Catalytic Asymmetric Synthesis. Группа авторов
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Название: Catalytic Asymmetric Synthesis

Автор: Группа авторов

Издательство: John Wiley & Sons Limited

Жанр: Химия

Серия:

isbn: 9781119736417

isbn:

СКАЧАТЬ

      Source: Based on [87].

      1 1. (a) Hajos, Z. G.; Parrish, D. R. German Patent DE 2102623, 1971. (b) Hajos, Z. G.; Parrish, D. R. J. Org. Chem. 1974, 39, 1615–1621.

      2 2. (a) Eder, U.; Sauer, G.; Wiechert, R. German Patent DE 2014757, 1971. (b) Eder, U.; Sauer, G.; Wiechert, R. Angew. Chem. Int. Ed. 1971, 10, 496–497.

      3 3. (a) List, B.; Lerner, R. A.; Barbas III, C. F. J. Am. Chem. Soc. 2000, 122, 2395–2396. (b) Sakthivel, K.; Notz, W.; Bui, T.; Barbas III, C. F. J. Am. Chem. Soc. 2001, 123, 5260–5267. Review of enamine, see; (c) Mukherjee, S.; Yang, J. W.; Hoffmann, S.; List, B. Chem. Rev. 2007, 107, 5471–5569.

      4 4. (a) Ahrendt, K. A.; Borths, C. J.; MacMillan, D. V. C. J. Am. Chem. Soc. 2000, 122, 4243–4244. Reviews of iminium ion: (b) Lelais, G.; MacMillan, D. W. C. Aldrichimica Acta, 2006, 39, 79–87. (c) Erkkilä, A.; Majander, I.; Pihko, P. M. Chem Rev. 2007, 107, 5416–5470.

      5 5. Selected reviews on organocatalysis: (a) Asymmetric Organocatalysis 1: Lewis Base and Acid Catalysts, (Ed.: B. List) Stuttgart: Thieme, 2012. (b) Asymmetric Organocatalysis 2: Brønsted Base and Acid catalysts, and Additional Topics (Ed.: K. Maruoka) Stuttgart: Thieme, 2012.

      6 6. Watson, A. J. B.; MacMillan, D. W. C. Catalytic Asymmetric Synthesis, 3rd ed, (Ed.: I. Ojima). Hoboken, John Wiley & Sons, 2010, pp. 39–57.

      7 7. Reviews, see: (a) Palomo, C.; Mielgo, A. Angew. Chem. Int. Ed. 2006, 45, 7876–7880. (b) Mielgo, A.; Palomo, C. Chem. Asian J. 2008, 3, 922–948. (c) Xu, L. W.; Li, L.; Shi, Z. H. Adv. Synth. Catal. 2010, 352, 243–279. (d) Jensen, K. L.; Dickmeiss, G.; Jiang, H.; Albrecht, Ł.; Jørgensen, K. A. Acc. Chem. Res. 2012, 4, 248–264. (e) Wróblewska, A. Synlett 2012, 23, 953–954. (f) Gotoh, H.; Hayashi, Y. Sustainable Catalysis (Eds.: Dunn, P. J.; Hii, K. K.; Krische, M. J.; Williams, M. T.) Hoboken: Wiley, 2013, pp. 287–316. (g) Donslund, B. S.; Johansen, T. K.; Poulsen, P. H.; Halskov, K. S.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2015, 54, 13860–13874.

      8 8. Marigo, M.; Wabnitz, T. C.; Fielenbach, D.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2005, 44, 794–797.

      9 9. Hayashi, Y.; Gotoh, H.; Hayashi T.; Shoji, M. Angew. Chem. Int. Ed. 2005, 44, 4212–4215.

      10 10. Reviews: (a) Marcelli, T.; van Maarseveen, J. H.; Hiemstra, H. Angew. Chem. Int. Ed. 2006, 45, 7496–7504. (b) Xu, L.‐W.; Luo, J.; Lu, Y. Chem. Commun. 2009, 1807–1821. (c) Melchiorre, P. Angew. Chem. Int. Ed. 2012, 51, 9748–9770.

      11 11. (a) Lakhdar, S.; Tokuyasu, T.; Mayr, H. Angew. Chem. Int. Ed. 2008, 47, 8723–8726. (b) Mayr, H.; Lakhdar, S.; Maji, B.; Ofial, A. R. Beilstein J. Org. Chem. 2012, 8, 1458–1478. (c) Lakhdar, S.; Maji, B.; Mayr, H. Angew. Chem. Int. Ed. 2012, 51, 5739–5742. (d) An, F.; Maji, B.; Min, E.; Ofial, A. R.; Mayr, H. J. Am. Chem. Soc. 2020, 142, 1526–1547.

      12 12. (a) List, B. Amine‐catalyzed aldol reactions, in: Modern Aldol Reactions (Ed.: R. Mahrwald) Weinheim: Wiley‐VCH, 2004, Chapter 4, pp. 161–200. (b) Mase, N.; Hayashi, Y., The aldol reaction: organocatalysis approach, in: Comprehensive Organic Synthesis, 2nd ed (Eds.: P. Knochel, G. A. Molander) Amsterdam: Elsevier, 2014; Chapter 2.07, pp. 273–339. (c) Yamashita, Y.; Yasukawa, T.; Yoo, W. J.; Kitanosono, T.; Kobayashi, S. Chem. Soc. Rev. 2018, 47, 4388–4480.

      13 13. (a) Bahmanyar, S.; Houk, K. N.; Martin, H. J.; List, B. J. Am. Chem. Soc. 2003, 125, 2475–2479. (b) Allemann, C.; Gordillo, R.; Clemente, F. R.; Cheong, P. H. Y.; Houk, K. N. Acc. Chem. Res. 2004, 37, 558–569.

      14 14. Kano, T.; Yamaguchi, Y.; Tanaka Y.; Maruoka, K. Angew. Chem. Int. Ed. 2007, 46, 1738–1740.

      15 15. Hayashi, Y.; Itoh, T.; Aratake, S.; Ishikawa, H. Angew. Chem. Int. Ed. 2008, 47, 2082–2084.

      16 16. (a) Urushima, T.; Yasui, Y.; Ishikawa, H.; Hayashi, Y. Org. Lett. 2010, 12, 2966–2969. (b) Hayashi, Y.; Yasui, Y.; Kawamura, T.; Kojima, M.; Ishikawa, H. Synlett 2011, 485–488. (c) Hayashi, Y.; Yasui, Y.; Kawamura, T.; Kojima, M.; Ishikawa, H. Angew. Chem. Int. Ed. 2011, 50, 2804–2807. (d) Hayashi, Y.; Yasui, Y.; Kojima, M.; Kawamura, T.; Ishikawa, H. Chem. Commun. 2012, 48, 4570–4572. (e) Hayashi, Y.; Kojima, M. ChemCatChem. 2013, 5, 2883–2885. (f) Hayashi, Y.; Kojima, M.; Yasui, Y.; Kanda, Y.; Mukaiyama, T.; Shomura, H.; Nakamura, D.; Ritmaleni, L.; Sato, I. ChemCatChem. 2013, 5, 2887–2892. (g) Yasui, Y.; Benohoud, M.; Sato, I.; Hayashi, Y. Chem. Lett. 2014, 43, 556–558. (h) Hayashi, Y.; Watanabe, S.; Yasui, Y.; Umemiya, S. ChemCatChem. 2015, 7, 1646–1649. (j) Hayashi, Y.; Nakamura, D.; Yasui, Y.; Iwasaki, K.; Chiba, H. Adv. Synth. Catal. 2016, 358, 2345–2351.

      17 17. (a) List, B. J. Am. Chem. Soc. 2000, 122, 9336–9337.Review of Mannich reaction, see; (b) Verkade, J. M. M.; van Hemert, L. J. C.; Quaedflieg, P. J. L. M.; Rutjes, F. P. J. T. Chem. Soc. Rev. 2008, 37, 29–41.

      18 18. (a) Córdova, A.; Notz, W.; Zhong, G.; Betancort, J. M.; Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1842–1843. (b) Córdova, A.; Watanabe, S.; Tanaka, F.; Notz, W.; Barbas III, C. F. J. Am. Chem. Soc. 2002, 124, 1866–1867.

      19 19. (a) Kano, T.; Yamaguchi, Y.; Tokuda, O.; Maruoka, K. J. Am. Chem. Soc. 2005, 127, 16408–16409. (b) Kano, T.; Yamaguchi, Y.; Maruoka, K. Angew. Chem. Int. Ed. 2009, 48, 1838–1840. (c) Kano, T.; Sakamoto, R.; Akakura, M.; Maruoka, K. J. Am. Chem. Soc. 2012, 134, 7516–7520.

      20 20. (a) A. Córdova, Chem. Comm. 2006, 1760–1762. (b) Hayashi, Y.; Sakamoto, D.; Shomura, H.; Hashizume, D. Chem. Eur. J. 2013, 19, 7678–7681.

      21 21. (a) Marigo, M.; Fielenbach, D.; Braunton, A.; Kjœrsgaard, A.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2005, 44, 3703–3706. (b) Steiner, D. D.; Mase, N.; Barbas III, C. F. Angew. Chem. Int. Ed. 2005, 44, 3706–3710. (c) Beeson, T. D.; MacMillan, D. W. C. J. Am. Chem. Soc. 2005, 127, 8826–8828.

      22 22. (a) Brochu, M. P.; Brown, S. P.; MacMillan, D. W. C. J. Am. Chem. Soc. 2004, 126, 4108–4109. (b) Halland, N.; Braunton, A.; Bachmann, S.; Marigo, M.; Jørgensen, K. A. J. Am. Chem. Soc. 2004, 126, 4790–4791.

      23 23. (a) Bertelsen, S.; Halland, N.; Bachmann, S.; Marigo, M.; Braunton, A.; Jørgensen, K. A. Chem. Commun. 2005, 4821–4823. (b) Kano, T.; Ueda, M.; Maruoka, K. J. Am. Chem. Soc. 2008, 130, 3728–3729.

      24 24. Bøgevig, A.; Juhl, K.; Kumaragurubaran, N.; Zhuang, W.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2002, 41, 1790–1793.

      25 25. (a) Brown, S. P.; Brochu, M. P.; Sinz, C. J.; MacMillan, D. W. C. J. Am. Chem. Soc. 2003, 125, 10808–10809. (b) Zhong, G. Angew. Chem. Int. Ed. 2003, 42, 4247–4250. (c) Bøgevig, A.; Sundén, H.; Córdova, СКАЧАТЬ