, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (1.2 g, 89%) after a chromatography over silica gel (cyclohexane-ethyl acetate 95/5 to 9/1). 1 H NMR (CDCl3): 8.43 (s, 1H), 7.97 (m, 2H), 7.48 (m, 2H), 7.40 -7.24 (m, 7H), 6.96 (m, 1H), 5.96 (m, 1H), 5.00 (m, 1H), 4.93 (m, 1H)

1. and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.51 g, 80%) after a chromatography over silica gel (cyclohexane-ethyl acetate 95:5). 1 H NMR (CDCl3): 8.42 (s, 1H), 8.00 -7.89 (m, 2H), 7.50 -7.42 (m, 2H), 7.40 -7.32 (m, 1H), 7.32 -7.26 (m, 3H), 7.26 -7.21 (m, 2H)

1. and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a yellow oil (0.69 g, 74%) after a chromatography over silica gel (dichloromethane). 1 H NMR (CDCl3): 8.38 (s, 1H), 7.96 -7.89 (m, 2H), 7.48 -7.40 (m, 2H), 7.38 -7.26 (m, 5H), 7.25 -7.19 (m, 1H), 5.83 -5.77 (m, 1H), 5.72 (d, 1H, J = 3.0 Hz), vol.5

E. Nield, R. Stephens, and J. C. Tatlow, 30. Fluorocyclohexanes. Part V. 1H : 4H/2H : 5H-, 1H : 5H/-2H : 4H-, 1H : 2H/4H : 5H-, and 1H : 2H : 4H/5H-octafluorocyclohexane and derived compounds, Journal of the Chemical Society (Resumed), vol.1, issue.3, p.159, 1959.

. Hz, Figure 5?figure supplement 4. 1H NMR (500 MHz, MeOD; upper panel) and 13C NMR (150 MHz, MeOD; lower panel) of compound 4, 2-((E)-prop-1-en-1-yl)maleic acid., 1.91 (s, 3H), 1.24 (d, 3H J = 7.0 Hz), 1.20 (d, 3H J = 6.5 Hz). 13 C NMR

3. Hz-;-t and J. =. , Figure 5?figure supplement 4. 1H NMR (500 MHz, MeOD; upper panel) and 13C NMR (150 MHz, MeOD; lower panel) of compound 4, 2-((E)-prop-1-en-1-yl)maleic acid., 13 C NMR (CDCl3): 171.9

M. L. Dennis and T. S. Peat, WDR5delta32 bound to ethyl 3-(4-(hydroxymethyl)-1H-imidazol-2-yl)propanoate, H NMR (CDCl3): 8.44 (s, 1H), 7.97 (m, 2H), 7.47 (m, 2H), 7.37 (m, 1H), vol.1, pp.33-40, 2019.

1. Hz-;-d and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 4.96 (m, 1H), 4.15 (m, 4H), vol.3

, 23S-Ethyl-24-methylenecycloartan-3?-yl Acetate, Natural Compounds, pp.182-182, 2013.

H. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., CDCl3): 8.42 (s, 1H), 7.95 (m, 2H), 7.47 (m, 2H), 7.36 (m, 1H), 7.28 (m, 5H), vol.6

. Hz,

E. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.41 g, 89%) after a chromatography over silica gel (cyclohexane-ethyl acetate 95:5). 1 H NMR (CDCl3): 8.43 (s, 1H), 7.97 (m, 2H), 7.48 (m, 2H), 7.37 (m, 1H), 7.21 (m, 4H), 7.08-6.96 (m, 4H), 4.97 (m, 2H), 4.14 (m, 4H), 3.17 (dd, 1H, J = 5.0, 13.7 Hz), 3.07 (dd, 1H, J = 5.7, 13.7 Hz), vol.12, pp.1-31068

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.35 g, 75%) after a chromatography over silica gel (cyclohexane-ethyl acetate 95:5). 1 H NMR (CDCl3): 8.42 (s, 1H), 7.96 (m, 2H), 7.48 (m, 2H), 7.38 (m, 1H), 7.21 (m, 2H), 7.08 (m, 3H), 6.22 (dd, 1H, J = 2.0, 3.3 Hz), 5.83 (m, 1H), 5.16 (d (br), 1H, J = 7.6 Hz), 4.96 (m, 1H), 4.17 (m, 4H), vol.12, pp.31068-31091

E. L. Altschuler, The first case of sarcoidosis treated with mycophenolate mofetil, British Journal of Dermatology, vol.149, issue.2, pp.442-442, 2003.

;. Ethyl and J. =. 1h, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.1 g, 28%) after a chromatography over silica gel (cyclohexane-ethyl acetate 96:4). 1 H NMR (CDCl3): 8.37 (s, 1H), 7.97 (m, 2H), 7.47 (m, 2H), 7.37 (m, 2H), 7.21 (m, 4H), 7.02 (m, 2H), 6.93 (m, 1H), 6.85 (m, 1H), 6.03 (d(br), vol.14, pp.31070-111

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.45 (s, 1H), 7.93 (m, 2H), 7.48 (m, 2H), 7, vol.22

3. Hz-;-t and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.45 (s, 1H), 7.93 (m, 2H), 7.47 (m, 2H), 7.38 (m, 1H), 6.79 (m, 2H), 6.70 (m, 1H), 5.83, vol.22, pp.44-32712

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.22, issue.3, p.5493, 1965.

. Hz, Figure 2. Point of subjective equality (PSE) obtained using two interval forced choice paradigm.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.25 g, 64%), using toluene at 90 °C, after a chromatography over silica gel (cyclohexane -ethyl acetate 96/4). 1 H NMR (CDCl3): 8.43 (s, 1H), 7.90 (m, 2H), 7.45 (m, 2H), 7.36 (m, 1H), 7.05 (m, 1H), 6.94 (m, 2H), 5.77 (s, 1H), 5.22 (d, 1H, J = 7.5 Hz), 4.95 (dt, 1H, J = 7.5, 5.5 Hz

E. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.37 g, 82%), using toluene at 90 °C, after a chromatography over silica gel (cyclohexane -ethyl acetate 97/3 to 96/4). 1 H NMR (CDCl3): 7.91 (s, 1H), 7.90 (m, 2H), 7.45 (m, 2H), 7.35 (m, 1H), 7.24 (m, 3H), 7.07 (m, 3H), 6.95 (m, 1H), 5.02 (m, 2H), vol.24, pp.1-33067

. Hz, Figure 2. Point of subjective equality (PSE) obtained using two interval forced choice paradigm., 124.1 (4 and 6 Hz), vol.115

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.44 (s, 1H), 7.91 (m, 2H), 7.45 (m, 2H), 7.37 (m, 1H), 7.29 (dd, 1H, J = 1.9, 0.8 Hz), 7.08 (m, 1H), 7.00 (m, 2H), vol.24, pp.31095-125

. Hz, 13 C NMR (CDCl3): 171.9, 150.6 (248, 13 Hz), 150.5, 150.1, 148.9, vol.126

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.43 (s, 1H), 7.90 (m, 2H), 7.45 (dd, 2H, J = 8.3, 6.9 Hz), 7.36 (m, 1H), 7.07 (m, 1H), 7.00 (m, 2H), vol.24, p.3

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1.

C. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.43 (s, 1H), 7.89 (m, 2H), 7.44 (m, 2H), 7.36 (m, 1H), 7.07 (m, 1H), 7.00 (m, 2H), 5.86 (m, 2H), 5.17 (d, 1H, J = 7.6 Hz, vol.126

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.21 g, 46%), using toluene at 60 °C, after a chromatography over silica gel (cyclohexane -ethyl acetate 96/4). 1 H NMR (CDCl3): 8.43 (s, 1H), 7.89 (m, 2H), 7.44 (m, 2H), 7.36 (m, 1H), 7.08 (m, 1H), 7.00 (m, 2H), 5.77 (s, 1H), 5.20 (d, 1H, J = 7.6 Hz), 4.95 (dt, 1H, J = 7.6, 5.4 Hz), 4.21 (m, 4H), 3.18 (d, 2H, J = 5.4 Hz), 2.13 (s, 3H), 1.88 (s, 3H), 1.27 (t, 3H, J = 7.1 Hz). 13 C NMR, vol.126

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., J = 7.8 Hz), 4.99 (m, 1H), 4.22 (m, 4H), 3.21 (m, 2H), 2.94 (sept, 1H, J = 7.1), 1.91 (s, 3H), 1.28 (d, 3H J = 7.0 Hz), 1.19 (d, 3H J = 7.1 Hz), 1.18 (d, 3H J = 7.1 Hz). 13 C NMR, vol.24, pp.52-33069

E. , Pyridinium, 1-Ethyl-3-(p-(p-((p-(1-Ethyl-Pyridinium-3-yl)Phenyl)Carbamoyl)-Cinnamamido)Phenyl)-Di-p-Toluene Sulfonate 20302-25-4, vol.3, 2004.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., /3 to 96/4). 1 H NMR (CDCl3): 8.46 (s, 1H), 7.89 (m, 2H), 7.45 (m, 2H), 7.36 (m, 1H), 7.26 (m, 3H), 7.08 (m, 2H), 6.83 (m, 1H), 6.69 (m, 1H), 5.03 (m, 1H), 4.90 (d (br), J = 7.3 Hz), 4.20 (q, 2H, J = 7.1 Hz), 4.08 (m, 2H), 3.29 (dd, 1H, J = 5.6 and 13.8 Hz), 3.18 (dd, 1H, J = 6.3 and 13.8 Hz), vol.1, p.28

. Hz,

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 8.45 (s, 1H), 7.91 (m, 2H), 7.47 (m, 2H), 7.35 (m, 1H), 7.29 (m, 1H), 6.87 (m, 1H), 6.74 (m, 1H), 6, vol.3, p.12

. Hz, 150.5, 150.2 (247, 13 and 15 Hz), vol.145

E. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.28 g, 62%) after a chromatography over silica gel (cyclohexane-ethyl acetate 2/1). 1 H NMR (CDCl3): 8.52 (m, 3H), 8.44 (s, 1H), 7.90 (m, 2H), 7.46 (m, 3H), 7.35 (m, 1H), 7.26 (m, 3H), 7.19 (ddd, 1H, J = 0.9, 4.9, 5.6 Hz), 7.03 (m, 2H), 5.01 (m, 1H), vol.35, pp.1-30367

E. , 1 H NMR (CDCl3; 1/1 mixture of diastereoisomers): 8.34 (s, 0.5H), 8.33 (s, 0.5H), .84 (m, 2H), 7.45 -7.40 (m, 2H), 7.35 -7.21 (m, 6H), 6.62 (d, 0.5H, J = 7.5 Hz), vol.38, pp.89-96

. Hz, International Politics, vol.38, issue.1, pp.137-141, 2001.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., /1). 1 H NMR (CDCl3): 8.37 (s, 1H), 7.91 (m, 2H), 7.45 (m, 2H,), 7.25-7.37 (m, 4H), 7.20 (m, 2H), 4.99-5.10 (m, 2H), 4.89 (m, 2H), 3.29 (q, 1H, J = 13.8 Hz), 3.27 (q, 1H, J = 13.6 Hz), vol.2

L. Damodharan, V. Pattabhi, M. Behera, and S. Kotha, Optimization of interactions in crystal packing revealed by crystal structures [ethyl 2-(formylamino)-3-thien-2-yl-2-(thien-2-ylmethyl)propanoate and ethyl 3-(5-bromothien-2-yl)-2-[(5-bromothien-2-yl)methyl]-2-(formylamino)propanoate], Journal of Molecular Structure, vol.705, issue.1-3, pp.101-106, 2004.

H. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 1H, J = 7.5 Hz), 4.95 (m, 1H), 4.18 (m, 4H), 3.15 (d, 2H, J = 5.3 Hz), 2.58 (q, 2H, J = 7.6 Hz), 1.24 (t, 3H, J = 7.2 Hz), 1.21 (t, 3H, J = 7.6 Hz). 13 C NMR (CDCl3): 172.0, 160.1 (248 Hz), vol.5, p.48

J. 1h, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.48 g, 86%) after a chromatography over silica gel (cyclohexane -ethyl acetate 95/5). 1 H NMR (CDCl3): 8.51 (d, 1H, J = 2.4 Hz), 8.02 (dt, 1H, J = 1.9, 7.8 Hz), 7.35-7.23 (m, 7H), vol.7, pp.30367-171

. Hz, Figure 2. Point of subjective equality (PSE) obtained using two interval forced choice paradigm., vol.124

1. and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 1 H NMR (CDCl3): 8.53 (d, 1H, J = 2.3 Hz), 8.00 (td, 1H, J = 7.8, 1.9 Hz), 7.33 (m, 1H), 7.26 (m, 2H), 7.16 (m, 1H), 7.06 (dd, 1H, J = 7.6, 0.6 Hz), 6.96 (m, 2H), 5.82 (m, 1H), 5.77 (d, 1H, J = 3.0 Hz), vol.3, pp.42-31095

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid (0.13 g, 57%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.92 (m, 2H), 7.81 (s, 1H), 7.63 (m, 2H), 7.47 (m, 2H), 7.40 (m, 1H), 7.33 -7.22 (m, 4H), 7.06 (m, 2H), 6.95 (m, 1H), vol.115

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a beige solid (0.31 g, 70%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.94 -7.86 (m, 2H), 7.79 (s, 1H), 7.65 -7.58 (m, 2H), 7.50 -7.36 (m, 3H), 7.35 -7.17 (m, 5H), 7.00 (dd, 2H, J = 9, vol.8

C. Nmr, HRMS (m/z): [M+H] + calcd for C28H23ClN3O2, 468.1479; found, 468.1485. 8-Benzyl-6-phenyl-2-(2-(trifluoromethyl)benzyl)imidazo[1,2-a]pyrazin-3-yl acetate 25{1, Obtained as a white solid (0.23 g, 62%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.92 (m, 2H), 7.81 (s, 1H), 7.62 (m, 2H), 7.48 (m, 2H), 7.40 (m, 1H), 7.28 (m, 7H), 4.63 (s, 2H), 4.14 (s, 2H), vol.2

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.08 g, 57%). 1 H NMR (CDCl3): 7.91 (m, 2H), 7.81 (s, 1H), 7.63 (m, 3H), 7.54-7.38 (m, 6H), vol.124

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.08 g, 66%). 1 H NMR (CDCl3): 7.92 (m, 2H), 7.81 (s, 1H), 7.60 (m, 4H), 7.49-7.38 (m, 5H), vol.7, pp.33-40

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), issue.2, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.160, issue.6, p.5493, 1965.

. Hz, 111.1 (3 and 21 Hz), vol.108

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, issue.6, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.7, issue.2, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), issue.6, p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid (0.37 g, 73%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.92 -7.87 (m, 2H), 7.80 (s, 1H), 7.65 -7.58 (m, 2H), 7.49 -7.42 (m, 2H), 7.42 -7.34 (m, 1H), 7.34 -7.27 (m, 2H), 7.25 -7.20 (m, 1H), 7.19 (dd, 1H, J = 5.1, 1.3 Hz), 6.95 (dd, 1H, J = 5.1, 3.5 Hz), 6.93 -6.88 (m, 1H)

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.6, issue.73, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

Y. Wang and Z. M. Zhang, Crystal structure of TRKc in complex with 3-((6-(4-aminophenyl)imidazo[1,2-a]pyrazin-3-yl)ethynyl)- N-(3-isopropyl-5-((4-methylpiperazin-1-yl)methyl)phenyl)-2- methylbenzamide, vol.1, pp.45-32712, 2019.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.6, p.5493, 1965.

. Hz,

;. Hz and . Nmr, § 126?§ 128, Handelsgesetzbuch, Band 3, §§ 105-160

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, issue.86, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.25, issue.1, p.5493, 1965.

C. Nmr, Coming events, Optics & Laser Technology, vol.23, issue.2, pp.126-128, 1991.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

, Chemical structure 3. tert-butyl 2-((2,6-dimethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)(methyl)amino)acetate., vol.1

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

C. Nmr, Boiler explosion, Journal of the Franklin Institute, vol.108, issue.2, pp.126-128, 1879.

H. Nmr, 2-ISOPROPYL-5-METHYL-2-HEXENE-1-YL ACETATE, Monographs on Fragrance Raw Materials, vol.1, p.468, 1979.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

;. Hz and . Nmr, Oudheid, Tijdschrift voor geschiedenis, vol.133, issue.1, pp.126-128, 2020.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.7, issue.10, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, issue.3, p.5493, 1965.

C. Nmr, HRMS (m/z): [M+H] + calcd for C27H25N4O3: 453.1927; found, 453.1938. 8-Benzyl-2-((5-methyloxazol-2-yl)methyl)-6-phenylimidazo[1,2-a]pyrazin-3-yl acetate 25{1,1,58} (YJ 31776-096-2): Obtained as a white solid (0.01 g, 1.6% from 3-benzyl-2-chloro-5-phenylpyrazine) after a chromatography over silica gel (cyclohexane -ethyl acetate 1/1) and a recrystallization from cyclohexane, Obtained as a white solid (0.12 g, 41%) after recrystallization in n-heptane. 1 H NMR (CDCl3): 7.93 (m, 2H), 7.86 (s, 1H), 7.61 (m, 2H), 7.48 (m, 2H), 7.42 (m, 1H), 7.32 (m, 2H), 7.25 (m, 1H), vol.5

U. Willinger, M. Schmoeger, C. Mueller, and E. Auff, Theory of mind & cognitive flexibility, European Psychiatry, vol.26, issue.S2, pp.439-439, 2011.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.60, p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid (0.12 g, 61%) after a recrystallization in n-heptane. 1 H NMR (CDCl3): 7.86-7.83 (m, 3H), 7.52-7.48 (dt, 1H, J = 7.4, 1.9 Hz), 7.47-7.23 (m, 8H)

. Hz, GÉNÉALOGIES ET RÉPERTOIRE, Correspondance 1774?1792, pp.435-452, 1993.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.18 g, 58%). 1 H NMR (CDCl3): 7.84 (m, 2H), 7.83 (s, 1H), 7.50 (m, 1H), 7.42 (m, 2H), 7.36 (m, 1H), 7.23 (m, 2H), 7.13-7.06 (m, 5H), vol.123, p.466

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.26 g, 87%). 1 H NMR (CDCl3): 7.85 (m, 2H), 7.83 (s, 1H), 7.48 (m, 1H), 7.42 (m, 2H), 7.36 (m, 1H), 7.25 (m, 2H), 7.10 (m, 2H), 6.90 (m, 2H), 6.81 (m, 1H), vol.123

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.19 g, 73%). 1 H NMR (CDCl3): 7.87 (s, 1H), 7.85 (m, 2H), 7.50-7.34 (m, 5H), 7.24 (m, 1H), 7.10 (m, 2H), vol.2, pp.31070-051

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., vol.2, pp.115-116

. Hz, Hz), 27.2, 20.1 (one signal missing). HRMS (m/z): [M+H] + calcd for C26H21FN3O3, 442.1567, found, vol.32, pp.442-1567

, -methylfuran-2-yl)methyl)-6-phenylimidazo[1,2-a]pyrazin-3-yl acetate 25{1,2,42} (YJ31070-053-1): Obtained as a white solid after a recrystallization

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 87 (s, 1H), 7.85 (m, 2H), 7.50-7.34 (m, 4H), 7.24 (m, 1H), 7.10 (m, 2H), vol.6

. Hz, Figure 5?figure supplement 4. 1H NMR (500 MHz, MeOD; upper panel) and 13C NMR (150 MHz, MeOD; lower panel) of compound 4, 2-((E)-prop-1-en-1-yl)maleic acid., vol.115

J. 3h, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 87 (s, 1H), 7.85 (m, 2H), 7.50-7.34 (m, 4H), 7.24 (m, 1H), 7.10 (m, 2H), 6.04 (d, 1H, J = 3.1 Hz), 5.92 (m, 1H), 4.70 (s, 2H), vol.4

C. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 87 (s, 1H), 7.85 (m, 2H), 7.43 (m, 4H), 7.25 (m, 1H), 7.10 (m, 2H), 5.93 (s, 1H), 4.70 (s, 2H), 4.15 (s, 2H), vol.2

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.19 g, 50%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.90 (m, 2H), 7.82 (s, 1H), 7.47 (m, 2H), 7.42 -7.25 (m, 9H), 6.95 (m, 1H), vol.116

A. Jha, Unusual synthesis of 1-(4-fluorobenzyl)-N-(1-(1-(4-fluorobenzyl)-6-isopropoxy-1H-benzo[d]imidazol-2-yl)piperidin-4-yl)-6-isopropoxy-1H-benzo[d]imidazol-2-amine, Arkivoc, vol.2006, issue.1, pp.13-20, 2005.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.161, issue.7, p.5493, 1965.

. Hz, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., pp.116-122

. Hz, HZ 21, The Hundred Greatest Stars, vol.115, pp.104-105

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), issue.2, p.5493, 1965.

. Hz, HZ 21, The Hundred Greatest Stars, vol.113, pp.104-105

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid after a recrystallization in n-heptane (0.12 g, 60%). 1 H NMR (CDCl3): 7.90 (m, 2H), 7.82 (s, 1H), 7.47 (m, 2H), 7.38 (m, 3H), 7.26 (m, 1H), 6.95 (m, 3H), 6.80 (m, 1H)

. Hz,

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.13 g, 59%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.91 (m, 2H), 7.85 (s, 1H), 7.49 (m, 2H), 7.42 -7.33 (m, 4H), 7.26 (m, 1H), 6.93 (m, 1H), vol.6, pp.116-122

. Hz, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., vol.113

M. A. Convery, InhA (T2A mutant) complexed with 5-((5-Amino-3-methyl-1H-pyrazol-1-yl)methyl)-N-(1-(2-chloro-6-fluorobenzyl)-1H-pyrazol-3-yl)-1,3,4-thiadiazol-2-amine, vol.3, 2018.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 7.85 (s, 1H), 7.47 (m, 2H), 7.42 -7.24 (m, 4H), 6.92 (m, 1H), 6.03 (d, 1H, J = 3.0 Hz), 5.91 (m, 1H), pp.116-122

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., vol.113

M. A. Convery, InhA (T2A mutant) complexed with 5-((5-Amino-3-methyl-1H-pyrazol-1-yl)methyl)-N-(1-(2-chloro-6-fluorobenzyl)-1H-pyrazol-3-yl)-1,3,4-thiadiazol-2-amine, vol.3, 2018.

2. Hz-;-q and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Hz), vol.2, issue.6

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid in two crops (0.04 g, 33%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.90 (m, 2H), 7.81 (s, 1H), 7.58 (m, 2H), 7.47 (m, 2H), 7.40 (m, 1H), 7.36 -7.24 (m, 5H), 7.00 (m, 2H), vol.131

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.28 g, 95%) after dispertion of the reaction media in water, a filtration and drying under vacuum at 40°C. 1 H NMR (CDCl3): 7.91 (m, 2H), 7.85 (s, 1H), 7.57 (m, 2H), 7.47 (m, 2H), 7.40 (m, 2H), 7.00 (m, 2H), 6.36 (m, 1H), 6.16 (m, 1H), pp.37-31776

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.126, issue.5, p.5493, 1965.

C. Nmr, Eleven Psalms lamma(alot: 121, 124, 125, 126, 127, 128, 129, 131, 132, 133, 134, Major Poems of the Hebrew Bible, pp.271-305, 2003.

, Obtained as a solid (0.03 g, 27%) after a recrystallization in n-heptane. 1 H NMR (CDCl3): 7.88 (s, 1H), 7.83 (m, 2H), 7.46-7.33 (m, 5H), 7.21 (m, 2H), 6.04 (m, 1H), 5.91 (m, 1H), vol.5

, Association Business, Journal of Geoscience Education, vol.47, issue.5, pp.472-472, 1999.

D. D. Davey, ChemInform Abstract: Synthesis of 6-Phenylimidazo(1,2-a)pyrazin-8-one and 1-Methyl-6-phenylimidazo(1,5-a)pyrazin-8-one via Quaternary Intermediates., ChemInform, vol.19, issue.12, pp.1-31776, 1988.

H. Nmr, LOCAL GOVERNMENT DEPARTMENT., The Lancet, vol.126, issue.3229, pp.128-129, 1885.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, issue.6, p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid (0.24 g, 68%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.85 (s, 1H), 7.79 (m, 2H), 7.74 (m, 1H), 7.52 -7.33 (m, 10H), 7.28 (m, 1H), vol.8, pp.1-33067

H. Xu, A village in South Anhui, Management and Organization Review, vol.16, issue.3, pp.502-502, 2020.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a white solid (0.12 g, 34%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.96 (s (br), 1H), 7.89 (m, 2H), 7.82 (s, 1H), 7.79 (m, 1H), 7.52 -7.23 (m, 10H), vol.9, pp.1-33067

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.4, issue.6, p.5493, 1965.

, Chronicles, Soil Mechanics and Foundation Engineering, vol.3, issue.6, pp.448-448, 1966.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.14, p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.40 g, 95%) after dispertion of the reaction media in water, a filtration and drying under vacuum at 40°C. 1 H NMR (CDCl3): 7.84 (s, 1H), 7.75 (m, 2H), 7.34 (m, 9H), 6.97 (m, 2H), vol.21, pp.1-33069

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.26 g, 69%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.88 (s, 1H), 7.75 (m, 2H), 7.35 (m, 5H), 6.96 (m, 2H), vol.21, p.6

, Announcement, Psychophysiology, vol.29, issue.4, pp.460-460, 1992.

V. D. Dyachenko, Unexpected formation of 6-methyl-4-(5-methylfuran-2-yl)-2-ethylsulfanylpyridine-3-carbonitrile from 2-methyl-4-(5-methylfuran-2-yl)-N-o-tolyl-5-cyano-6-ethylsulfanyl-1,4-dihydropyridine-3-carboxamide, Russian Journal of Organic Chemistry, vol.47, issue.11, pp.1781-1782, 2011.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 88 (s, 1H), 7.75 (m, 2H), 7.34 (m, 4H), 6.96 (m, 2H), 6.05 (d, 1H, J = 3.0 Hz), 5.92

X. Wei, J. Miao, and L. Shi, Crystal structure of 2-(2-methyl-5-(6-(1-methyl-5-(pyrazin-2-yl)-1H-1,2,4- triazol-3-yl)pyridin-2-yl)-2H-1,2,4-triazol-3-yl)pyrazine manganese(II) dibromide, C19H15Br2MnN11, Zeitschrift für Kristallographie - New Crystal Structures, vol.230, issue.2, pp.123-124, 2015.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 88 (s, 1H), 7.75 (m, 2H), 7.33 (m, 4H), 6.97 (m, 2H), 6.06 (d, 1H, J = 3.0 Hz), vol.5

. Hz,

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.23 g, 75%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.88 (s, 1H), 7.75 (m, 2H), 7.34 (m, 4H), 6.96 (m, 2H), 5.95 (s, 1H), vol.21, pp.48-32712

, High Resolution 1H Detected Correlation Spectra in MAS Solid-State NMR: Perdeuterated Proteins with Selective 1H/2H Isotopic Labeling of Methyl Groups, H NMR (CDCl3): 7.90 (m, 2H), 7.87 (s, 1H), 7.48 (m, 2H), 7.43 (m, 1H), vol.22, pp.32712-32719

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 7.14 (m, 2H), 6.68 (tt, 1H, J = 9.1, 2.4 Hz), 6.36 (dd, 1H, J = 3.2, 1.9 Hz), 6.17 (m, 1H), vol.38

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.6, p.5493, 1965.

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 5.92 (m, 1H), 4.59 (s, 2H), 4.18 (s, 2H), vol.2

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.6, p.5493, 1965.

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., vol.38

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.22, issue.2, p.5493, 1965.

S. Ganesh, N. Saha, R. Zuckermann, and P. Sáha, Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate, Molbank, vol.2017, issue.1, p.M925, 2017.

H. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., CDCl3): 7.89 (s, 1H), 7.85 (m, 2H), 7.41 (m, 4H), 7.20 (ddd, 1H, J = 8.9, 5.7, 3.2 Hz), 7.05 (td, 1H, J = 8.9, 4.5 Hz), 6.93 (m, 1H), vol.6

J. Elguero and E. A. Et-al., ChemInform Abstract: Structure of NH-Benzazoles (1H-Benzimidazoles, 1H- and 2H-Indazoles, 1H- and 2H-Benzotriazoles), ChemInform, vol.44, issue.35, pp.no-no, 2013.

. Hz, 6.93 (m, 1H), 6.04 (d, 1H, J = 3.1 Hz), 5.92 (m, 1H)

C. Nmr, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., vol.157

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.08 g, 57%) after a chromatography over silica gel (cyclohexane -ethyl acetate 5/1). 1 H NMR (CDCl3): 7.89 (s, 1H), 7.85 (m, 2H), 7.43 (m, 3H), vol.7

, ????? ?????? ?????, pp.488-1786, 1786.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.17 g, 71%) after a chromatography over silica gel (cyclohexane -ethyl acetate 5/1). 1 H NMR (CDCl3): 7.89 (s, 1H), 7.85 (m, 2H), 7.42 (m, 3H), 7.21 (m, 1H), 7.05 (m, 1H), 6.93 (m, 1H), vol.5, p.12

. Hz, 126.6, 126.5 (m), 126.2, 123.5 (4 and 6 Hz), vol.115

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a solid (0.24 g, 73%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 7.88 (s, 1H), 7.85 (m, 2H), 7.41 (m, 4H), 7.22 (tt, 1H, J = 6.1, 1.7 Hz), 7.05 (m, 2H), 6.36 (dd, 1H, J = 3.2, 1.9 Hz), 6.18 (m, 1H), vol.24, pp.32712-32733

R. Siegmann and S. Beuermann, Individual Rate Coefficients for 1H,1H,2H,2H-Tridecafluorooctyl Methacrylate Radical Polymerizations, Macromolecules, vol.43, issue.8, pp.3699-3704, 2010.

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., vol.2

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 88 (s, 1H), 7.85 (m, 2H), 7.44 (m, 2H), 7.39 (m, 1H), 7.23 (m, 1H), 7.05 (m, 2H), 6.05 (d, 1H, J = 3.0 Hz), 5.93 (d, 1H, J = 3.0 Hz), 4.72 (s, 2H), 4.20 (s, 2H), 2.63 (q, 2H, J = 7.5 Hz), vol.2

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., H NMR (CDCl3): 7.88 (s, 1H), 7.84 (m, 2H), 7.46-7.35 (m, 3H), 7.21 (m, 1H), 7.11 -6.99 (m, 2H), 5.97 (s, 1H), 4.72 (s, 2H), 4.18 (s, 2H), 2.56 (m, 2H), 2.40 (m, 2H), 2.39 (s, 3H), 1.83 (m, 2H), 1.72 (m, 2H). 13 C NMR (CDCl3): 167.1, 150.9, vol.24, pp.49-33068

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.4, issue.2, p.5493, 1965.

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., 148.2, 149.5 (13 and 248 Hz, vol.126

. Hz, Figure 2. Point of subjective equality (PSE) obtained using two interval forced choice paradigm.

, Books Received, Radiology, vol.38, issue.4, pp.502-502, 1942.

, 23?-Isopropyl-24-methylcycloart-25-en-3?-yl Acetate, Natural Compounds, vol.24, pp.186-186, 2013.

H. Nmr, CDCl3): 7.88 (s, 1H), 7.85 (m, 2H), 7.43 (m, 2H), 7.38 (m, 1H), 7.22 (m, 1H), vol.7

C. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 85 (s, 1H), 7.84 (m, 2H), 7.43 -7.26 (m, 9H), 7.02 (m, 1H), 6.84 (m, 1H), 4.70 (s, 2H), 4.21 (s, 2H), 2.22 (s, 3H). 13 C NMR (CDCl3): 167.0, 157.1 (242, 12 and 3 Hz), vol.115

, Melanin-Concentrating Hormone Receptor 1 Antagonists Lacking an Aliphatic Amine: Synthesis and StructureActivity Relationships of Novel 1(Imidazo[1,2a]pyridin-6-yl)pyridin-2(1H)one Derivatives, vol.35, pp.30367-30412

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 8.50 (dd, 1H, J = 1.7, 5.0 Hz), 7.92 (m, 1H), 7.87 (m, 2H), 7.82 (s, 1H), 7.48-7.22 (m, 9H)

H. Nmr, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 2H dt, J = 3.0, 1.8 Hz), 7.78 (s, 1H), 7.48 -7.41 (m, 2H), 7.40 -7.35 (m, 1H), vol.7, pp.34-41

. Hz, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., vol.124

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 8.06 (s, 1H), 7.60 (m, 2H), 7.38-7.21 (m, 7H), 7.15 (m, 1H), 7.01 (m, 2H)

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, issue.6, p.5493, 1965.

C. Nmr, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., J = 23 Hz), vol.112, issue.9

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a glass (0.08 g, 72%). 1 H NMR (CDCl3): 8.19 (dt, 1H, J = 1.8, 7.8 Hz), 8.09 (s, 1H), 7.61 (m, 2H), 7.37-7.21 (m, 5H), vol.7, pp.30531-169

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters., vol.115

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a wax (0.18 g, 95%). 1 H NMR (CDCl3): 8.19 (dt, 1H, J = 1.8, 7.8 Hz), 8.10 (s, 1H), 7.62 (m, 2H), 7.39-7.22 (m, 5H), vol.7, pp.30367-111

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a wax (0.44 g, 95%). 1 H NMR (CDCl3): 8.20 (dt, 1H, J = 1.8, 8.0 Hz), 8.09 (s, 1H), 7.61 (m, 2H), 7.37 -7.24 (m, 5H), 7.15 (ddd, vol.25, pp.48-30367

. Hz, Two-Frame Marker for 48(/1.001)-Hz, 50-Hz, and 60(/1.001)-Hz Progressive Digital Video Signals on 1.5 Gb/s and 3 Gb/s Interfaces, vol.124, p.22

. Hz, Figure 1?source data 1. Intracellular voltage responses of the same R1-R6 photoreceptor to very bright 20 Hz, 50 Hz, 100 Hz, 200 Hz and 500 Hz bursty light stimuli at BG0 (darkness)., vol.112

J. M. Murray, CREBBP bromodomain in complex with Cpd 30 (1-(3-(3-(1-methyl-1H-pyrazol-4-yl)isoquinolin-8-yl)-1-(tetrahydro-2H-pyran-4-yl)-1,4,6,7-tetrahydro-5H-pyrazolo[4,3-c]pyridin-5-yl)ethan-1-one), H NMR (CDCl3): 8.17 (m, 2H), 7.32 (m, 5H), vol.1, 2018.

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 6.94 (m, 1H), 6.03 (d, 1H, J = 2.8 Hz), 5.92 (m, 1H), vol.160

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a glass (0.1 g, 83%). 1 H NMR (CDCl3): 7.88 (m, 2H), 7.78 (s, 1H), 7.59 (m, 2H), 7.34-7.12 (m, 6H), vol.6, pp.30531-171

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.25, issue.6, p.5493, 1965.

J. Grafius, Reviews, Heredity, vol.15, issue.4, pp.452-452, 1960.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as a beige solid (0.27 g, 68%) after a recrystallization from n-heptane. 1 H NMR (CDCl3): 8.21 (s, 1H), 8.05 (dd, 1H, J = 7.7, 1.8 Hz), 7.59 (dd, 2H, J = 7.9, 0.9 Hz), 7.39 -7.27 (m, 4H), 7.23 -7.18 (m, 1H), 7.09 (td, 1H, J = 7.6, 1.1 Hz), vol.6

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

C. Nmr, HRMS (m/z): [M+H] + calcd for C29H26N3O4, 468.1923; found, 468.1919. 2,8-Dibenzyl-6-(2,6-difluorophenyl)imidazo[1,2-a]pyrazin-3-yl acetate 25{10,1,1} (MM34284-035-1): Obtained as a solid (0.16 g, 61%) after a recrystallization from n-heptane, 84 (m, 2H), 7.75 (s, 1H), 7.61 (m, 2H), 7.32 (m, 2H), 7.24 (m, 1H), 7.0 (m, 2H), 6.02 (m, 1H), 5.91 (m, 1H), 4.62 (s, 2H), 4.17 (s, 2H), vol.3

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

. Hz, Figure 5. Electrical synapses between Shox2 INs act as low-pass filters.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, issue.6, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.5, p.5493, 1965.

, Effect of Sodium Sulfate, Ammonium Chloride, Ammonium Nitrate, and Salt Mixtures on Aqueous Phase Partitioning of Organic Compounds, vol.23

, Chemical structure 18. (Z)-4-((3-((benzyloxy)carbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)amino)-4-oxobut-2-enoic acid (13m), vol.1, pp.18-31777

H. Nmr, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., DMSO-d6, very badly resolved, containing AcOEt): 8.32 (s (br), 1H), 7.79 (m, 2H), 7.43 -6.93 (m, 14H), 6.84 (s(br), 1H), 6.72 (m, 2H), 6.56 (s(br), 1H)

H. Nmr, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., DMSO-d6, very badly resolved, containing AcOEt): 8.34 (s (br), 1H), 7.81 (m, 2H), 7.41 -7.10 (m, 13H), 6.99 (m, 2H), 6.69 (m, 2H), 6.47 (s(br), 1H), 4.91 (s, 2H), 4.60 (s(br), 1H), 4.13 (s(br), 1H), 3.92 (m, 1H), 3.23 (m, 1H), 3.10 (m, 1H). 13 C NMR

, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., -(Benzyloxy)benzyl)-5-phenylpyrazin-2-yl)phenylalanine 24{1,17,1} (YJ31776-155-1): 1 H NMR (DMSO-d6, very badly resolved, containing AcOEt): 8.38 (s (br), 1H), 7.86 (m, 2H), 7.41 -7.25 (m, 8H), 7.12 -6.97 (m, 6H), 6.93 (s(br), 1H), 6.82 (m, 2H), 6.48 (s(br), 1H), 5.07 (m, 2H)

I. E. Dolgii, G. P. Okonnishnikova, and O. M. Nefedov, ChemInform Abstract: 1H,2H- and 1H-Cyclopropene-3,3-dicarboxylates and 1H,2H-Cyclopropene3,3-dicarboxylic Acid from the Corresponding Trimethylsilyl Derivatives., ChemInform, vol.18, issue.28, 1987.

C. Nmr, ARCHAEOLOGY IN WEST CORNWALL, Antiquity, vol.33, issue.130, pp.127-128, 1959.

, Solid-Supported Acids for Debenzylation of Aryl Benzyl Ethers

, Figure 10: Double reciprocal plot of 1/[S] (L/mmol) and 1/v (104 Ls/mmol).

, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., -Benzyl-5-phenylpyrazin-2-yl)amino)-3-(3-hydroxyphenyl)propanoic acid 24{1,1,62} (YJ31777-045-1): 1 H NMR (DMSO-d6, containing EtOH): 8.45 (s, 1H), 8.40 (s, 1H), 7.89 (m, 2H), 7.40 (m, 2H), 7.30 -7.14 (m, 6H), 6.91 (m, 1H), 6.67 (m, 1H), 6.52 (m, 3H), 4.46 (s (br), 1H)

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.61, issue.3, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.18, p.5493, 1965.

E. N. Sokolov, Sensation seeking and the orienting reflex, Behavioral and Brain Sciences, vol.7, issue.3, pp.450-450, 1984.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.63, issue.6, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.8, issue.6, p.5493, 1965.

W. J. Feast and R. Stephens, 1022. Fluorocyclohexanes. Part XI. 1H,3H/2H-, 1H,2H/3H-, and 1H,2H,3H/-nonafluorocyclohexane, Journal of the Chemical Society (Resumed), vol.1, issue.2-, p.5493, 1965.

C. , 19. Besonderheiten, Wählerzahlberechnung, pp.129-133, 1939.

, Synthesis of b-Amino-a-hydroxy Esters and b-Amino-a-azido Ester by Sharpless Asymmetric Aminohydroxylation, Byproducts Analysis

F. Mol and . Base, Supplementary file 2. Oligonucleotides used in this study, RNA-seq and ATLAS-seq statistics.

J. M. Murray and C. Noland, CREBBP bromodomain in complex with Cpd59 ((S)-1-(3-((2-fluoro-4-(1-methyl-1H-pyrazol-4-yl)phenyl)amino)-1-(tetrahydrofuran-3-yl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridin-5(4H)-yl)ethanone), 2016.

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 93%). 1 H NMR (CDCl3): mixture of isomer: 7.23 (s, 1H), 5.63 (s, 1H), 4.02 (m, 2H), 3.88 (m, 1H), 3.74 (m, 1H), 3.56 (m, 1H), 2.07 (m, 1H), 1.89 (m, 5H), 1.54 (m, 1H). 13 C NMR

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an orange solid (3.46 g, 99%). 1 H NMR (DMSO-d6): 8.42 (m, 1H), 8.40 (dd, 1H, J = 1.9, 4.6 Hz), 7.62 (m, 1H), 7.26 (m, 2H), 6.95 (s (br), 1H)

, Chemicals used for treatment of swimming pool water. Sodium hydroxide

R. Ranjbar-karimi, T. Davodian, and H. Mehrabi, Reactions of pyridin-2-ol, pyridin-3-ol, and pyridin-4-ol with pentafluoro- and pentachloropyridine, Chemistry of Heterocyclic Compounds, vol.53, issue.12, pp.1330-1334, 2017.

H. Nmr, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., DMSO-d6): 12.47 (s(br), 1H), 8.57 (d, 1H, J = 1.7 Hz), 8.43 (dd, 1H, J = 1.7, 4.8 Hz), 7.89 (s, 1H), 7.92 (m, 2H), 7.74 (m, 1H)

, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., 45%) which was used without any further purification in the step viii described above. 1 H NMR (CDCl3): 13.22 (s(br), 1H), 7.81 (m, 2H), 7.63 (s (br), 1H), 7.44 (m, 2H), 7.35 (m, 1H), 4.60 (p, 1H, J = 6.6 Hz), 3.99 (m, 1H), 3.80 (m, 1H)

, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., vol.60, pp.30612-133

C. Nmr, Highly Viscous Binary Solvents: DMSO-d6/Glycerol and DMSO-d6/Glycerol-d8 for Polar and Apolar Mixture Analysis by NMR

B. Dietrich, Coupling of Boc-phenylalanine with phenylalanine ethyl ester hydrochloride, GG 30532-125-1) 1 H NMR (CDCl3): 7.38-7.28 (m, 7H), 2020.

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., (m, 2H), 1.73 (s, 1H), 1.03-0.98 (m, 3H). 13 C NMR (CDCl3): 172.0, 139.5, 138.0, 129.3, 128.9

. Hz, Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1.

. Hz, 13 C NMR (CDCl3): 159.9

, Figure 3?figure supplement 7. 1H and 13C NMR spectra of compound 2., s, 1H), 7.48 (m, 2H), 7.41 (m, 2H), 7.34-7.25 (m, 5H)

, Preparation of a Nitrogen Oil Compound Fraction by Modified Gel Silica Column Chromatography

H. Nmr, CDCl3): 7.61 (m, 2H), 7.50 (m, 3H), 7.39 (m, 2H), 7.32 (m, 2H), 7.25 (m, 1H)

C. Nmr-;-q, 1. , and J. =. , Figure 4?figure supplement 1. NMR spectrometry of synthesized G-1., Obtained as an oil (0.4 g, 84%) using the N-arylation protocol (step x) described above for the preparation of compounds 23, after a chromatography over silica gel (cyclohexane -ethyl acetate 94/6). 1 H NMR (CDCl3): 7.60-7.57 (m, 2H), 7.48-7.44 (m, 2H), 7.39-7.35 (m, 1H), 7.31-7.20 (m, 8H), 7.03-7.00 (m, 2H), vol.1

, This was cooled to -78 °C, and a 2M solution of lithium diisopropylamide (2 mL, 4.02 mmol, in THF, n-heptane and ethylbenzene) was injected. This was stirred at -78 °C for 10 minutes (immediate blackening of the solution) and methyl iodide (0.27 mL, 4.35 mmol) was then injected. This was stirred for 10 minutes at -78 °C and allowed to warm back to room temperature for 20 minutes. The resulting solution was diluted in water and ethyl acetate, the organic layer was washed with water, brine, dried over magnesium sulfate and concentrated to dryness. The residue was purified by a chromatography over silica gel (cyclohexane -dichloromethane 3/1) to yield compound 33 as a solid (0.73 g, 73%), This compound was obtained using the cyclization/O-acetylation protocol described above (step xii) as a white powder after a recrystallization from n-heptane (0.12 g, 44%). 1 H NMR (CDCl3): 7.90 (m, 2H), 7.74 (s, 1H), 7.68 (m, 2H), 7.46 (m, 2H), 7.40 (m, 1H), 7.33 (m, 5H), 7.25 (m, 2H), 4.68 (d, 1H, J = 13.8 Hz), 4.63 (d, 1H, J = 13.8 Hz), 4.34 (q, 1H, J = 6.7 Hz), 2.14 (s, 3H), 1.83 (d, 3H, J = 6.7 Hz). 13 C NMR (CDCl3): 167.1, 153.0, 143.9, vol.8, pp.31067-31090

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, A 26dB-Gain 100GHz Si/SiGe Cascaded Constructive-Wave Amplifier

, New Products, Physics Today, vol.42, issue.9, pp.105-107, 1989.

, New Products, IEEE Communications Magazine, vol.42, issue.11, pp.24-25, 2004.

, Products & Information, Rehabilitation Nursing, vol.25, issue.3, pp.113-113, 2000.

, Methods of test for starch hydrolysis products

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, From Reaction Order to the Michaelis-Menten Law: Fundamental Relationships of Enzyme Kinetics, Enzyme Kinetics, pp.55-86, 2017.

. Finally, as another illustration of this enzyme death over time, we provide in the following the signal profile over time for compound 5 and for the flashy compound 26bf

A. Szabo, Information processing time decreases as exercise intensity increases but the (expected) affective benefits are absent, 2003.

H. Chen, X. Han, N. Qin, L. Wei, Y. Yang et al., Synthesis and biological evaluation of novel inhibitors against 1,3,8-trihydroxynaphthalene reductase from Magnaporthe grisea, Bioorganic & Medicinal Chemistry, vol.24, issue.6, pp.1225-1230, 2016.

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E. P. Coutant, S. Goyard, V. Hervin, G. Gagnot, R. Baatallah et al., Gram-scale synthesis of luciferins derived from coelenterazine and original insights into their bioluminescence properties, Organic & Biomolecular Chemistry, vol.17, issue.15, pp.3709-3713, 2019.
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