Название: Catalytic Asymmetric Synthesis
Автор: Группа авторов
Издательство: John Wiley & Sons Limited
Жанр: Химия
isbn: 9781119736417
isbn:
REFERENCES
1 1. (a) Palomo, C.; Oiarbide, M.; López, R. Chem. Soc. Rev. 2009, 38, 632–653. (b) Superbases for Organic Synthesis: Guanidines, Amidines, Phosphazenes and Related Organocatalysts; Ishikawa, T., Ed.; John Wiley & Sons: Chichester, West Sussex, 2009. (c) Comprehensive Enantioselective Organocatalysis; Dalko, P. I. Ed.; Wiley‐VCH: Weinheim, 2013, pp 343–363.
2 2. For pKBH+ values of organobases: (a) Tshepelevitsh, S.; Kütt, A.; LõKov, M.; Kaljurand, I.; Saame, J.; Heering, A.; Plieger, P. G.; Vianello, R.; Leito, I. Eur. J. Org. Chem. 2019, 6735–3748. (b) Schwesinger, R.; Schlemper, H.; Hasenfratz, C.; Willaredt, J.; Dambacher, T.; Breuer, T.; Ottaway, C.; Fletschinger, M.; Boele, J.; Fritz, H.; Putzas, D.; Rotter, H. W.; Boldwell, F. G.; Satish, A. V.; Ji, G.‐Z.; Peters, E. M.; Peters, K.; von Schnering, H. G.; Walz, L. Liebigs Ann. 1996, 1055–1081. (c) Kolomeitsev, A. A.; Koppel, I. A.; Rodima, T.; Barten, J.; Lork, E.; Röschenthaler, G.‐V.; Kaljurand, I.; Kütt, A.; Koppel, I.; Mäemets, V.; Leito, I. J. Am. Chem. Soc. 2005, 127, 17656–17666. Also see, refs 81 and 87.
3 3. (a) Marcelli, T.; Hiemstra, H. Synthesis 2010, 1229–1279. (b) Yeboah, E. M. O.; Yeboah, S. O.; Singh, G. S. Tetrahedron 2011, 67, 1725–1762.
4 4. (a) Leow, D.; Tan, C.‐H. Chem. Asian J. 2009, 4, 488–507. (b) Don, S.; Feng, X.; Liu, X. Chem. Soc. Rev. 2018, 47, 8525–8540. (c) Chou, H.‐C.; Leow, D.; Tan, C.‐H. Chem. Asian. J. 2019, 14, 3803–3822.
5 5. (a) Krawczyk, H.; Dzięgielewski, M.; Deredas, D.; Albrecht, A.; Albrecht, Ł. Chem. Eur. J. 2015, 21, 10268–10277. (b) Teng, B.; Lim, W. C.; Tan, C.‐H. Synlett 2017, 28, 1272–1277. (c) Wang, Y.‐H.; Cao, Z.‐Y.; Li, Q.‐H.; Lin, G.‐Q.; Zhou, J.; Tian, P. Angew. Chem. Int. Ed. 2020, 59, 8004–8014.
6 6. Catalytic Asymmetric Synthesis; Ojima, I. Ed.; John Wiley & Sons: New Jersey, 2010, pp 59–94.
7 7. (a) Uraguchi, D.; Koshimoto, K.; Ooi, T. J. Am. Chem. Soc. 2008, 130, 10878–10879. (b) Uraguchi, D.; Oyaizu, K.; Ooi, T. Chem. Eur. J. 2012, 18, 8306–8309. (c) Zhang, W.‐Q.; Cheng, L.‐F.; Yu, J.; Gong, L.‐Z. Angew. Chem. Int. Ed. 2012, 51, 4085–4088. (d) Zhou, X.; Wu, Y.; Deng, L. J. Am. Chem. Soc. 2016, 138, 12297–12302.
8 8. Kondoh, A.; Ishikawa, S.; Terada, M. J. Am. Chem. Soc. 2020, 142, 3724–3728.
9 9. Wynberg, H. Topics in Stereochemistry 1986, 16, 87–129.
10 10. Hiemsta, H.; Wynberg, H. J. Am. Chem. Soc. 1981, 103, 417–430.
11 11. Grayson, M. N.; Houk, K. N. J. Am. Chem. Soc. 2016, 138, 1170–1173.
12 12. Okino, T.; Hoashi, Y.; Takemoto, Y. J. Am. Chem. Soc. 2003, 125, 12672–12673.
13 13. Okino, T.; Hoashi, Y.; Furukawa, T.; Xu, X.; Takemoto, Y. J. Am. Chem. Soc. 2005, 127, 119–125.
14 14. Hamza, A.; Schubert, G.; Soós, T.; Pápai, I. J. Am. Chem. Soc. 2006, 128, 13151–13160.
15 15. Azuma, T.; Kobayashi, Y.; Sakata, K.; Sasamori, T.; Tokitoh, N.; Takemoto, Y. J. Org. Chem. 2014, 79, 1805–1817.
16 16. (a) Miyabe, H.; Takemoto, Y. Bull. Chem. Soc. Jpn. 2008, 81, 785–795. (b) Fang, X.; Wang, C.‐J. Chem. Commun. 2015, 51, 1185–1197. (c) Gandhi, S.; Sivadas, V.; Baire, B. Eur. J. Org. Chem. 2021, 220–234. (d) Han, X.; Kwiatkowski, J.; Xue, F.; Huang, K.‐W.; Lu, Y. Angew. Chem. Int. Ed. 2009, 48, 7604–7607. (e) Probst, N.; Madarász, Á.; Valkonen, A.; Pápai, I.; Rissanen, K.; Neuvonen, A.; Pihko, P. M. Angew. Chem. Int. Ed. 2012, 51, 8495–8499. (f) Yang, C.; Zhang, E.‐G.; Li, X.; Cheng, J.‐P. Angew. Chem. Int. Ed. 2016, 55, 6506–6510.
17 17. (a) Zhu, Y.; Malerich, J. P.; Rawal, V. H. Angew. Chem. Int. Ed. 2010, 49, 153–156. (b) Rombola, M.; Sumaria, C. S.; Montgomery, T. D.; Rawal, V. H. J. Am. Chem. Soc. 2017, 139, 5297–5300. (c) Kimmel, K. L.; Robak, M. T.; Ellman, J. A. J. Am. Chem. Soc. 2009, 131, 8754–8755. (d) Kimmel, K. L.; Weaver, J. D.; Lee, M.; Ellman, J. A. J. Am. Chem. Soc. 2012, 134, 9058–9061. (e) Inokuma, T.; Furukawa, M.; Uno, T.; Suzuki, Y.; Yoshida, K.; Yano, Y.; Matsuzaki, K.; Takemoto, Y. Chem. Eur. J. 2011, 17, 10470–10477.
18 18. (a) Li, B.‐J.; Jiang, L.; Liu, M.; Chen, Y.‐C.; Ding, L.‐S.; Wu, Y. Synlett 2005, 603–606. (b) Vakulya, B.; Varga, S.; Csámpai, A.; Soós, T. Org. Lett. 2005, 7, 1967–1969. (c) McCooey, S. H.; Connon, S. J. Angew. Chem. Int. Ed. 2005, 44, 6367–6370. (d) Ye, J.; Dixon, D. J.; Hynes, P. S. Chem. Commun. 2005, 4481–4483.
19 19. (a) Malerich, J. P.; Hagihara, K.; Rawal, V. H. J. Am. Chem. Soc. 2008, 130, 14416–14417. (b) Zhu, Q.; Lu, Y. Angew. Chem. Int. Ed. 2010, 49, 7753–7756. (c) Ding, M.; Zhou, F.; Liu. Y.‐L.; Wang, C.‐H.; Zhao, X.‐L.; Zhou, J. Chem. Sci. 2011, 2, 2035–2039. (d) Urruzuno, I.; Mugica, O.; Oiarbide, M.; Palomo, C. Angew. Chem. Int. Ed. 2017, 56, 2059–2063. (e) Arai, R.; Hirashima, S.; Kondo, J.; Nakashima, K.; Koseki, Y.; Miura, T. Org. Lett. 2018, 20, 5569–5572.
20 20. (a) Chauhan, P.; Mahajan, S.; Kaya, U.; Hack, D.; Enders, D. Adv. Synth. Catal. 2015, 357, 253–281. (b) Mukhopadhyay, S.; Gharui, C.; Pan, S. C. Asian J. Org. Chem. 2019, 8, 1970–1984. (c) Hou, X.‐Q.; Du, D.‐M. Adv. Synth. Catal. 2020, 362, 4487–4512.
21 21. Li, H.; Wang, Y.; Tang, L.; Deng, L. J. Am. Chem. Soc. 2004, 126, 9906–9907.
22 22. Saaby, S.; Bella, M.; Jørgensen, K. A. J. Am. Chem. Soc. 2004, 126, 8120–8121.
23 23. Li, H.; Wang, Y.; Tang, L.; Wu, F.; Liu, X.; Guo, C.; Foxman, B. M.; Deng, L. Angew. Chem. Int. Ed. 2005, 44, 105–108.
24 24. Marcelli, T.; Haas, R. N. S.; Maarseveen, J. H.; Hiemstra, H. Angew. Chem. Int. Ed. 2006, 45, 929–931.
25 25. Xiao, X.; Xie, Y.; Su, C.; Liu, M.; Shi, Y. J. Am. Chem. Soc. 2011, 133, 12914–12917.
26 26. Tan, B.; Hernández‐Torres, G.; Barbas III, C. F. Angew. Chem. Int. Ed. 2012, 51, 5381–5385.
27 27. Bae, H. Y.; Sim, J. H.; Lee, J.‐W.; List, B.; Song, C. E. Angew. Chem. Int. Ed. 2013, 52, 12143–12147.
28 28. (a) Clerici, P.; Wennemers, H. Org. Biomol. Chem. 2012, 10, 110–113. (b) Bahlinger, A.; Fritz, S. P.; Wennemers, H. Angew. Chem. Int. Ed. 2014, 53, 8779–8783. (c) Engl, O. D.; Fritz, S. P.; Wennemers, H. Angew. Chem. Int. Ed. 2015, 54, 8193–8197.
29 29. (a) Saadi, J.; Wennemers, H. Nature Chem. 2016, 8, 276–280. (b) Cosimi, E.; Engl, O. D.; Saadi, J.; Ebert, M.‐O.; Wennemers, H. Angew. Chem. Int. Ed. 2016, 55, 13127–13131.
30 30. СКАЧАТЬ