yl)benzo[d]oxazole (1i-C5): The 1 H MR data was assigned by analogy to compound 1h. 1 H MR (CDCl 3 ) δ 1.41 (s, 9H), (m, 1H), 7.60 (d, J = 6.6 Hz, 1H), (m, 1H), 8.13 (d, J = 8.4 Hz, 1H), 8.48 (d, J = 8.4 Hz, 1H), 9.05 (s, 1H). 5-(tert-Butyl)-2-(3-trifluoromethylpyridin-6-yl)benzo[d]oxazole (1i-C6): The 1 H MR data was assigned by analogy to compound 1h-C6. 1 H MR (CDCl 3 ) δ 1.41 (s, 9H), (m, 2H), (m, 1H), 8.74 (s, 1H), 9.01 (s, 1H), 9.63 (s, 1H). HR-MS and 13 C MR data for the mixture of 1i-C5 and 1i-C6: 13 C MR (CDCl 3 ) δ 31.89, 35.22, , , , , , (q, J C-F = 271 Hz), (q, J C-F = 270 Hz), , , , (q, J C-F = 35 Hz), (q, J C-F = 33 Hz), (q, J C-F = 4.4 Hz), , , , (q, J C-F = 4.4 Hz), (q, J C-F = 2.9 Hz), , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 17 H 16 F 3 2 : [M + H] +. S14

15 Discovery of rganic Halides as Regio-Switching xidants 1j 5-(tert-Butyl)-2-(2,6-dimethylpyridin-3-yl)benzo[d]oxazole: (Figure 3, 20.2 mg, colorless liquid) 1 H MR (CDCl 3 ) δ 1.41 (s, 9H), 2.61 (s, 1H), 3.03 (s, 1H), 7.15 (d, J = 8.4 Hz, 1H), 7.43 (dd, J = 8.4, 1.2 Hz, 1H), 7.50 (d, J = 8.4 Hz, 1H), 7.83 (d, J = 1.2 Hz, 1H), 8.32 (d, J = 7.8 Hz, 1H); 13 C MR (CDCl 3 ) δ 24.86, 25.38, 31.97, 35.16, , , , , , , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 18 H 21 2 : [M + H] +. S15

16 Discovery of rganic Halides as Regio-Switching xidants 5. Characterization Data for C2-Selective Reaction 2a 2-(Pyridin-2-yl)benzo[d]oxazole (2a): (Figure 4, 36.3 mg, white solid) The compound data for 2a was presented in the C3-selective reaction section (vide supra). Ph 2b 5-Phenyl-2-(pyridin-2-yl)benzo[d]oxazole (2b): (Figure 4, 29.3 mg, light yellow solid) The compound data for 2b was presented in the C3-selective reaction section (vide supra). tbu 2c 5-(tert-Butyl)-2-(pyridin-2-yl)benzo[d]oxazole (2c): (Figure 4, 30.2 mg, white solid) The compound data for 2c was presented in the C3-selective reaction section (vide supra). Me 2d 5-Methoxy-2-(pyridin-2-yl)benzo[d]oxazole (2d): (Figure 4, 35.7 mg, white solid) 1 H MR (CDCl 3 ) δ 3.89 (s, 3H), 7.02 (d, J = 9.0 Hz, 1H), 7.29 (s, 1H), 7.45 (t, J = 6.6 Hz, 1H), 7.55 (dd, J = 9.0, 1.8 Hz, 1H), 7.89 (t, J = 7.8 Hz, 1H), 8.34 (d, J = 8.4 Hz, 1H), 8.82 (d, J = 4.8 Hz, 1H); 13 C MR (CDCl 3 ) δ 56.16, , , , , , , , S16

17 Discovery of rganic Halides as Regio-Switching xidants , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H : [M + H] +. CF 3 2e 2-(4-Trifluoromethylpyridin-2-yl)benzo[d]oxazole (2e): (Figure 4, 14.8 mg, white solid) 1 H MR (CDCl 3 ) δ (m, 2H), (m, 2H), 7.87 (d, J = 7.2 Hz, 1H), 8.61 (s, 1H), 9.01 (d, J = 4.8 Hz, 1H); 13 C MR (CDCl 3 ) δ , (q, J C-F = 2.9 Hz), (q, J C-F = 4.4 Hz), , (q, J C-F = 271 Hz), , , (q, J C-F = 35 Hz), , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 13 H 8 F 3 2 : [M + H] +. 2f 2-(5-Methylpyridin-2-yl)benzo[d]oxazole (2f): (Figure 4, 19.9 mg, white solid) The compound data for 2f was presented in the C3-selective reaction section (vide supra). Me 2g 5-Methoxy-2-(5-methylpyridin-2-yl)benzo[d]oxazole (2g): (Figure 4, 23.3 mg, pale glay solid) 1 H MR (CDCl 3 ) δ 2.45 (s, 1H), 3.88 (s, 1H), 7.00 (dd, J = 9.0, 2.4 Hz, 1H), 7.28 (d, J = 1.8 Hz, 1H), 7.53 (d, J = 9.0 Hz, 1H), 7.69 (d, J = 7.8 Hz, 1H), 8.23 (d, J = 8.4 Hz, 1H), 8.63 (s, 1H); 13 C MR (CDCl 3 ) δ 18.84, 56.16, , , , , , S17

18 Discovery of rganic Halides as Regio-Switching xidants , , , , , , ; HR-MS (ESI-MS, positive): m/z = calcd for C 14 H : [M + H] +. S18

19 6. 1 H and 13 C MR Spectra Regiodivergent Cross-Dehydrogenative Coupling of Pyridines and Benzoxazoles: Discovery of rganic Halides as Regio-Switching xidants Figure S 1. 1 H MR spectrum of 1a (C2/C3/C4 = 17:74:9). Figure S C MR spectrum of 1a (C2/C3/C4 = 17:74:9). S19

20 Discovery of rganic Halides as Regio-Switching xidants Figure S 3. 1 H MR spectrum of 1b (C2/C3/C4 = 20:65:8). Figure S C MR spectrum of 1b (C2/C3/C4 = 20:65:8). S20

21 Discovery of rganic Halides as Regio-Switching xidants Ph Figure S 5. 1 H MR spectrum of 1c (C2/C3/C4 = 18:73:9). Ph Figure S C MR spectrum of 1c (C2/C3/C4 = 18:73:9). S21

22 Discovery of rganic Halides as Regio-Switching xidants t-bu Figure S 7. 1 H MR spectrum of 1d (C2/C3/C4 = 21:69:10). t-bu Figure S C MR spectrum of 1d (C2/C3/C4 = 21:69:10). S22

23 Discovery of rganic Halides as Regio-Switching xidants Cl Figure S 9. 1 H MR spectrum of 1e (C2/C3/C4 = 27:65:8). Cl Figure S C MR spectrum of 1e (C2/C3/C4 = 27:65:8). S23

24 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 1f (C2/C3 = 33:67). Figure S C MR spectrum of 1f (C2/C3 = 33:67). S24

25 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 1g (C2/C4/C5/C6 = 14:14:51:21). Figure S C MR spectrum of 1g (C2/C4/C5/C6 = 14:14:51:21). S25

26 Discovery of rganic Halides as Regio-Switching xidants F 3 C Figure S H MR spectrum of 1h (C5/C6 = 63:37). F 3 C Figure S C MR spectrum of 1h (C5/C6 = 63:37). S26

27 Discovery of rganic Halides as Regio-Switching xidants F 3 C Figure S H MR spectrum of 1i (C5/C6 = 67:33). F 3 C Figure S C MR spectrum of 1i (C5/C6 = 67:33). S27

28 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 1j. Figure S C MR spectrum of 1j. S28

29 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 2a. Figure S C MR spectrum of 2a. S29

30 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 2b. Figure S C MR spectrum of 2b. S30

31 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 2c. Figure S C MR spectrum of 2c. S31

32 Discovery of rganic Halides as Regio-Switching xidants Me Figure S H MR spectrum of 2d. Me Figure S C MR spectrum of 2d. S32

33 Discovery of rganic Halides as Regio-Switching xidants CF 3 Figure S H MR spectrum of 2e. CF 3 Figure S C MR spectrum of 2e. S33

34 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of 2f. Figure S C MR spectrum of 2f. S34

35 Discovery of rganic Halides as Regio-Switching xidants Me Figure S H MR spectrum of 2g. Me Figure S C MR spectrum of 2g. S35

36 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of authentic 1f-C2. Figure S C MR spectrum of authentic 1f-C2. S36

37 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of authentic 1g-C5. Figure S C MR spectrum of authentic 1g-C5. S37

38 Discovery of rganic Halides as Regio-Switching xidants Figure S H MR spectrum of authentic 1g-C2. Figure S C MR spectrum of authentic 1g-C2. S38

39 Discovery of rganic Halides as Regio-Switching xidants F 3 C Figure S H MR spectrum of authentic 1h-C6. F 3 C Figure S C MR spectrum of authentic 1h-C6. S39

40 Discovery of rganic Halides as Regio-Switching xidants 7. Validation of reduction of aryl/benzyl bromide Mesityl bromide was reduced to mesitylene during the reaction. Mesitylene was observed by 1 H MR in the crude mixture after evaporation of pyridine. H + Pd(Ac) 2 (10 mol %) MesBr (2.0 equiv) CsPiv (3.0 equiv) 170 C, 17 h 1.5 ml 0.25 mmol 1a (68% yield) C3 + MesBr = Br 74% C3 selectivity (C2/C3/C4 = 19:72:9) abundance Br Me H Me X : parts per Million : Proton Figure S H MR spectrum of authentic mesityl bromide. S40

41 Discovery of rganic Halides as Regio-Switching xidants abundance Me H X : parts per Million : Proton Figure S H MR spectrum of authentic mesitylene. Me Br abundance abundance X : parts per Million : Proton Me Me X : parts per Million : Proton Figure S H MR spectrum of crude reaction mixture of the reaction. S41

42 Discovery of rganic Halides as Regio-Switching xidants Benzyl bromide was also reduced to toluene during the reaction. Toluene was detected by GC-MS in the crude mixture. H + Pd(Piv) 2 (10 mo l%) IMes HCl (10 mol %) PhCH 2 Br (2.0 equiv) CsPiv (3.0 equiv) 170 C, 17 h ml 0.25 mmol 2a: 74% Full-scale GC spectra Inset ( min) GC spectra Figure S 46. Full-scale and inset ( min) to GC-MS spectra of the crude mixture. S42

43 Discovery of rganic Halides as Regio-Switching xidants Full-scale MS spectra Figure S 47. Full-scale and inset MS spectra at min. Inset MS spectra S43