Название: Catalytic Asymmetric Synthesis
Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Жанр: Химия
isbn: 9781119736417
isbn:
66 66. Barrio, P.; Rodríguez, E.; Saito, K.; Fustero, S.; Akiyama, T. Chem. Commun. 2015, 51, 5246–5249.
67 67. Gao, S.; Duan, M.; Houk, K.; Chen, M. Angew. Chem. Int. Ed. 2020, 59, 10540–10548.
68 68. (a) Wang, M.; Khan, S.; Miliordos, E.; Chen, M. Adv. Synth. Catal. 2019, 360, 4634–4639. (b) Liu, J.; Chen, M. Org. Lett. 2020, 22, 8967–8972.
69 69. Miura, T.; Nakahashi, J.; Murakami, M. Angew. Chem. Int. Ed. 2017, 56, 6989–6993.
70 70. Miura, T.; Nakahashi, J.; Zhou, W.; Shiratori, Y.; Stewart, S. G.; Murakami, M. J. Am. Chem. Soc. 2017, 139, 10903–10908.
71 71. Mahlau, M.; García‐García, P.; List, B. Chem. Eur. J. 2012, 18, 16283–16287.
72 72. Kaib, P. S. J.; Schreyer, L.; Lee, S.; Properzi, R.; List, B. Angew. Chem. Int. Ed. 2016, 55, 13200–13203.
73 73. Bae, H. Y.; Höfler, D.; Kaib, P. S. J.; Kasaplar, P.; De, C. K.; Döhring, A.; Lee, S.; Kaupmees, K.; Leito, I.; List, B. Nat. Chem. 2018, 10, 888–894.
74 74. Lee, D. S.; Bae, H. Y.; List, B. Angew. Chem. Int. Ed. 2018, 57, 12162–12166.
75 75. Min, D. C.; Lin, Y.; Seidel, D. Angew. Chem. Int. Ed. 2017, 56, 15353–15357.
76 76. Rajkumar, S.; Tang, M.; Yang, X. Angew. Chem. Int. Ed. 2020, 59, 2333–2337
77 77. Das, S.; Liu, L.; Zheng, Y.; Alachraf, M. W.; Thiel, W.; De, C. K.; List, B. J. Am. Chem. Soc. 2016, 138, 9429–9432.
78 78. Maskeri, M. A.; O'Connor, M. J.; Jaworski, A. A.; Davies, A. V.; Scheidt, K. A. Angew. Chem. Int. Ed. 2018, 57, 17225–17229.
79 79. Zhao, C.; Chen, S. B.; Seidel, D. J. Am. Chem. Soc. 2016, 138, 9053–9056.
80 80. Zhu, Z.; Odagi, M.; Zhao, C.; Abboud, K. A.; Kirm, H. U.; Saame, J.; Lõkov, M.; Leito, I.; Seidel, D. Angew. Chem. Int. Ed. 2020, 59, 2028–2032.
81 81. For a review on enantioselective cycloaddition reaction catalyzed by chiral phosphoric acids, see: Held, F. E.; Grau, D.; Tsogoeva, S. B. Molecules 2015, 20, 16103–16126.
82 82. Gatzenmeier, T.; van Gemmeren, M.; Xie, Y.; Höfler, D.; Leutzsch, M.; List, B. Science 2016, 351, 949–952.
83 83. Gatzenmeier, T.; Turberg, M.; Yepes, D.; Xie, Y.; Neese, F.; Bistoni, G.; List, B. J. Am. Chem. Soc. 2018, 140, 12671–12676.
84 84. Kim, H.; Gerosa, G.; Aronow, J.; Kasaplar, P.; Ouyang, J.; Lingnau, J. B.; Guerry, P.; Farès, C.; List, B. Nat. Commun. 2019, 10 770.
85 85. Ghosh, S.; Das, S.; De, C. K.; Yepes, D.; Neese, F.; Bistoni, G.; Leutzsch, M.; List, B. Angew. Chem. Int. Ed. 2020, 59, 12347–12351.
86 86. Varlet, T.; Gelis, C.; Retailleau, P.; Bernadat, G.; Neuville, L.; Masson, G. Angew. Chem. Int. Ed. 2020, 59, 8491–8496.
87 87. Hatano, M.; Goto, Y.; Izumiseki, A.; Akakura, M.; Ishihara, K. J. Am. Chem. Soc. 2015, 137, 13472–13475.
88 88. Akiyama, T.; Morita, H.; Fuchibe, K. J. Am Chem. Soc. 2006, 128, 13070–13071.
89 89. (a) Liu, H.; Dagousset, G.; Masson, G.; Retailleau, P.; Zhu, J. J. Am. Chem. Soc. 2009, 131, 4598–4599. (b) Dagousset, G.; Zhu, J.; Masson, G. J. Am. Chem. Soc. 2011, 133, 14804–14813.
90 90. For a review, see: Varleta, T.; Masson, G. Chem. Commun. 2021, 57, 4089–4105.
91 91. Jarrige, L.; Blanchard, F.; Masson, G. Angew. Chem. Int. Ed. 2017, 56, 10573–10576.
92 92. (a) Luo, C.; Huang, Y. J. Am. Chem. Soc. 2013, 135, 8193–8196. (b) See also: Dai, W.; Jiang, X.‐L.; Tao, J.‐Y.; Shi, F. J. Org. Chem. 2016, 81, 185–192.
93 93. Momiyama, N.; Tabuse, H.; Noda, H.; Yamanaka, M.; Fujinami, T.; Yamanishi, K.; Izumiseki, A.; Funayama, K.; Egawa, F.; Okada, S.; Adachi, H.; Terada, M. J. Am. Chem. Soc. 2016, 138, 11353–11359.
94 94. Kretzschmar, M.; Hodík, T.; Schneider, C. Angew. Chem. Int. Ed. 2016, 55, 9788–9792.
95 95. Hatano, M.; Nishikawa, K.; Ishihara, K. J. Am. Chem. Soc. 2017, 139, 8424–8427.
96 96. Nakanishi, T.; Kikuchi, J.; Kaga, A.; Chiba, S.; Terada, M. Chem. Eur. J. 2020, 26, 8230–8234.
97 97. Zhao, J.‐J.; Sun, S.‐B.; He, S.‐H.; Wu, Q.; Shi, F. Angew. Chem. Int. Ed. 2015, 54, 5460–5464.
98 98. El‐Sepelgy, M. S. O.; Haseloff, M. S. S.; Alamsetti, S. K.; Schneider, C. Angew. Chem. Int. Ed. 2014, 53, 7923–7927.
99 99. Alamsetti, S. K.; Spanka, M.; Schneider, C. Angew. Chem. Int. Ed. 2016, 55, 2392–2396.
100 100. Wang, Y.‐M.; Zhang, H.‐H.; Li, C.; Fan, T.; Shi, F. Chem. Commun. 2016, 52, 1804–1807.
101 101. Tan, W.; Li, X.; Gong, Y.‐X.; Ge, M.‐D.; Shi, F. Chem. Commun. 2014, 50, 15901–15904.
102 102. For a review on enantioselective reactions of indolylmethanol catalyzed by chiral phosphoric acid, see: Mei, G.‐J.; Shi, F. J. Org. Chem 2017, 82, 7695–7707.
103 103. For a review on enantioselective reactions of indole‐based chiral heterocycles catalyzed by chiral phosphoric acid, see: Zhang, Y.‐C.; Jiang, F.; Shi, F. Acc. Chem. Res. 2020, 53, 425–446.
104 104. Gelis, C.; Levitr, G.; Merad, J.; Retailleau, P.; Neuville, L.; Masson, G. Angew. Chem. Int. Ed. 2018, 57, 12121–12125.
105 105. Bera, K.; Schneider, C. Chem. Eur. J. 2016, 22, 7074–7078.
106 106. Zhu, Z. Q.; Shen, Y.; Sun, X. X.; Tao, J. Y.; Liu, J. X.; Shi, F. Adv. Synth. Catal. 2016, 358, 3797–3808.
107 107. Sun, X. X.; Zhang, H. H.; Li, G. H.; He, Y. Y.; Shi, F. Chem. Eur. J. 2016, 22, 17526–17532.
108 108. Suneja, A.; Loui, H. J.; Schneider, C. Angew. Chem. Int. Ed. 2020, 59, 5536–5540.
109 109. Villar, L.; Uria, U.; Martínez, J. I.; Prieto, L.; Reyes, E.; Carrillo, L.; Vicario, J. L. Angew. Chem. Int. Ed. 2017, 56, 10535–10538.
110 110. Rueping, M.; Ieawsuwan, W.; Antonchick, A. P.; Nachtsheim, B. J. Angew. Chem. Int. Ed. 2007, 46, 2097–2100.
111 111. Jolit, A.; Walleser, P. M.; Yap, G. P. A.; Tius, M. A. Angew. Chem. Int. Ed. 2014, 53, 6180–6183.
112 112. Ouyang, J.; Kennemur, J. L.; De, C. K.; Farès, C.; List, B. J. Am. Chem. Soc. 2019, 141, 3414–3418.
113 113. Jin, J.; Zhao, Y.; Gouranourimi, A.; Ariafard, A.; Chan, P. W. H. J. Am. Chem. Soc. 2018, 140, 5834–5841.
114 114. Yang, B.‐M.; Cai, P.‐J.; Tu, Y.‐Q.; Yu, Z.‐X.; Chen, Z.‐M.; Wang, S.‐H.; Wang, S.‐H.; Zhang, F.‐M. J. Am. Chem. Soc. 2015, 137, 8344–8347.
115 115. Felker, I.; Pupo, G.; Kraft, P.; List, B. Angew. Chem. Int. Ed. 2015, 54, 1960–1964.
116 116. Wang, Y.‐Y.; Kanomata, K.; Korenaga, T.; Terada, M. Angew. Chem. Int. Ed. 2016, 55, 927–931.
117 117. Uraguchi, D.; Kinoshita, СКАЧАТЬ