Catalytic Asymmetric Synthesis. Группа авторов
Чтение книги онлайн.

Читать онлайн книгу Catalytic Asymmetric Synthesis - Группа авторов страница 54

Название: Catalytic Asymmetric Synthesis

Автор: Группа авторов

Издательство: John Wiley & Sons Limited

Жанр: Химия

Серия:

isbn: 9781119736417

isbn:

СКАЧАТЬ 29, 1181–1192. (k) Xia, Z.‐L.; Xu‐Xu, Q.‐F.; Zheng, C.; You, S.‐L. Chem. Soc. Rev. 2020, 49, 286–300.

      16 16. (a) Maruoka, K. ed. Asymmetric Organocatalysis 2, Brønsted base and acid catalysts, and additional topics. In: Science of Synthesis, Stuttgart, Germany, Georg Thieme Verlag KG, 2012. (b).Rueping, M., Parmar, D., and Sugiono, E. eds Asymmetric Brønsted Acid Catalysis, Weinheim, Germany: Wiley‐VCH. 2016.

      17 17. (a) Yang, C.; Xue, X.‐S.; Jin, J.‐L.; Li, X.; Cheng, J.‐P. J. Org. Chem. 2013, 48, 7076–7085. (b) Yang, C.; Xue, X.‐S.; Li, X.; Cheng, J.‐P. J. Org. Chem. 2014, 79, 4340–4351.

      18 18. Guo, Q.‐X.; Liu, H.; Guo, C.; Luo, S.‐W.; Gu, Y.; Gong, L.‐Z. J. Am. Chem. Soc. 2007, 129, 3790–3791.

      19 19. For a review on SPINOL derived chiral phosphoric acid, see: Rahman, A.; Lin, X. Org. Biomol. Chem. 2018, 16, 4753–4777.

      20 20. Coric, I.; Müller, S.; List, B. J. Am. Chem. Soc. 2010, 132, 17370–17373.

      21 21. Nakashima, D.; Yamamoto, H. J. Am. Chem. Soc. 2006, 128, 9626–9627.

      22 22. (a) Christ, P.; Lindsay, A. G.; Vormittag, S. S.; Neudörfl, J.‐M.; Berkessel, A.; O'Donoghue, A. C. Chem. Eur. J. 2011, 17, 8524–8528. (b) Kaupmees, K.; Tolstoluzhsky, N.; Raja, S.; Rueping, M.; Leito, I. Angew. Chem. Int. Ed. 2013, 52, 11569–11572.

      23 23. For a review on ACDC, see: Mahlau, M.; List, B. Angew. Chem. Int. Ed. 2013, 52, 518–533.

      24 24. (a) Phipps, R. J.; Hamilton, G. L.; Toste, F. D. Nature Chem. 2012, 4, 603–614. (b) See also, Brak, K.; Jacobsen, E. N. Angew. Chem. Int. Ed. 2013, 52, 534–561.

      25 25. Toste, D. (this issue), Chapter 4 – Asymmetric phase transfer and ion pair organocatalysis. In: Akiyama, T. and Ojima, I. Catalytic Asymmetric Synthesis, 4e, Wiley.

      26 26. Parra, A.; Reboredo, S.; Castro, A. M. M.; Alemán, J. Org. Biomol. Chem. 2012, 10, 5001–5020

      27 27. (a) For reviews, see: Zhong, C.; Shi, X. Eur. J. Org. Chem. 2010, 2010 2999–3025. (b) Piovesana, S.; Scarpino Schietroma, D. M.; Bella, M. Angew. Chem. Int. Ed. 2011, 50, 6216–6232. (c) Brière, J.‐F.; Oudeyer, S.; Dalla, V.; Levacher, V. Chem. Soc. Rev. 2012, 41, 1696–1707. (d) Tran, V. T.; Nimmagadda, S. K.; Liu, M.; Engle, K. M. Org. Biomol. Chem. 2020, 18, 618–637.

      28 28. (a) Inanaga, J.; Sugimoto, Y.; Hanamoto, T. New J. Chem. 1995, 19, 707–712. (b) Furuno, H.; Hanamoto, T.; Sugimoto, Y.; Inanaga, J. Org. Lett. 2000, 2, 49–52.

      29 29. Hatano, M.; Ikeno, T.; Matsumura, T.; Torii, S.; Ishihara, K. Adv. Synth. Catal. 2008, 350, 1776–1780.

      30 30. Drouet, F.; Lalli, C.; Liu, H.; Masson, G.; Zhu, J. Org. Lett. 2010, 13, 94–97.

      31 31. Ingle, G. K.; Liang, Y.; Mormino, M. G.; Li, G.; Fronczek, F. R.; Antilla, J. C. Org. Lett. 2011, 13, 2054–2057.

      32 32. (a) Hatano, M.; Moriyama, K.; Maki, T.; Ishihara, K. Angew. Chem. Int. Ed. 2010, 49, 3823–3826. (b) Hatanoa, M.; Ishihara, K. Synthesis 2010, 3785–3801

      33 33. Klussmann, M.; Ratjen, L.; Hoffmann, S.; Wakchaure, V.; Goddard, R.; List, B. Synlett 2010, 2189–2192.

      34 34. For an example, see: Prashad, M.; Hu, B.; Repi, O.; Blacklock, T. J.; Giannousis, P. Org. Process Res. Dev. 2000, 4, 55–59.

      35 35. Yamanaka, M.; Itoh, J.; Fuchibe, K.; Akiyama, T. J. Am. Chem. Soc. 2007, 129, 6756–6764.

      36 36. Zhou, F.; Yamamoto, H. Angew. Chem. Int. Ed. 2016, 55, 8970–8974

      37 37. Gheewala, C. D.; Collins, B. E.; Lambert, T. H. Science 2016, 351, 961–965

      38 38. Hatano, M.; Maki, T.; Moriyama, K.; Arinobe, M.; Ishihara, K. J. Am. Chem. Soc. 2008, 130, 16858–16860.

      39 39. Zhu, C.; Mandrelli, F.; Zhou, H.; Maji, R.; List, B. J. Am. Chem. Soc. 2021, 143, 3312–3317.

      40 40. Seayad, J.; Seayad, A. M.; List, B. J. Am. Chem. Soc. 2006, 128, 1086–1087.

      41 41. Wang, S.‐G.; Xia, Z.‐L.; Xu, R.‐Q.; Liu, X.‐J.; Zheng, C.; You, S.‐L. Angew. Chem. Int. Ed. 2017, 56, 7440–7443.

      42 42. (a) Zahrt, A. F.; Henle, J. J.; Rose, B. T.; Wang, Y.; Darrow, W. T.; Denmark, S. E. Science 2019, 363, eaau5631. (b) See also: Reid, J. P.; Sigman, M. S. Nature 2019, 571, 343–348.

      43 43. Wang, Y.; Wang, Q.; Zhu, J. Angew. Chem. Int. Ed. 2017, 56, 5612–5615.

      44 44. Fan, L.; Han, C.; Li, X.; Yao, J.; Wang, Z.; Yao, C.; Chen, W.; Wang, T.; Zhao, J. Angew. Chem. Int. Ed. 2018, 57, 2115–2119.

      45 45. Kang, Q.; Zhao, Z.‐A.; You, S.‐L. J. Am. Chem. Soc. 2007, 129, 1484–1485.

      46 46. Xu, F.; Huang, D.; Han, C.; Shen, W.; Lin, X.; Wang, Y. J. Org. Chem. 2010, 75, 8677–8680.

      47 47. (a) For reviews, see: Zeng, M.; You, S.‐L. Synlett 2010, 1289–1301. (b) Terrasson, V.; Marcia de Figueiredo, R.; Campagne, J. M. Eur. J. Org. Chem 2010, 2635–2655.

      48 48. Hatano, M.; Mochizuki, T.; Nishikawa, K.; Ishihara, K. ACS Catal. 2018, 8, 349–353.

      49 49. Hatano, M.; Okamoto, H.; Kawakami, T.; Toh, K.; Nakatsuji, H.; Sakakura, A.; Ishihara, K. Chem. Sci. 2018, 9, 6361–6367.

      50 50. For a review on combined acid catalysis for asymmetric synthesis, see: Yamamoto, H.; Futatsugi, K. Angew. Chem. Int. Ed. 2005, 44, 1924–1942.

      51 51. Miyagawa, M.; Yoshida, M.; Kiyota, Y.; Akiyama, T. Chem. Eur. J. 2019, 25, 5677–5681.

      52 52. For a review on organocatalytic enantioselective Friedel‐Crafts alkylation reactions of pyrroles, see: Gaviña, D.; Escolano, M.; Torres, J.; Alzuet‐Piña, G.; Sánchez‐Roselló, M.; del Pozo, C. Adv. Synth. Catal. 2021, 363, 3439–3470.

      53 53. Uchikura, T.; Suzuki, R.; Suda, Y.; Akiyama, T. ChemCatChem 2020, 12, 4784–4787.

      54 54. Yonesaki, R.; Kondo, Y.; Akkad, W.; Sawa, M.; Morisaki, K.; Morimoto, H.; Ohshima, T. Chem. Eur. J. 2018, 24, 15211–15214.

      55 55. (a) Mori, K.; Ehara, K.; Kurihara, K.; Akiyama, T. J. Am. Chem. Soc. 2011, 133, 6166–6169. (b) See also, Mori, K.; Isogai, R.; Kamei, Y.; Yamanaka, M.; Akiyama, T. J. Am. Chem. Soc. 2018, 140, 6203–6207.

      56 56. Lee, S.; Kim, S. Tetrahedron 2009, 50, 3345–3348.

      57 57. Prévost, S.; Dupré, N.; Leutzsch, M.; Wang, Q.; Wakchaure, V.; List, B. Angew. Chem. Int. Ed. 2014, 53, 8770–8773.

      58 58. Liu, L.; Kaib, P. S. J.; Tap, A.; List, B. J. Am. Chem. Soc. 2016, 138, 10822–10825.

      59 59. Liu, L.; Leutzsch, M.; Zheng, Y.; Alachraf, M. W.; Thiel, W.; List, B. J. Am. Chem. Soc. 2015, 137, 13268–13271.

      60 60. Rueping, M.; Theissmann, T.; Kuenkel, A.; Koenigs, R. M. Angew. Chem. Int. Ed. 2008, 47, 6798–6801.

      61 61. Kikuchi, J.; Aramaki, H.; Okamoto, H.; Terada, M. Chem. Sci. 2019, 10, 1426–1433.

      62 62. Jain, P.; Antilla, J. C. J. Am. Chem. Soc. 2010, 132, 11884–11886.

      63 63. Jain, P.; Wang, H.; Houk, K. N.; Antilla, J. C. Angew. Chem. Int. Ed. 2012, 51, 1391–1394.

      64 64. СКАЧАТЬ