Beilstein J. Org. Chem. 2020, 16, 492–501.
13.Williamson, A. E.; Ylioja, P. M.; Robertson, M. N.; Antonova-Koch, Y.;
Avery, V.; Baell, J. B.; Batchu, H.; Batra, S.; Burrows, J. N.;
Bhattacharyya, S.; Calderon, F.; Charman, S. A.; Clark, J.; Crespo, B.;
Dean, M.; Debbert, S. L.; Delves, M.; Dennis, A. S. M.; Deroose, F.;
Duffy, S.; Fletcher, S.; Giaever, G.; Hallyburton, I.; Gamo, F.-J.;
Gebbia, M.; Guy, R. K.; Hungerford, Z.; Kirk, K.;
vacuum and the desired product was purified by silica gel chro-
matography and a mixture of petroleum ether/ethyl acetate as
eluent.
Supporting Information
Lafuente-Monasterio, M. J.; Lee, A.; Meister, S.; Nislow, C.;
Overington, J. P.; Papadatos, G.; Patiny, L.; Pham, J.; Ralph, S. A.;
Ruecker, A.; Ryan, E.; Southan, C.; Srivastava, K.; Swain, C.;
Tarnowski, M. J.; Thomson, P.; Turner, P.; Wallace, I. M.;
Wells, T. N. C.; White, K.; White, L.; Willis, P.; Winzeler, E. A.;
Wittlin, S.; Todd, M. H. ACS Cent. Sci. 2016, 2, 687–701.
Supporting Information File 1
Characterization data and copies of NMR spectra.
14.Cai, L.; Qu, B.; Hurtle, B. T.; Dadiboyena, S.; Diaz-Arrastia, R.;
Pike, V. W. ACS Chem. Neurosci. 2016, 7, 897–911.
Funding
We acknowledge the Support of the National Natural Science
Foundation of China (No: 21702148), and the Foundation of
Department of Education of Guangdong Province (No:
2018KTSCX230, 2017KZDXM085, and 2018KZDXM070).
15.Przeslak, A. D.; Inman, M.; Lewis, W.; Moody, C. J. J. Org. Chem.
16.Singh, B.; Pennock, P. O.; Lesher, G. Y.; Bacon, E. R.; Page, D. F.
17.Mahy, W.; Plucinski, P.; Jover, J.; Frost, C. G. Angew. Chem., Int. Ed.
18.Ouyang, L.; Qi, C.; He, H.; Peng, Y.; Xiong, W.; Ren, Y.; Jiang, H.
19.Nocera, G.; Young, A.; Palumbo, F.; Emery, K. J.; Coulthard, G.;
McGuire, T.; Tuttle, T.; Murphy, J. A. J. Am. Chem. Soc. 2018, 140,
20.Barham, J. P.; Coulthard, G.; Emery, K. J.; Doni, E.; Cumine, F.;
Nocera, G.; John, M. P.; Berlouis, L. E. A.; McGuire, T.; Tuttle, T.;
Murphy, J. A. J. Am. Chem. Soc. 2016, 138, 7402–7410.
21.Rehan, M.; Maity, S.; Morya, L. K.; Pal, K.; Ghorai, P.
Angew. Chem., Int. Ed. 2016, 55, 7728–7732.
ORCID® iDs
Preprint
A non-peer-reviewed version of this article has been previously published
References
1. Arockiam, P. B.; Bruneau, C.; Dixneuf, P. H. Chem. Rev. 2012, 112,
2. Weng, Y.; Lv, W.; Yu, J.; Ge, B.; Cheng, G. Org. Lett. 2018, 20,
3. Luo, B.; Weng, Z. Chem. Commun. 2018, 54, 10750–10753.
22.Pichette Drapeau, M.; Fabre, I.; Grimaud, L.; Ciofini, I.; Ollevier, T.;
Taillefer, M. Angew. Chem., Int. Ed. 2015, 54, 10587–10591.
4. Johnson, J. S.; Evans, D. A. Acc. Chem. Res. 2000, 33, 325–335.
23.Feng, J.-B.; Wu, X.-F. Adv. Synth. Catal. 2016, 358, 2179–2185.
5. Gómez, M.; Muller, G.; Rocamora, M. Coord. Chem. Rev. 1999,
6. Gant, T. G.; Meyers, A. I. Tetrahedron 1994, 50, 2297–2360.
7. Magano, J. Chem. Rev. 2009, 109, 4398–4438.
8. de la Rosa, V. R.; Tempelaar, S.; Dubois, P.; Hoogenboom, R.;
Mespouille, L. Polym. Chem. 2016, 7, 1559–1568.
24.Wang, H.; Ying, J.; Lai, M.; Qi, X.; Peng, J.-B.; Wu, X.-F.
Adv. Synth. Catal. 2018, 360, 1693–1703.
25.Liu, S.; Zhang, S.; Lin, Q.; Huang, Y.; Li, B. Org. Lett. 2019, 21,
26.Midya, G. C.; Kapat, A.; Maiti, S.; Dash, J. J. Org. Chem. 2015, 80,
27.Hünig, S. Angew. Chem., Int. Ed. Engl. 1964, 3, 548–560.
9. Qiao, K.; Yuan, X.; Wan, L.; Zheng, M.-W.; Zhang, D.; Fan, B.-B.;
Di, Z.-C.; Fang, Z.; Guo, K. Green Chem. 2017, 19, 5789–5793.
28.Fenster, E.; Smith, B. T.; Gracias, V.; Milligan, G. L.; Aubé, J.
10.Gutmann, B.; Roduit, J.-P.; Roberge, D.; Kappe, C. O. Chem. – Eur. J.
11.Laitar, D. S.; Kramer, J. W.; Whiting, B. T.; Lobkovsky, E. B.;
Coates, G. W. Chem. Commun. 2009, 5704–5706.
12.Singh, S. P.; Parmar, S. S.; Raman, K.; Stenberg, V. I. Chem. Rev.
500