Читать книгу Methodologies in Amine Synthesis - Группа авторов - Страница 17

1 1 (a) Canè, F., Brancaleoni, D., Dembech, P. et al. New developments on organocopper‐mediated electrophilic amination. In: New Horizons in Organic Synthesis, 118–129. New Age International Publishers.(b) Bernardi, P., Dembech, P., Ricci, A., and Seconi, G. (1999). The Journal of Organic Chemistry 64: 641–643, and references therein.(c) Corpet, M. and Gosmini, C. (2014). Synthesis‐Stuttgart 46: 2258–2271.

2 2 Erdik, E. and Ay, M. (1989). Chemical Reviews 89: 1947–1980.

3 3 Dong, X., Liu, Q., Dong, Y., and Liu, H. (2017). Chemistry (Easton). 23: 2481–2511.

4 4 Zhou, Z. and Kürti, L. (2019). Synlett 30: 1525–1535.

5 5 Tsutsui, H., Ichikawa, T., and Narasaka, K. (1999). Bulletin of the Chemical Society of Japan 72: 1869–1878.

6 6 Tsutsui, H., Hayashi, Y., and Narasaka, K. (1997). Chemistry Letters 26: 317–318.

7 7 Erdik, E. and Daşkapan, T. (1999). Synthetic Communications 29: 3989–3997.

8 8 Erdik, E. and Daşkapan, T. (1999). Journal of the Chemical Society, Perkin Transactions 1 21: 3139–3142.

9 9 Berman, A.M. and Johnson, J.S. (2004). Journal of the American Chemical Society 126: 5680–5681.

10 10 Berman, A.M. and Johnson, J.S. (2006). The Journal of Organic Chemistry 71: 219–224.

11 11 Garcia‐Lopez, J.A., Cetin, M., and Greaney, M.F. (2015). Angewandte Chemie (International Ed. in English) 54: 2156–2159.

12 12 Zhou, S., Yang, Z., Chen, X. et al. (2015). The Journal of Organic Chemistry 80: 6323–6328.

13 13 Nguyen, M.H. and Smith, A.B. (2013). Organic Letters 15: 4872–4875.

14 14 Zhou, Z., Ma, Z., Behnke, N.E. et al. (2017). Journal of the American Chemical Society 139: 115–118.

15 15 Tezuka, N., Shimojo, K., Hirano, K. et al. (2016). Journal of the American Chemical Society 138: 9166–9171.

16 16 Matsuda, N., Hirano, K., Satoh, T., and Miura, M. (2012). Angewandte Chemie (International Ed. in English) 51: 3642–3645.

17 17 Miki, Y., Hirano, K., Satoh, T., and Miura, M. (2013). Organic Letters 15: 172–175.

18 18 Miura, T., Morimoto, M., and Murakami, M. (2012). Organic Letters 14: 5214–5217.

19 19 Matsuda, N., Hirano, K., Satoh, T., and Miura, M. (2012). Angewandte Chemie (International Ed. in English) 51: 11827–11831.

20 20 Matsuda, N., Hirano, K., Satoh, T., and Miura, M. (2013). Journal of the American Chemical Society 135: 4934–4937.

21 21 Miki, Y., Hirano, K., Satoh, T., and Miura, M. (2013). Angewandte Chemie (International Ed. in English) 52: 10830–10834.

22 22 Zhu, S., Niljianskul, N., and Buchwald, S.L. (2013). Journal of the American Chemical Society 135: 15746–15749.

23 23 Shi, S.L. and Buchwald, S.L. (2015). Nature Chemistry 7: 38–44.

24 24 Matsuda, N., Hirano, K., Satoh, T., and Miura, M. (2012). The Journal of Organic Chemistry 77: 617–625.

25 25 Shen, K. and Wang, Q. (2015). Chemical Science 6: 4279–4283.

26 26 Hemric, B.N., Shen, K., and Wang, Q. (2016). Journal of the American Chemical Society 138: 5813–5816.

27 27 Ye, Z. and Dai, M. (2015). Organic Letters 17: 2190–2193.

28 28 Matsuda, N., Hirano, K., Satoh, T., and Miura, M. (2011). Organic Letters 13: 2860–2863.

29 29 Yotphan, S., Beukeaw, D., and Reutrakul, V. (2013). Tetrahedron 69: 6627–6633.

30 30 Zhu, C., Yi, M., Wei, D. et al. (2014). Organic Letters 16: 1840–1843.

31 31 Johnson, J.S. and Berman, A.M. (2005). Synlett 11: 1799–1801.

32 32 Barker, T.J. and Jarvo, E.R. (2009). Journal of the American Chemical Society 131: 15598–15599.

33 33 Lutter, F.H., Graßl, S., Grokenberger, L. et al. (2019). ChemCat Chem 11: 5188–5197.

34 34 Yoo, E.J., Ma, S., Mei, T.S. et al. (2011). Journal of the American Chemical Society 133: 7652–7655.

35 35 He, J., Shigenari, T., and Yu, J.Q. (2015). Angewandte Chemie International Edition 54: 6545–6549.

36 36 Shang, M., Zeng, S.‐H., Sun, S.‐Z. et al. (2013). Organic Letters 15: 5286–5289.

37 37 Dong, Z. and Dong, G. (2013). Journal of the American Chemical Society 135: 18350–18353.

38 38 Huehls, C.B., Lin, A., and Yang, J. (2014). Organic Letters 16: 3620–3623.

39 39 Dequirez, G., Pons, V., and Dauban, P. (2012). Angewandte Chemie (International Ed. in English) 51: 7384–7395.

40 40 Shimbayashi, T., Sasakura, K., Eguchi, A. et al. (2019). Chemistry (Easton). 25: 3156–3180.

41 41 Starkov, P., Jamison, T.F., and Marek, I. (2015). Chemistry (Easton). 21: 5278–5300.

42 42 Kwart, H. and Khan, A.A. (1967). Journal of the American Chemical Society 89: 1951–1953.

43 43 Jat, J.L., Paudyal, M.P., Gao, H. et al. (2014). Science 343: 61–65.

44 44 Nicolaou, K.C., Rhoades, D., Wang, Y. et al. (2017). Journal of the American Chemical Society 139: 7318–7334.

45 45 Ma, Z., Zhou, Z., and Kürti, L. (2017). Angewandte Chemie, International Edition 56: 9886–9890.

46 46 Strom, A.E. and Hartwig, J.F.J. (2013). Organic Chemistry 78: 8909–8914.

47 47 Paudyal, M.P., Adebesin, A.M., Burt, S.R. et al. (2016). Science 353: 1144.

48 48 Zhu, C., Li, G., Ess, D.H. et al. (2012). Journal of the American Chemical Society 134: 18253–18256.

49 49 Gao, H., Zhou, Z., Kwon, D.‐H. et al. (2017). Nature Chemistry 9: 681–688.

50 50 Behnke, N.E., Kielawa, R., Kwon, D.‐H. et al. (2018). Organic Letters 20: 8064–8068.

51 51 Farndon, J.J., Young, T.A., and Bower, J.F. (2018). Journal of the American Chemical Society 140: 17846–17850.

52 52 Zhou, Z., Cheng, Q.‐Q., and Kürti, L. (2019). Journal of the American Chemical Society 141: 2242–2246.

53 53 Cheng, Q.‐Q., Zhou, Z., Jiang, H. et al. (2020). Nature Catalysis 3: 386–392.