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Volume 54, Issue 1
  • ISSN: 0032-1400

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2016-01-01
2024-11-21
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References

  1. “Handbook of Homogeneous Hydrogenation”, eds. J. G. de Vries, C. J. Elsevier, 3 volumes, Wiley-VCH, Weinheim, Germany, 2007 [Google Scholar]
  2. T. Ikariya, I. D. Gridnev, Chem. Rec., 2009, 9, (2), 106 [Google Scholar]
  3. B. Therrien, Coord. Chem. Rev., 2009, 253, (3–4), 493 [Google Scholar]
  4. S. Gaillard, J.-L. Renaud, ChemSusChem, 2008, 1, (6), 505 [Google Scholar]
  5. D. S. Matharu, J. E. D. Martins, M. Wills, Chem. Asian J., 2008, 3, (8–9), 1374 [Google Scholar]
  6. C. Wang, X. F. Wu, J. L. Xiao, Chem. Asian J., 2008, 3, (10), 1750 [Google Scholar]
  7. X. F. Wu, J. Mo, X. H. Li, Z. Hyder, J. L. Xiao, Prog. Nat. Sci., 2008, 18, (6), 639 [Google Scholar]
  8. R. H. Morris, Coord. Chem. Rev., 2008, 252, (21–22), 2381 [Google Scholar]
  9. T. Ikariya, A. J. Blacker, Acc. Chem. Res., 2007, 40, (12), 1300 [Google Scholar]
  10. X. F. Wu, J. L. Xiao, Chem. Commun., 2007, (24), 2449 [Google Scholar]
  11. T. Ikariya, K. Murata, R. Noyori, Org. Biomol. Chem., 2006, 4, (3), 393 [Google Scholar]
  12. S. Gladiali, E. Alberico, Chem. Soc. Rev., 2006, 35, (3), 226 [Google Scholar]
  13. J. S. M. Samec, J. E. Bäckvall, P. G. Andersson, P. Brandt, Chem. Soc. Rev., 2006, 35, (3), 237 [Google Scholar]
  14. J. L. Xiao, X. F. Wu, A. Zanotti-Gerosa, F. Hancock, Chim. Oggi, 2005, 23, (5), 50 [Google Scholar]
  15. S. E. Clapham, A. Hadzovic, R. H. Morris, Coord. Chem. Rev., 2004, 248, (21–24), 2201 [Google Scholar]
  16. K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal., 2003, 345, (1–2), 67 [Google Scholar]
  17. F. Joó, Acc. Chem. Res., 2002, 35, (9), 738 [Google Scholar]
  18. C. Saluzzo, M. Lemaire, Adv. Synth. Catal., 2002, 344, (9), 915 [Google Scholar]
  19. R. Noyori, M. Yamakawa, S. Hashiguchi, J. Org. Chem., 2001, 66, (24), 7931 [Google Scholar]
  20. M. J. Palmer, M. Wills, Tetrahedron: Asymmetry, 1999, 10, (11), 2045 [Google Scholar]
  21. R. Noyori, S. Hashiguchi, Acc. Chem. Res., 1997, 30, (2), 97 [Google Scholar]
  22. M. J. Krische, Y. Sun, Acc. Chem. Res., 2007, 40, (12), 1237 [Google Scholar]
  23. J. K. Liu, X. F. Wu, J. A. Iggo, J. L. Xiao, Coord. Chem. Rev., 2008, 252, (5–7), 782 [Google Scholar]
  24. S.-L. You, Chem. Asian J., 2007, 2, (7), 820 [Google Scholar]
  25. W. von E. Doering, R. W. Young, J. Am. Chem. Soc., 1950, 72, (1), 631 [Google Scholar]
  26. A. Fujii, S. Hashiguchi, N. Uematsu, T. Ikariya, R. Noyori, J. Am. Chem. Soc., 1996, 118, (10), 2521 [Google Scholar]
  27. S. Hashiguchi, A. Fujii, J. Takehara, T. Ikariya, R. Noyori, J. Am. Chem. Soc., 1995, 117, (28), 7562 [Google Scholar]
  28. Z. G. Zhang, P. Rooshenas, H. Hausmann, P. R. Schreiner, Synthesis, 2009, (9), 1531 [Google Scholar]
  29. J. Zhang, P. G. Blazecka, M. M. Bruendl, Y. Huang, J. Org. Chem., 2009, 74, (3), 1411 [Google Scholar]
  30. Y. U. Wu, C. J. Lu, W. J. Shan, X. S. Li, Tetrahedron: Asymmetry, 2009, 20, (5), 584 [Google Scholar]
  31. G. F. Wu, J. L. Zhu, Z. H. Ding, Z. X. Shen, Y. W. Zhang, Tetrahedron Lett., 2009, 50, (4), 427 [Google Scholar]
  32. M. Watanabe, K. Murata, J. Synth. Org. Chem., Jpn., 2009, 67, (4), 397 [Google Scholar]
  33. A. Mikhailine, A. J. Lough, R. H. Morris, J. Am. Chem. Soc., 2009, 131, (4), 1394 [Google Scholar]
  34. N. Meyer, A. J. Lough, R. H. Morris, Chem. Eur. J., 2009, 15, (22), 5605 [Google Scholar]
  35. J. E. D. Martins, G. J. Clarkson, M. Wills, Org. Lett., 2009, 11, (4), 847 [Google Scholar]
  36. R. Jiang, X. L. Sun, W. He, H. Chen, Y. Q. Kuang, Appl. Organomet. Chem., 2009, 23, (5), 179 [Google Scholar]
  37. J. Ito, S. Ujiie, H. Nishiyama, Organometallics, 2009, 28, (2), 630 [Google Scholar]
  38. N. Haraguchi, K. Tsuru, Y. Arakawa, S. Itsuno, Org. Biomol. Chem., 2009, 7, (1), 69 [Google Scholar]
  39. W. Baratta, G. Chelucci, S. Magnolia, K. Siega, P. Rigo, Chem. Eur. J., 2009, 15, (3), 726 [Google Scholar]
  40. Z. Q. Zhou, Y. J. Bian, Heteroatom Chem., 2008, 19, (7), 682 [Google Scholar]
  41. Y.-M. Zhang, P. Liu, H.-L. Zhang, Z.-M. Zhou, Synth. React. Inorg. Met.-Org. Nano-Met. Chem., 2008, 38, (7), 577 [Google Scholar]
  42. L. Zani, L. Eriksson, H. Adolfsson, Eur. J. Org. Chem., 2008, (27), 4655 [Google Scholar]
  43. C. A. Sandoval, Y. H. Li, K. L. Ding, R. Noyori, Chem. Asian J., 2008, 3, (10), 1801 [Google Scholar]
  44. M. Rueping, A. P. Antonchick, Angew. Chem. Int. Ed., 2008, 47, (31), 5836 [Google Scholar]
  45. P. Paredes, J. Diez, M. P. Gamasa, Organometallics, 2008, 27, (11), 2597 [Google Scholar]
  46. F. Michalek, A. Lagunas, C. Jimeno, M. A. Pericàs, J. Mater. Chem., 2008, 18, (39), 4692 [Google Scholar]
  47. J. E. D. Martins, D. J. Morris, B. Tripathi, M. Wills, J. Organomet. Chem., 2008, 693, (23), 3527 [Google Scholar]
  48. C. A. Madrigal, A. García-Fernández, J. Gimeno, E. Lastra, J. Organomet. Chem., 2008, 693, (15), 2535 [Google Scholar]
  49. J. T. Liu, Y. N. Wu, X. S. Li, A. S. C. Chan, J. Organomet. Chem., 2008, 693, (12), 2177 [Google Scholar]
  50. D. L. Liu, F. Xie, X. H. Zhao, W. B. Zhang, Tetrahedron, 2008, 64, (16), 3561 [Google Scholar]
  51. Q. Kang, Z.-A. Zhao, S.-L. You, Org. Lett., 2008, 10, (10), 2031 [Google Scholar]
  52. Z. M. Heiden, B. J. Gorecki, T. B. Rauchfuss, Organometallics, 2008, 27, (7), 1542 [Google Scholar]
  53. S. Guillarme, T. X. M. Nguyen, C. Saluzzo, Tetrahedron: Asymmetry, 2008, 19, (12), 1450 [Google Scholar]
  54. W. Baratta, M. Ballico, G. Chelucci, K. Siega, P. Rigo, Angew. Chem. Int. Ed., 2008, 47, (23), 4362 [Google Scholar]
  55. J. Wettergren, A. B. Zaitsev, H. Adolfsson, Adv. Synth. Catal., 2007, 349, (17–18), 2556 [Google Scholar]
  56. A. Quintard, U. Darbost, F. Vocanson, S. Pellet-Rostaing, M. Lemaire, Tetrahedron: Asymmetry, 2007, 18, (16), 1926 [Google Scholar]
  57. X. H. Huang, J. Y. Ying, Chem. Commun., 2007, (18), 1825 [Google Scholar]
  58. S. Enthaler, B. Hagemann, S. Bhor, G. Anilkumar, M. K. Tse, B. Bitterlich, K. Junge, G. Erre, M. Beller, Adv. Synth. Catal., 2007, 349, (6), 853 [Google Scholar]
  59. F. K. Cheung, C. X. Lin, F. Minissi, A. L. Crivillé, M. A. Graham, D. J. Fox, M. Wills, Org. Lett., 2007, 9, (22), 4659 [Google Scholar]
  60. G. Chen, Y. Xing, H. Zhang, J.-X. Gao, J. Mol. Catal. A: Chem., 2007, 273, (1–2), 284 [Google Scholar]
  61. W. Baratta, G. Chelucci, E. Herdtweck, S. Magnolia, K. Siega, P. Rigo, Angew. Chem. Int. Ed., 2007, 46, (40), 7651 [Google Scholar]
  62. K. Ahlford, A. B. Zaitsev, J. Ekström, H. Adolfsson, Synlett, 2007, (16), 2541 [Google Scholar]
  63. R. V. Wisman, J. G. de Vries, B.-J. Deelman, H. J. Heeres, Org. Process Res. Dev., 2006, 10, (3), 423 [Google Scholar]
  64. C. Wang, C. Q. Li, X. F. Wu, A. Pettman, J. L. Xiao, Angew. Chem. Int. Ed., 2009, 48, (35), 6524 [Google Scholar]
  65. X. F. Wu, J. K. Liu, D. Di Tommaso, J. A. Iggo, C. R. A. Catlow, J. Bacsa, J. L. Xiao, Chem. Eur. J., 2008, 14, (25), 7699 [Google Scholar]
  66. X. F. Wu, X. H. Li, A. Zanotti-Gerosa, A. Pettman, J. K. Liu, A. J. Mills, J. L. Xiao, Chem. Eur. J., 2008, 14, (7), 2209 [Google Scholar]
  67. X. F. Wu, C. Corcoran, S. J. Yang, J. L. Xiao, ChemSusChem, 2008, 1, (1–2), 71 [Google Scholar]
  68. X. F. Wu, “Asymmetric Transfer Hydrogenation and Transfer Hydrogenation in Water”, PhD Thesis, Department of Chemistry, The University of Liverpool, UK, 2007 [Google Scholar]
  69. X. F. Wu, J. K. Liu, X. H. Li, A. Zanotti-Gerosa, F. Hancock, D. Vinci, J. W. Ruan, J. L. Xiao, Angew. Chem. Int. Ed., 2006, 45, (40), 6718 [Google Scholar]
  70. X. F. Wu, X. H. Li, M. McConville, O. Saidi, J. L. Xiao, J. Mol. Catal. A: Chem., 2006, 247, (1–2), 153 [Google Scholar]
  71. X. H. Li, J. Blacker, I. Houson, X. F. Wu, J. L. Xiao, Synlett, 2006, (8), 1155 [Google Scholar]
  72. X. F. Wu, D. Vinci, T. Ikariya, J. L. Xiao, Chem. Commun., 2005, (35), 4447 [Google Scholar]
  73. X. F. Wu, X. G. Li, F. King, J. L. Xiao, Angew. Chem. Int. Ed., 2005, 44, (22), 3407 [Google Scholar]
  74. X. F. Wu, X. G. Li, W. Hems, F. King, J. L. Xiao, Org. Biomol. Chem., 2004, 2, (13), 1818 [Google Scholar]
  75. X. G. Li, X. F. Wu, W. P. Chen, F. E. Hancock, F. King, J. L. Xiao, Org. Lett., 2004, 6, (19), 3321 [Google Scholar]
  76. J. Li, Y. M. Zhang, D. F. Han, Q. Gao, C. Li, J. Mol. Catal. A: Chem., 2009, 298, (1–2), 31 [Google Scholar]
  77. C. Creutz, M. H. Chou, J. Am. Chem. Soc., 2009, 131, (8), 2794 [Google Scholar]
  78. N. A. Cortez, G. Aguirre, M. Parra-Hake, R. Somanathan, Tetrahedron Lett., 2009, 50, (19), 2228 [Google Scholar]
  79. K. Akagawa, H. Akabane, S. Sakamoto, K. Kudo, Tetrahedron: Asymmetry, 2009, 20, (4), 461 [Google Scholar]
  80. Z. Q. Zhou, L. H. Wu, Catal. Commun., 2008, 9, (15), 2539 [Google Scholar]
  81. S. Zeror, J. Collin, J.-C. Fiaud, L. A. Zouioueche, Adv. Synth. Catal., 2008, 350, (1), 197 [Google Scholar]
  82. Z. Xu, J. C. Mao, Y. W. Zhang, J. Guo, J. L. Zhu, Catal. Commun., 2008, 9, (5), 618 [Google Scholar]
  83. A. Schlatter, W.-D. Woggon, Adv. Synth. Catal., 2008, 350, (7–8), 995 [Google Scholar]
  84. J. T. Liu, Y. G. Zhou, Y. N. Wu, X. S. Li, A. S. C. Chan, Tetrahedron: Asymmetry, 2008, 19, (7), 832 [Google Scholar]
  85. Y. Himeda, N. Onozawa-Komatsuzaki, S. Miyazawa, H. Sugihara, T. Hirose, K. Kasuga, Chem. Eur. J., 2008, 14, (35), 11076 [Google Scholar]
  86. N. A. Cortez, G. Aguirre, M. Parra-Hake, R. Somanathan, Tetrahedron: Asymmetry, 2008, 19, (11), 1304 [Google Scholar]
  87. Y. Arakawa, A. Chiba, N. Haraguchi, S. Itsuno, Adv. Synth. Catal., 2008, 350, (14–15), 2295 [Google Scholar]
  88. E. Alza, A. Bastero, S. Jansat, M. A. Pericàs, Tetrahedron: Asymmetry, 2008, 19, (3), 374 [Google Scholar]
  89. K. Akagawa, H. Akabane, S. Sakamoto, K. Kudo, Org. Lett., 2008, 10, (10), 2035 [Google Scholar]
  90. K. Ahlford, J. Lind, L. Mäler, H. Adolfsson, Green Chem., 2008, 10, (8), 832 [Google Scholar]
  91. H.-F. Zhou, Q.-H. Fan, Y.-Y. Huang, L. Wu, Y.-M. He, W.-J. Tang, L.-Q. Gu, A. S. C. Chan, J. Mol. Catal. A: Chem., 2007, 275, (1–2), 47 [Google Scholar]
  92. L. Li, J. S. Wu, F. Wang, J. Liao, H. Zhang, C. X. Lian, J. Zhu, J. G. Deng, Green Chem., 2007, 9, (1), 23 [Google Scholar]
  93. N. A. Cortez, G. Aguirre, M. Parra-Hake, R. Somanathan, Tetrahedron Lett., 2007, 48, (25), 4335 [Google Scholar]
  94. J. Canivet, G. Süss-Fink, P. Štepnicka, Eur. J. Inorg. Chem., 2007, (30), 4736 [Google Scholar]
  95. J. Canivet, G. Süss-Fink, Green Chem., 2007, 9, (4), 391 [Google Scholar]
  96. S. Zeror, J. Collin, J.-C. Fiaud, L. A. Zouioueche, J. Mol. Catal. A: Chem., 2006, 256, (1–2), 85 [Google Scholar]
  97. Y. Xing, J.-S. Chen, Z.-R. Dong, Y.-Y. Li, J.-X. Gao, Tetrahedron Lett., 2006, 47, (26), 4501 [Google Scholar]
  98. J. S. Wu, F. Wang, Y. P. Ma, X. C. Cui, L. F. Cun, J. Zhu, J. G. Deng, B. L. Yu, Chem. Commun., 2006, (16), 1766 [Google Scholar]
  99. A. Rossin, G. Kovács, G. Ujaque, A. Lledós, F. Joó, Organometallics, 2006, 25, (21), 5010 [Google Scholar]
  100. M. C. Pirrung, Chem. Eur. J., 2006, 12, (5), 1312 [Google Scholar]
  101. D. S. Matharu, D. J. Morris, G. J. Clarkson, M. Wills, Chem. Commun., 2006, (30), 3232 [Google Scholar]
  102. B.-Z. Li, J.-S. Chen, Z.-R. Dong, Y.-Y. Li, Q.-B. Li, J.-X. Gao, J. Mol. Catal. A: Chem., 2006, 258, (1–2), 113 [Google Scholar]
  103. L. Jiang, T.-F. Wu, Y.-C. Chen, J. Zhu, J.-G. Deng, Org. Biomol. Chem., 2006, 4, (17), 3319 [Google Scholar]
  104. D. M. Jiang, J. S. Gao, Q. H. Yang, J. Yang, C. Li, Chem. Mater., 2006, 18, (25), 6012 [Google Scholar]
  105. N. A. Cortez, R. Rodríguez-Apodaca, G. Aguirre, M. Parra-Hake, T. Cole, R. Somanathan, Tetrahedron Lett., 2006, 47, (48), 8515 [Google Scholar]
  106. Y. Arakawa, N. Haraguchi, S. Itsuno, Tetrahedron Lett., 2006, 47, (19), 3239 [Google Scholar]
  107. F. Wang, H. Liu, L. F. Cun, J. Zhu, J. G. Deng, Y. Z. Jiang, J. Org. Chem., 2005, 70, (23), 9424 [Google Scholar]
  108. J. C. Mao, B. S. Wan, F. Wu, S. W. Lu, Tetrahedron Lett., 2005, 46, (43), 7341 [Google Scholar]
  109. P.-N. Liu, P.-M. Gu, J.-G. Deng, Y.-Q. Tu, Y.-P. Ma, Eur. J. Org. Chem., 2005, (15), 3221 [Google Scholar]
  110. C. Letondor, N. Humbert, T. R. Ward, PNAS, 2005, 102, (13), 4683 [Google Scholar]
  111. J. Canivet, G. Labat, H. Stoeckli-Evans, G. Süss-Fink, Eur. J. Inorg. Chem., 2005, (22), 4493 [Google Scholar]
  112. P. N. Liu, J. G. Deng, Y. Q. Tu, S. H. Wang, Chem. Commun., 2004, (18), 2070 [Google Scholar]
  113. Y. P. Ma, H. Liu, L. Chen, X. Cui, J. Zhu, J. E. Deng, Org. Lett., 2003, 5, (12), 2103 [Google Scholar]
  114. Y. Himeda, N. Onozawa-Komatsuzaki, H. Sugihara, H. Arakawa, K. Kasuga, J. Mol. Catal. A: Chem., 2003, 195, (1–2), 95 [Google Scholar]
  115. H. Y. Rhyoo, H.-J. Park, W. H. Suh, Y. K. Chung, Tetrahedron Lett., 2002, 43, (2), 269 [Google Scholar]
  116. T. Thorpe, J. Blacker, S. M. Brown, C. Bubert, J. Crosby, S. Fitzjohn, J. P. Muxworthy, J. M. J. Williams, Tetrahedron Lett., 2001, 42, (24), 4041 [Google Scholar]
  117. H. Y. Rhyoo, H.-J. Park, Y. K. Chung, Chem. Commun., 2001, (20), 2064 [Google Scholar]
  118. C. Bubert, J. Blacker, S. M. Brown, J. Crosby, S. Fitzjohn, J. P. Muxworthy, T. Thorpe, J. M. J. Williams, Tetrahedron Lett., 2001, 42, (24), 4037 [Google Scholar]
  119. T. Poth, H. Paulus, H. Elias, C. Dücker-Benfer, R. van Eldik, Eur. J. Inorg. Chem., 2001, (5), 1361 [Google Scholar]
  120. X. G. Li, W. P. Chen, W. Hems, F. King, J. L. Xiao, Tetrahedron Lett., 2004, 45, (5), 951 [Google Scholar]
  121. X. G. Li, W. P. Chen, W. Hems, F. King, J. L. Xiao, Org. Lett., 2003, 5, (24), 4559 [Google Scholar]
  122. K.-J. Haack, S. Hashiguchi, A. Fujii, T. Ikariya, R. Noyori, Angew. Chem. Int. Ed., 1997, 36, (3), 285 [Google Scholar]
  123. K. Mashima, T. Abe, K. Tani, Chem. Lett., 1998, (12), 1199 [Google Scholar]
  124. A. J. Blacker, B. J. Mellor, Zeneca Ltd,, ‘Transfer Hydrogenation Process and Catalyst’, World Appl. WO98/42643 [Google Scholar]
  125. J. Blacker, J. Martin, E. Schmidt, ‘Scale-Up Studies in Asymmetric Transfer Hydrogenation’, in “Asymmetric Catalysis on Industrial Scale: Challenges, Approaches and Solutions”, eds. H. U. Blaser, Wiley-VCH, Weinheim, Germany, 2004, pp. 201216 [Google Scholar]
  126. K. Tanaka, M. Katsurada, F. Ohno, Y. Shiga, M. Oda, M. Miyagi, J. Takehara, K. Okano, J. Org. Chem., 2000, 65, (2), 432 [Google Scholar]
  127. M. Miyagi, J. Takehara, S. Collet, K. Okano, Org. Process Res. Dev., 2000, 4, (5), 346 [Google Scholar]
  128. J. S. M. Samec, A. H. Ell, J. B. Åberg, T. Privalov, L. Eriksson, J. E. Bäckvall, J. Am. Chem. Soc., 2006, 128, (44), 14293 [Google Scholar]
  129. Z. M. Heiden, T. B. Rauchfuss, J. Am. Chem. Soc., 2009, 131, (10), 3593 [Google Scholar]
  130. J.-W. Handgraaf, E. J. Meijer, J. Am. Chem. Soc., 2007, 129, (11), 3099 [Google Scholar]
  131. Z. M. Heiden, T. B. Rauchfuss, J. Am. Chem. Soc., 2007, 129, (46), 14303 [Google Scholar]
  132. Z. M. Heiden, T. B. Rauchfuss, J. Am. Chem. Soc., 2006, 128, (40), 13048 [Google Scholar]
  133. S. Arita, T. Koike, Y. Kayaki, T. Ikariya, Angew. Chem. Int. Ed., 2008, 47, (13), 2447 [Google Scholar]
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