Enantioselective synthesis of alcohols and amines by iridium-catalyzed hydrogenation, transfer hydrogenation, and related processes

Chemistry - A European Journal

Volumn 19, Issue 23, 2013, Pages 7274-7302

  Bartoszewicz, Agnieszka ^a,b   Ahlsten, Nanna ^a,b   Martín Matute, Belén ^a,b  

^a STOCKHOLM UNIVERSITY   (Sweden)

^b STOCKHOLM UNIVERSITY   (Sweden)

Author keywords

asymmetric catalysis; hydrogenation; iridium; oxidation; transfer hydrogenation

Indexed keywords

ASYMMETRIC CATALYSIS; BUILDING BLOCKES; CHEMICAL BUILDING BLOCKS; ENANTIOPURE ALCOHOLS; ENANTIOSELECTIVE SYNTHESIS; IRIDIUM CATALYSIS; KINETIC RESOLUTION; TRANSFER HYDROGENATIONS;

AMINES; CATALYSIS; FORMIC ACID; HYDROGEN; IRIDIUM; IRIDIUM COMPOUNDS; KETONES; OXIDATION; STEREOCHEMISTRY;

HYDROGENATION;

ALCOHOL DERIVATIVE; AMINE; FORMIC ACID DERIVATIVE; IMINE; IRIDIUM; KETONE;

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; HYDROGENATION; OXIDATION REDUCTION REACTION; REVIEW; STEREOISOMERISM; SYNTHESIS;

ALCOHOLS; AMINES; CATALYSIS; FORMATES; HYDROGENATION; IMINES; IRIDIUM; KETONES; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 84878221209     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202836     Document Type: Review

References (377)

1. H.-U. Blaser, C. Malan, B. Pugin, F. Spindler, H. Steiner, M. Studer, Adv.Synth. Cat. 2003, 345, 103-151
2. Y. G. Zhou, Acc. Chem. Res. 2007, 40, 1357-1366
3. T. C. Nugent, M. El-Shazly, Adv. Synth. Catal. 2010, 352, 753-819
4. N. Fleury-Brégeot, V. de La Fuente, S. Castillõn, C. Claver, ChemCatChem 2010, 2, 1346-1371
5. A. Fabrello, A. Bachelier, M. Urrutigoïty, P. Kalck, Coord. Chem. Rev. 2010, 254, 273-287
6. M. Diéguez, O. Pàmies, C. Claver, Topics in Organometallic Chemistry, Vol. 34 (Ed.:, P. G. Andersson,), Springer, Berlin/Heidelberg, 2011, pp. 11-29
7. J.-H. Xie, S.-F. Zhu, Q.-L. Zhou, Chem. Rev. 2011, 111, 1713-1760
8. V. Sridharan, P. A. Suryavanshi, J. C. Menéndez, Chem. Rev. 2011, 111, 7157-7259
9. D.-S. Wang, Q.-A. Chen, S.-M. Lu, Y.-G. Zhou, Chem. Rev. 2012, 112, 2257-2590
10. Z. Yu, W. Jin, Q. Jiang, Angew. Chem. 2012, 124, 6164-6177
11. Angew. Chem. Int. Ed. 2012, 51, 6060-6072.
12. S. Kobayashi, H. Ishitani, Chem. Rev. 1999, 99, 1069-1094
13. M. Wills, in Modern Reduction Methods (Eds.:, P. G. Andersson, I. J. Munslow,), Wiley-VCH, Weinheim, 2008, pp. 271-296.
14. G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069
15. R. Noyori, S. Hashiguchi, Acc. Chem. Res. 1997, 30, 97-102
16. M. J. Palmer, M. Wills, Tetrahedron: Asymmetry 1999, 10, 2045-2061
17. R. Noyori, T. Ohkuma, Angew. Chem. 2001, 113, 40-75
18. Angew. Chem. Int. Ed. 2001, 40, 40-73
19. R. Noyori, M. Kitamura, T. Ohkuma, Proc. Natl. Acad. Sci. USA 2004, 101, 5356-5362
20. W. Tang, X. Zhang, Chem. Rev. 2003, 103, 3029-3070
21. T. Ikariya, A. J. Blacker, Acc. Chem. Res. 2007, 40, 1300-1308
22. Iridium Complexes in Organic Synthesis. (Eds.:, L. A. Oro, C. Claver,), Wiley-VCH, Weinheim, Weinheim (Germany), 2009
23. R. Malacea, R. Poli, E. Manoury, Coord. Chem. Rev. 2010, 254, 729-752
24. O. Saidi, J. Williams, Topics in Organometallic Chemistry, Vol. 34 (Ed.:, P. G. Andersson,), Springer, Berlin/Heidelberg, 2011, pp. 77-106
25. J. Václavík, P. Kacer, M. Kuzma, L. Cerveny, Molecules 2011, 16, 5460-5495.
26. X. Cui, K. Burgess, Chem. Rev. 2005, 105, 3272-3296
27. K. Källström, I. Munslow, P. G. Andersson, Chem. Eur. J. 2006, 12, 3194-3200
28. S. J. Roseblade, A. Pfaltz, Acc. Chem. Res. 2007, 40, 1402-1411
29. T. L. Church, P. G. Andersson, Coord. Chem. Rev. 2008, 252, 513-531
30. D. H. Woodmansee, A. Pfaltz, Top. Organomet. Chem. 2011, 34, 31-76
31. D. H. Woodmansee, A. Pfaltz, Chem. Commun. 2011, 47, 7912-7916
32. A. Cadu, P. G. Andersson, J. Organomet. Chem. 2012, 714, 3-11.
33. F. Spindler, B. Pugin, H. P. Jalett, H. P. Buser, U. Pittelkow, H.-U. Blaser, Catalysis of Organic Reactions, Vol. 68 (Ed.:, R. E. Malz,), Marcel Dekker, New York, 1996, pp. 153-166
34. H. U. Blaser, F. Spindler, Top Cat. 1997, 4, 275-282
35. H.-U. Blaser, Adv. Synth. Catal. 2002, 344, 17-31
36. H.-U. Blaser, B. Pugin, F. Spindler, M. Thommen, Acc. Chem. Res. 2007, 40, 1240-1250.
37. C. A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1992, 114, 7562-7564
38. C. A. Willoughby, S. L. Buchwald, J. Org. Chem. 1993, 58, 7627-7629
39. C. A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 8952-8965
40. C. A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 11703-11714.
41. M. Ringwald, R. Stürmer, H. H. Brintzinger, J. Am. Chem. Soc. 1999, 121, 1524-1527.
42. M. J. Burk, J. E. Feaster, J. Am. Chem. Soc. 1992, 114, 6266-6267
43. F. Spindler, H.-U. Blaser, Adv. Synth. Catal. 2001, 343, 68-70
44. G. Shang, Q. Yang, X. Zhang, Angew. Chem. 2006, 118, 6508-6510
45. Angew. Chem. Int. Ed. 2006, 45, 6360-6362
46. C. Li, J. Xiao, J. Am. Chem. Soc. 2008, 130, 13208-13209
47. N. Pannetier, J.-B. Sortais, J.-T. Issenhuth, L. Barloy, C. Sirlin, A. Holuigue, L. Lefort, L. Panella, J. G. de Vries, M. Pfeffer, Adv. Synth. Catal. 2011, 353, 2844-2852.
48. Q. Yang, G. Shang, W. Gao, J. Deng, X. Zhang, Angew. Chem. 2006, 118, 3916-3919
49. Angew. Chem. Int. Ed. 2006, 45, 3832-3835
50. Y.-Q. Wang, C.-B. Yu, D.-W. Wang, X.-B. Wang, Y.-G. Zhou, Org. Lett. 2008, 10, 2071-2074
51. C.-B. Yu, D.-W. Wang, Y.-G. Zhou, J. Org. Chem. 2009, 74, 5633-5635
52. C.-B. Yu, K. Gao, D.-S. Wang, L. Shi, Y.-G. Zhou, Chem. Commun. 2011, 47, 5052-5054.
53. C. J. Cobley, J. P. Henschke, Adv. Synth. Catal. 2003, 345, 195-201
54. H. Zhou, Z. Li, Z. Wang, T. Wang, L. Xu, Y. He, Q.-H. Fan, J. Pan, L. Gu, A. S. C. Chan, Angew. Chem. 2008, 120, 8592-8595
55. Angew. Chem. Int. Ed. 2008, 47, 8464-8467
56. Z.-J. Wang, H.-F. Zhou, T.-L. Wang, Y.-M. He, Q.-H. Fan, Green Chem. 2009, 11, 767-769
57. F. Chen, Z. Ding, J. Qin, T. Wang, Y. He, Q.-H. Fan, Org. Lett. 2011, 13, 4348-4351
58. T. Wang, L.-G. Zhuo, Z. Li, F. Chen, Z. Ding, Y. He, Q.-H. Fan, J. Xiang, Z.-X. Yu, A. S. C. Chan, J. Am. Chem. Soc. 2011, 133, 9878-9891
59. F. Chen, T. Wang, Y. He, Z. Ding, Z. Li, L. Xu, Q.-H. Fan, Chem. Eur. J. 2011, 17, 1109-1113.
60. C. González-Arellano, A. Corma, M. Iglesias, F. Sánchez, Chem. Commun. 2005, 3451-3453.
61. N. Uematsu, A. Fujii, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1996, 118, 4916-4917
62. A. Fujii, S. Hashiguchi, N. Uematsu, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1996, 118, 2521-2522
63. E. Vedejs, P. Trapencieris, E. Suna, J. Org. Chem. 1999, 64, 6724-6729
64. Y.-C. Chen, T.-F. Wu, J.-G. Deng, H. Liu, X. Cui, J. Zhu, Y.-Z. Jiang, M. C. K. Choi, A. S. C. Chan, J. Org. Chem. 2002, 67, 5301-5306
65. J. Wu, F. Wang, Y. Ma, X. Cui, L. Cun, J. Zhu, J. Deng, B. Yu, Chem. Commun. 2006, 1766-1768
66. N. Haraguchi, K. Tsuru, Y. Arakawa, S. Itsuno, Org. Biomol. Chem. 2009, 7, 69-75.
67. J. Mao, D. C. Baker, Org. Lett. 1999, 1, 841-843
68. L. Li, J. Wu, F. Wang, J. Liao, H. Zhang, C. Lian, J. Zhu, J. Deng, Green Chem. 2007, 9, 23-25.
69. S. Zhou, S. Fleischer, K. Junge, S. Das, D. Addis, M. Beller, Angew. Chem. 2010, 122, 8224-8224
70. Angew. Chem. Int. Ed. 2010, 49, 8048-8048
71. A. A. Mikhailine, M. I. Maishan, R. H. Morris, Org. Lett. 2012, 14, 4638-4641.
72. V. Herrera, B. Muñoz, V. Landaeta, N. Canudas, J. Mol. Catal. A 2001, 174, 141-149
73. V. R. Landaeta, B. K. Muñoz, M. Peruzzini, V. Herrera, C. Bianchini, R. A. Sánchez-Delgado, Organometallics 2005, 24, 403-409
74. V. R. Landaeta, M. Peruzzini, V. Herrera, C. Bianchini, R. A. Sánchez-Delgado, A. E. Goeta, F. Zanobini, J. Organomet. Chem. 2006, 691, 1039-1050
75. M. Martín, E. Sola, S. Tejero, J. L. Andrés, L. A. Oro, Chem. Eur. J. 2006, 12, 4043-4056
76. M. Martín, E. Sola, S. Tejero, J. A. Lõpez, L. A. Oro, Chem. Eur. J. 2006, 12, 4057-4068
77. K. H. Hopmann, A. Bayer, Organometallics 2011, 30, 2483-2497.
78. K. Fagnou, M. Lautens, K. Fagnou, M. Lautens, Angew. Chem. 2002, 114, 26-49
79. Angew. Chem. Int. Ed. 2002, 41, 26-47.
80. A. Levi, G. Modena, G. J. Scorrano, Chem. Soc. Chem. Commun. 1975, 6-7.
81. S. Vastag, J. Bakos, S. Toros, N. E. Takach, R. B. King, B. Heil, L. Marko, J. Mol. Catal. 1984, 22, 283-287
82. G.-J. Kang, W. R. Cullen, M. D. Fryzuk, B. R. James, J. P. Kutney, J. Chem. Soc. Chem. Commun. 1988, 1466-1467
83. J. Bakos, I. Toth, B. Heil, G. Szalontai, L. Parkanyi, V. Fulop, J. Organomet. Chem. 1989, 370, 263-276.
84. Y. Ng, C. Chan, J. A. Osborn, J. Am. Chem. Soc. 1990, 112, 9400-9401
85. F. Spindler, B. Pugin, H.-U. Blaser, Angew. Chem. 1990, 102, 561-562
86. Angew. Chem. Int. Ed. Engl. 1990, 29, 558-559.
87. R. Sablong, J. A. Osborn, Tetrahedron: Asymmetry 1996, 7, 3059-3062.
88. T. Morimoto, N. Nakajima, K. Achiwa, Chem. Pharm. Bull. 1994, 42, 1951-1953.
89. K. Tani, J. Onouchi, Y. Yamagata, Y. Kataoka, Chem. Lett. 1995, 955-956.
90. E. Peris, J. C., Jr. Lee, J. R. Rambo, O. Eisenstein, R. H. Crabtree, J. Am. Chem. Soc. 1995, 117, 3485-3491.
91. T. Morimoto, N. Nakajima, K. Achiwa, Synlett 1995, 748-750.
92. T. Morimoto, K. Achiwa, Tetrahedron: Asymmetry 1995, 6, 2661-2664.
93. T. Morimoto, N. Suzuki, K. Achiwa, Tetrahedron: Asymmetry 1998, 9, 183-187.
94. A. Togni, C. Breutel, A. Schnyder, F. Spindler, H. Landert, A. Tijani, J. Am. Chem. Soc. 1994, 116, 4062-4066.
95. H.-U. Blaser, H.-P. Buser, R. Hausel, H.-P. Jalett, F. Spindler, J. Organomet. Chem. 2001, 621, 34-38.
96. B. Pugin, H. Landert, F. Spindler, H.-U. Blaser, Adv. Synth. Catal. 2002, 344, 974-979.
97. H.-U. Blaser, B. Pugin, F. Spindler, A. Togni, C. R. Chim. 2002, 5, 379-385.
98. R. H. Crabtree, Acc. Chem. Res. 1979, 12, 331-338.
99. M. T. Reetz, E. W. Beuttenmüller, R. Goddard, M. Pastõ, Tetrahedron Lett. 1999, 40, 4977-4980.
100. D. Xiao, X. Zhang, Angew. Chem. 2001, 113, 3533-3536
101. Angew. Chem. Int. Ed. 2001, 40, 3425-3428.
102. M. Chang, W. Li, X. Zhang, Angew. Chem. 2011, 123, 10867-10869
103. Angew. Chem. Int. Ed. 2011, 50, 10679-10681.
104. Iodine-bridged complexes:, T. Yamagata, H. Tadaoka, M. Nagata, T. Hirao, Y. Kataoka, V. Ratovelomanana-Vidal, J.-P. Genêt, K. Mashima, Organometallics 2006, 25, 2505-2513.
105. During the preparation of this article, another Ir system using Synphos-derived ligands targeting the reduction of substrate 13 was reported:, F. Berhal, Z. Wu, Z. Zhang, T. Ayad, V. Ratovelomanana-Vidal, Org. Lett. 2012, 14, 3308-3311.
106. A. Dervisi, C. Carcedo, L.-L. Ooi, Adv. Synth. Catal. 2006, 348, 175-183.
107. T. Imamoto, N. Iwadate, K. Yoshida, Org. Lett. 2006, 8, 2289-2292.
108. S. Vargas, M. Rubio, A. Suárez, A. Pizzano, Tetrahedron Lett. 2005, 46, 2049-2052.
109. E. Guiu, M. Aghmiz, Y. Díaz, B. Muñoz, C. Claver, B. Meseguer, C. Militzer, S. Castillõn, Eur. J. Org. Chem. 2006, 627-633.
110. E. Guiu, B. Muñoz, S. Castillõn, C. Claver, Adv. Synth. Catal. 2003, 345, 169-171.
111. W.-B. Wang, S.-M. Lu, P.-Y. Yang, X.-W. Han, Y.-G. Zhou, J. Am. Chem. Soc. 2003, 125, 10536-10537.
112. X. B. Wang, Y. G. Zhou, J. Org. Chem. 2008, 73, 5640-5642.
113. S. M. Lu, Y. Q. Wang, X. W. Han, Y. G. Zhou, Angew. Chem. 2006, 118, 2318-2321
114. Angew. Chem. Int. Ed. 2006, 45, 2260-2263.
115. D.-S. Wang, Y.-G. Zhou, Tetrahedron Lett. 2010, 51, 3014-3017.
116. L. Shi, Z.-S. Ye, L.-L. Cao, R.-N. Guo, Y. Hu, Y.-G. Zhou, Angew. Chem. Int. Ed. 2012, 51, 8411-8414
117. Angew. Chem. Int. Ed. 2012, 124, 8286-8289.
118. H. Tadaoka, D. Cartigny, T. Nagano, T. Gosavi, T. Ayad, J.-P. Genêt, T. Ohshima, V. Ratovelomanana-Vidal, K. Mashima, Chem. Eur. J. 2009, 15, 9990-9994.
119. C. Deport, M. Buchotte, K. Abecassis, H. Tadaoka, T. Ayael, T. Ohshima, J. P. Genêt, K. Mashima, V. Ratovelomanana-Vidal, Synlett 2007, 2743-2747.
120. W. Tang, Y. Sun, L. Xu, T. Wang, Q. Fan, K. Lam, A. S. C. Chan, Org. Biomol. Chem. 2010, 8, 3464-3471.
121. D.-W. Wang, X.-B. Wang, D.-S. Wang, S.-M. Lu, Y.-G. Zhou, Y.-X. Li, J. Org. Chem. 2009, 74, 2780-2787.
122. X.-B. Wang, W. Zeng, Y.-G. Zhou, Tetrahedron Lett. 2008, 49, 4922-4924.
123. Z.-S. Ye, M.-W. Chen, Q.-A. Chen, L. Shi, Y. Duan, Y.-G. Zhou, Angew. Chem. 2012, 124, 10328-10331
124. Angew. Chem. Int. Ed. 2012, 51, 10181-10184.
125. L. K. Xu, K. H. Lam, J. X. Ji, J. Wu, Q. H. Fan, W. H. Lo, A. S. C. Chan, Chem. Commun. 2005, 1390-1392.
126. S. H. Chan, K. H. Lam, Y.-M. Li, L. Xu, W. Tang, F. L. Lam, W. H. Lo, W. Y. Yu, Q. Fan, A. S. C. Chan, Tetrahedron: Asymmetry 2007, 18, 2625-2631.
127. Z.-J. Wang, G.-J. Deng, Y. Li, Y.-M. He, W.-J. Tang, Q.-H. Fan, Org. Lett. 2007, 9, 1243-1246.
128. L. Qiu, F. Y. Kwong, J. Wu, W. H. Lam, S. Chan, W. Y. Yu, Y. M. Li, R. Guo, Z. Zhou, A. S. C. Chan, J. Am. Chem. Soc. 2006, 128, 5955-5965.
129. W. Tang, L. Xu, Q.-H. Fan, J. Wang, B. Fan, Z. Zhou, K.-H. Lam, A. S. C. Chan, Angew. Chem. 2009, 121, 9299-9302
130. Angew. Chem. Int. Ed. 2009, 48, 9135-9138.
131. K. H. Lam, L. Xu, L. Feng, Q. H. Fan, F. L. Lam, W. H. Lo, A. S. C. Chan, Adv. Synth. Catal. 2005, 347, 1755-1758.
132. M. T. Reetz, X. Li, Chem. Commun. 2006, 2159-2160.
133. M. Eggenstein, A. Thomas, J. Theuerkauf, G. Franciò, W. Leitner, Adv. Synth. Catal. 2009, 351, 725-732.
134. J. L. Núñez-Rico, H. Fernández-Pérez, J. Benet-Buchholz, A. Vidal-Ferran, Organometallics 2010, 29, 6627-6631.
135. C.-J. Hou, Y.-H. Wang, Z. Zheng, J. Xu, X.-P. Hu, Org. Lett. 2012, 14, 3554-3557.
136. K. Gao, C.-B. Yu, W. Li, Y-G. Zhou, X. Zhang, Chem. Commun. 2011, 47, 7845-7847.
137. K. Gao, B. Wu, C.-B. Yu, Q.-A. Chen, Z.-S. Ye, Y.-G. Zhou, Org. Lett. 2012, 14, 3890-3893.
138. P. Schnider, G. Koch, R. Prétôt, G. Wang, F. M. Bohnen, C. Krüger, A. Pfaltz, Chem. Eur. J. 1997, 3, 887-892.
139. R. H. Crabtree, G. E. Morris, J. Organomet. Chem. 1977, 135, 395-403.
140. S. Kainz, A. Brinkmann, W. Leitner, A. Pfaltz, J. Am. Chem. Soc. 1999, 121, 6421-6429
141. F. Menges, A. Pfaltz, Adv. Synth. Catal. 2002, 344, 40-44.
142. S. P. Smidt, N. Zimmermann, M. Studer, A. Pfaltz, Chem. Eur. J. 2004, 10, 4685-4693
143. S. P. Smidt, A. Pfaltz, E. Martínez-Viviente, P. S. Pregosin, A. Albinati, Organometallics 2003, 22, 1000-1009.
144. C. Blanc, F. Agbossou-Niedercorn, G. Nowogrocki, Tetrahedron: Asymmetry 2004, 15, 2159-2163.
145. A. Trifonova, J. S. Diesen, C. J. Chapman, P. G. Andersson, Org. Lett. 2004, 6, 3825-3827.
146. A. Trifonova, J. S. Diesen, P. G. Andersson, Chem. Eur. J. 2006, 12, 2318-2328.
147. S.-F. Zhu, J.-B. Xie, Y.-Z. Zhang, S. Li, Q.-L. Zhou, J. Am. Chem. Soc. 2006, 128, 12886-12891.
148. Z. Han, Z. Wang, X. Zhang, K. Ding, Angew. Chem. 2006, 118, 5449-5453
149. Angew. Chem. Int. Ed. 2009, 48, 5345-5349.
150. A. Baeza, A. Pfaltz, Chem. Eur. J. 2009, 15, 2266-2269
151. M. G. Schrems, A. Pfaltz, Chem. Commun. 2009, 6210-6212.
152. A. Baeza, A. Pfaltz, Chem. Eur. J. 2010, 16, 4003-4009.
153. C. Moessner, C. Bolm, Angew. Chem. 2005, 117, 7736-7739
154. Angew. Chem. Int. Ed. 2005, 44, 7564-7567.
155. S.-M. Lu, X.-W. Han, Y.-G. Zhou, Adv. Synth. Catal. 2004, 346, 909-912.
156. D.-S. Wang, J. Zhou, D.-W. Wang, Y.-L. Guo, Y.-G. Zhou, Tetrahedron Lett. 2010, 51, 525-528.
157. M. N. Cheemala, P. Knochel, Org. Lett. 2007, 9, 3089-3092.
158. X.-B. Jiang, A. J. Minnaard, B. Hessen, B. L. Feringa, A. L. L. Duchateau, J. G. O. Andrien, J. A. F. Boogers, J. G. de Vries, Org. Lett. 2003, 5, 1503-1506.
159. M. T. Reetz, O. Bondarev, Angew. Chem. 2007, 119, 4607-4610
160. Angew. Chem. Int. Ed. 2007, 46, 4523-4526.
161. M. T. Reetz, A. Meiswinkel, G. Mehler, K. Angermund, M. Graf, W. Thiel, R. Mynott, D. G. Blackmond, J. Am. Chem. Soc. 2005, 127, 10305-10313
162. I. D. Gridnev, C. Fan, P. G. Pringle, Chem. Commun. 2007, 1319-1321.
163. M. T. Reetz, T. Sell, A. Meiswinkel, G. Mehler, Angew. Chem. 2003, 115, 814-817
164. Angew. Chem. Int. Ed. 2003, 42, 790-793.
165. N. Mršic̈, L. Lefort, J. A. F. Boogers, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Adv. Synth. Catal. 2008, 350, 1081-1089.
166. N. Mršic̈, T. Jerphagnon, A. J. Minnaard, B. L. Feringa, J. G. de Vries, Adv. Synth. Catal. 2009, 351, 2549-2552.
167. N. Mršic̈, A. J. Minnaard, B. L. Feringa, J. G. de Vries, J. Am. Chem. Soc. 2009, 131, 8358-8359.
168. N. Mršic̈, L. Panella, E. G. IJpeij, A. J. Minnaard, B. L. Feringa, J. G. de Vries, ChemCatChem 2011, 3, 1139-1142.
169. S. E. Lyubimov, E. A. Rastorguev, P. V. Petrovskii, E. S. Kelbysheva, N. M. Loim, V. A. Davankov, Tetrahedron Lett. 2011, 52, 1395-1397.
170. J.-H. Xie, P.-C. Yan, Q.-Q. Zhang, K.-X. Yuan, Q.-L. Zhou, ACS Catal. 2012, 2, 561-564.
171. G. Hou, R. Tao, Y. Sun, X. Zhang, F. Gosselin, J. Am. Chem. Soc. 2010, 132, 2124-2125.
172. T. Ikariya, K. Murata, R. Noyori, Org. Biomol. Chem. 2006, 4, 393-406
173. M. Ito, T. Ikariya, Chem. Commun. 2007, 5134-5142
174. H. Arita, K. Ishiwata, S. Kuwata, T. Ikariya, Organometallics 2008, 27, 493-496
175. H. Grützmacher, Angew. Chem. 2008, 120, 1838-1842
176. Angew. Chem. Int. Ed. 2008, 47, 1814-1818
177. J. I. van der Vlugt, J. N. H. Reek, Angew. Chem. 2009, 121, 8990-9004
178. Angew. Chem. Int. Ed. 2009, 48, 8832-8846
179. T. Ikariya, I. D. Gridnev, Chem. Rec. 2009, 9, 106-123
180. K. Ishiwata, S. Kuwata, T. Ikariya, J. Am. Chem. Soc. 2009, 131, 5001-5009
181. S. Kuwata, T. Ikariya, Dalton Trans. 2010, 39, 2984-2992
182. M. Ito, C. Kobayashi, A. Himizu, T. Ikariya, J. Am. Chem. Soc. 2010, 132, 11414-11415
183. I. D. Gridnev, M. Watanabe, H. Wang, T. Ikariya, J. Am. Chem. Soc. 2010, 132, 16637-16650
184. T. Ikariya, I. D. Gridnev, Top. Catal. 2010, 53, 894-901
185. T. Ikariya, S. Kuwata, Y. Kayaki, Pure Appl. Chem. 2010, 82, 1471-1483
186. M. Ito, A. Shiibashi, T. Ikariya, Chem. Commun. 2011, 47, 2134-2136
187. T. Ikariya, Bull. Chem. Soc. Jpn. 2011, 84, 1-16
188. M. Ito, T. Ootsuka, R. Watari, A. Shiibashi, A. Himizu, T. Ikariya, J. Am. Chem. Soc. 2011, 133, 4240-4242
189. R. H. Crabtree, New J. Chem. 2011, 35, 18-23
190. T. Ikariya, Top. Organomet. Chem. 2011, 37, 31-53.
191. Z.-W. Li, T.-L. Wang, Y.-M. He, Z.-J. Wang, Q.-H. Fan, J. Pan, L.-J. Xu, Org. Lett. 2008, 10, 5265-5268.
192. S.-Y. Shirai, H. Nara, Y. Kayaki, T. Ikariya, Organometallics 2009, 28, 802-809.
193. C. Li, C. Wang, B. Villa-Marcos, J. Xiao, J. Am. Chem. Soc. 2008, 130, 14450-14451.
194. M. Rueping, R. M. Koenigs, Chem. Commun. 2011, 47, 304-306.
195. D.-W. Wang, W. Zeng, Y.-G. Zhou, Tetrahedron: Asymmetry 2007, 18, 1103-1107.
196. D.-W. Wang, D.-S. Wang, Q.-A. Chen, Y.-G. Zhou, Chem. Eur. J. 2010, 16, 1133-1136.
197. R. H. Morris, Chem. Soc. Rev. 2009, 38, 2282-2291.
198. S. Hashiguchi, A. Fujii, J. Takehara, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 7562-7563.
199. M. Kitamura, T. Ohkuma, S. Inoue, N. Sayo, H. Kumobayashi, S. Akutagawa, T. Ohta, H. Takaya, R. Noyori, J. Am. Chem. Soc. 1988, 110, 629-631.
200. T. Ohkuma, H. Ooka, S. Hashiguchi, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1995, 117, 2675-2676.
201. T. Ohkuma, M. Koizumi, H. Doucet, T. Pham, M. Kozawa, K. Murata, E. Katayama, T. Yokozawa, T. Ikariya, R. Noyori, J. Am. Chem. Soc. 1998, 120, 13529-13530
202. T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086
203. H. Doucet, T. Ohkuma, K. Murata, T. Yokozawa, M. Kozawa, E. Katayama, A. F. England, T. Ikariya, R. Noyori, Angew. Chem. 1998, 110, 1792-1796
204. Angew. Chem. Int. Ed. 1998, 37, 1703-1707
205. T. Ohkuma, C. A. Sandoval, R. Srinivasan, Q. Lin, Y. Wei, K. Muñiz, R. Noyori, J. Am. Chem. Soc. 2005, 127, 8288.
206. N. B. Johnson, I. C. Lennon, P. H. Moran, J. A. Ramsden, Acc. Chem. Res. 2007, 40, 1291-1299.
207. R. Noyori, Angew. Chem. 2002, 114, 2108-2123
208. Angew. Chem. Int. Ed. 2002, 41, 2008-2022.
209. D. S. Matharu, D. J. Morris, G. J. Clarkson, M. Wills, Chem. Commun. 2006, 3232-3234
210. D. J. Morris, A. M. Hayes, M. Wills, J. Org. Chem. 2006, 71, 7035-7044
211. D. S. Matharu, D. J. Morris, A. M. Kawamoto, G. J. Clarkson, M. Wills, Org. Lett. 2005, 7, 5489-5491
212. A. M. Hayes, D. J. Morris, G. J. Clarkson, M. Wills, J. Am. Chem. Soc. 2005, 127, 7318-7319
213. X. Wu, X. Li, F. King, J. Xiao, Angew. Chem. 2005, 117, 3473-3477
214. Angew. Chem. Int. Ed. 2005, 44, 3407-3411
215. P. N. Liu, P. M. Gu, F. Wang, Y. Q. Tu, Org. Lett. 2003, 5, 169-172
216. J. Hannedouche, G. J. Clarkson, M. Wills, J. Am. Chem. Soc. 2004, 126, 986-987
217. T. Hamada, T. Torii, K. Izawa, R. Noyori, T. Ikariya, Org. Lett. 2002, 4, 4373-4376
218. D. G. I. Petra, P. C. J. Kamer, P. W. N. M. van Leeuwen, K. Goubitz, A. M. Van Loon, J. G. de Vries, H. E. Schoemaker, Eur. J. Inorg. Chem. 1999, 2335-2341
219. M. Palmer, T. Walsgrove, M. Wills, J. Org. Chem. 1997, 62, 5226-5228; For examples of other efficient Ru and Rh catalyzed ATH, see
220. J. Wettergren, E. Buitrago, P. Ryberg, H. Adolfsson, Chem. Eur. J. 2009, 15, 5709-5718
221. W. Baratta, M. Bosco, G. Chelucci, A. Del Zotto, K. Siega, M. Toniutti, E. Zangrando, P. Rigo, Organometallics 2006, 25, 4611-4620
222. A. B. Zaitsev, H. Adolfsson, Org. Lett. 2006, 8, 5129-5132
223. M. T. Reetz, X. Li, J. Am. Chem. Soc. 2006, 128, 1044-1045
224. D. A. Alonso, D. Guijarro, P. Pinho, O. Temme, P. G. Andersson, J. Org. Chem. 1998, 63, 2749-2751
225. Y. Jiang, Q. Jiang, X. Zhang, J. Am. Chem. Soc. 1998, 120, 3817-3818
226. J.-X. Gao, H. Zhang, X.-D. Yi, P.-P. Xu, C.-L. Tang, H.-L. Wan, K.-R. Tsai, T. Ikariya, Chirality 2000, 12, 383-388
227. J.-X. Gao, T. Ikariya, R. Noyori, Organometallics 1996, 15, 1087-1089
228. T. Touge, T. Hakamata, H. Nara, T. Kobayashi, N. Sayo, T. Saito, Y. Kayaki, T. Ikariya, J. Am. Chem. Soc. 2011, 133, 14960-14963.
229. M. J. Burk, W. Hems, D. Herzberg, C. Malan, A. Zanotti-Gerosa, Org. Lett. 2000, 2, 4173-4176
230. J. Wu, H. Chen, W. Kwok, R. Guo, Z. Zhou, C. Yeung, A. S. C. Chan, J. Org. Chem. 2002, 67, 7908-7910
231. X. Li, W. Chen, W. Hems, F. King, J. Xiao, Org. Lett. 2003, 5, 4559-4561
232. J. Wu, J.-X. Ji, R. Guo, C.-H. Yeung, A. S. C. Chan, Chem. Eur. J. 2003, 9, 2963-2968
233. A. Hu, H. L. Ngo, W. Lin, Org. Lett. 2004, 6, 2937-2940
234. Y. Xu, N. W. Alcock, G. J. Clarkson, G. Docherty, G. Woodward, M. Wills, Org. Lett. 2004, 6, 4105-4107
235. Y. Xu, G. C. Clarkson, G. Docherty, C. L. North, G. Woodward, M. Wills, J. Org. Chem. 2005, 70, 8079-8087
236. S. Burk, G. Francio, W. Leitner, Chem. Commun. 2005, 3460-3462
237. Q. Jing, X. Zhang, J. Sun, K. Ding, Adv. Synth. Catal. 2005, 347, 1193-1197
238. M. Ito, Y. Endo, T. Ikariya, Organometallics 2008, 27, 6053-6055
239. T. Ohkuma, K. Tsutsumi, N. Utsumi, N. Arai, R. Noyori, K. Murata, Org. Lett. 2006, 8, 255-257
240. T. Ohkuma, N. Utsumi, K. Tsutsumi, K. Murata, C. Sandoval, R. Noyori, J. Am. Chem. Soc. 2006, 128, 8724-8725
241. H. Huang, T. Okuno, K. Tsuda, M. Yoshimura, M. Kitamura, J. Am. Chem. Soc. 2006, 128, 8716-8717
242. W. Li, X. Sun, L. Zhou, G. Hou, S. Yu, X. Zhang, J. Org. Chem. 2008, 73, 1397-1399
243. N. Arai, K. Suzuki, S. Sugizaki, H. Sorimachi, T. Ohkuma, Angew. Chem. 2008, 120, 1794-1797
244. Angew. Chem. Int. Ed. 2008, 47, 1770-1773
245. N. Arai, H. Ooka, K. Azuma, T. Yabuuchi, N. Kurono, T. Inoue, T. Ohkuma, Org. Lett. 2007, 9, 939-941
246. K. Mikami, K. Wakabayashi, K. Aikawa, Org. Lett. 2006, 8, 1517-1519
247. F. Naud, C. Malan, F. Spindler, C. Rüggeberg, A. T. Schmidt, H.-U. Blaser, Adv. Synth. Catal. 2006, 348, 47-50.
248. J. Trocha-Grimshaw, H. B. Henbest, J. Chem. Soc. Chem. Comm. 1967, 544-544.
249. G. Zassinovich, C. del Bianco, G. Mestroni, J. Organomet. Chem. 1981, 222, 323-329.
250. G. Zassinovich, G. Mestroni, J. Mol. Catal. 1987, 42, 81-90.
251. G. Zassinovich, R. Bettella, G. Mestroni, N. Bresciani-Pahor, S. Geremia, L. Randaccio, J. Organomet. Chem. 1989, 370, 187-202.
252. R. Spogliarich, G. Zassinovich, J. Kaspar, M. Graziani, J. Mol. Catal. 1982, 16, 359-361.
253. R. Spogliarich, J. Kaspar, M. Graziani, F. Morandini, J. Organomet. Chem. 1986, 306, 407-412.
254. P. Kvintovics, J. Bakos, B. Heil, J. Mol. Catal. 1985, 32, 111-114.
255. H. W. Krause, A. K. Bhatnagar, J. Organomet. Chem. 1986, 302, 265-267.
256. D. Müller, G. Umbricht, B. Weber, A. Pfaltz, Helv. Chim. Acta 1991, 74, 232-240.
257. N. Debono, M. L. Besson, C. Pinel, L. Djakovitch, Tetrahedron Lett. 2004, 45, 2235-2238
258. P. Paredes, J. Díez, M. P. Gamasa, Organometallics 2008, 27, 2597-2607
259. A. Trifonova, K. E. Källström, P. G. Andersson, Tetrahedron 2004, 60, 3393-3403.
260. R. ter Halle, A. Bréhéret, E. Schulz, C. Pinel, M. Lemaire, Tetrahedron: Asymmetry 1997, 8, 2101-2108.
261. R. ter Halle, E. Schulz, M. Lemaire, Synlett 1997, 1257-1258.
262. P. Gamez, B. Dunjic, M. Lemaire, J. Org. Chem. 1996, 61, 5196-5197.
263. P. Gamez, B. Dunjic, F. Fache, M. Lemaire, J. Chem. Soc. Chem. Commun. 1994, 1417-1418.
264. E. Breysse, C. Pinel, M. Lemaire, Tetrahedron: Asymmetry 1998, 9, 897-900.
265. S.-I. Inoue, K. Nomura, S. Hashiguchi, R. Noyori, Y. Izawa, Chem. Lett. 1997, 26, 957-958.
266. K. Murata, T. Ikariya, R. Noyori, J. Org. Chem. 1999, 64, 2186-2187.
267. K. Mashima, T. Abe, K. Tani, Chem. Lett. 1998, 27, 1199-1200.
268. K. Mashima, T. Abe, K. Tani, Chem. Lett. 1998, 27, 1201-1202.
269. T. Thorpe, J. Blacker, S. M. Brown, C. Bubert, J. Crosby, S. Fitzjohn, J. P. Muxworthy, J. M. J. Williams, Tetrahedron Lett. 2001, 42, 4041-4043.
270. X. Wu, D. Vinci, T. Ikariya, J. Xiao, Chem. Commun. 2005, 4447-4449.
271. X. Wu, X. Li, A. Zanotti-Gerosa, A. Pettman, J. Liu, A. J. Mills, J. Xiao, Chem. Eur. J. 2008, 14, 2209-2222.
272. F. Wang, H. Liu, L. Cun, J. Zhu, J. Deng, Y. Jiang, J. Org. Chem. 2005, 70, 9424-9429.
273. X. Li, J. Blacker, I. Houson, X. Wu, J. Xiao, Synlett 2006, 1155-1160.
274. O. Soltani, M. A. Ariger, H. Vázquez-Villa, E. M. Carreira, Org. Lett. 2010, 12, 2893-2895.
275. H. Vázquez-Villa, S. Reber, M. A. Ariger, E. M. Carreira, Angew. Chem. 2011, 123, 9141-9143
276. Angew. Chem. Int. Ed. 2011, 50, 8979-8981.
277. G. Liu, H. Gu, Y. Sun, J. Long, Y. Xu, H. Li, Adv. Synth. Catal. 2011, 353, 1317-1324.
278. K. Ahlford, H. Adolfsson, Catal. Commun. 2011, 12, 1118-1121.
279. A. Hartikka, S. A. Modin, P. G. Andersson, P. I. Arvidsson, Org. Biomol. Chem. 2003, 1, 2522-2526.
280. W. He, B.-L. Zhang, R. Jiang, P. Liu, X.-L. Sun, S.-Y. Zhang, Tetrahedron Lett. 2006, 47, 5367-5370.
281. W. He, P. Liu, B. Le Zhang, X. Li Sun, S. Y. Zhang, Appl. Organomet. Chem. 2006, 20, 328-334.
282. D. G. I. Petra, P. C. J. Kamer, A. L. Spek, H. E. Schoemaker, P. W. N. M. van Leeuwen, J. Org. Chem. 2000, 65, 3010-3017.
283. A. Hage, D. G. I. Petra, J. A. Field, D. Schipper, J. B. P. A. Wijnberg, P. C. J. Kamer, J. N. H. Reek, P. W. N. M. van Leeuwen, R. Wever, H. E. Schoemaker, Tetrahedron: Asymmetry 2001, 12, 1025-1034.
284. Y.-Y. Li, H. Zhang, J.-S. Chen, X.-L. Liao, Z.-R. Dong, J.-X. Gao, J. Mol. Catal. A 2004, 218, 153-156.
285. J.-S. Chen, Y.-Y. Li, Z.-R. Dong, B.-Z. Li, J.-X. Gao, Tetrahedron Lett. 2004, 45, 8415-8418.
286. Z.-R. Dong, Y.-Y. Li, J.-S. Chen, B.-Z. Li, Y. Xing, J.-X. Gao, Org. Lett. 2005, 7, 1043-1045.
287. B.-Z. Li, J.-S. Chen, Z.-R. Dong, Y.-Y. Li, Q.-B. Li, J.-X. Gao, J. Mol. Catal. A 2006, 258, 113-117.
288. Y. Xing, J.-S. Chen, Z.-R. Dong, Y.-Y. Li, J.-X. Gao, Tetrahedron Lett. 2006, 47, 4501-4503.
289. X.-Q. Zhang, Y.-Y. Li, H. Zhang, J.-X. Gao, Tetrahedron: Asymmetry 2007, 18, 2049-2054.
290. X.-Q. Zhang, Y.-Y. Li, Z.-R. Dong, W.-Y. Shen, Z.-B. Cheng, J.-X. Gao, J. Mol. Catal. A 2009, 307, 149-153.
291. G. Chen, Y. Xing, H. Zhang, J.-X. Gao, J. Mol. Catal. A 2007, 273, 284-288.
292. W.-Y. Shen, H. Zhang, H.-L. Zhang, J.-X. Gao, Tetrahedron: Asymmetry 2007, 18, 729-733.
293. R. J. Lundgren, M. Stradiotto, Chem. Eur. J. 2008, 14, 10388-10395.
294. R. Spogliarich, E. Farnetti, J. Kaŝpar, M. Graziani, E. Cesarotti, J. Mol. Catal. 1989, 50, 19-29.
295. E. Cesarotti, L. Prati, M. Pallavicini, L. Villa, R. Spogliarich, E. Farnetti, M. Graziani, J. Mol. Catal. 1990, 62, L29-L37.
296. X. Zhang, T. Taketomi, T. Yoshizumi, H. Kumobayashi, S. Akutagawa, K. Mashima, H. Takaya, J. Am. Chem. Soc. 1993, 115, 3318-3319.
297. E. Le Roux, R. Malacea, E. Manoury, R. Poli, L. Gonsalvi, M. Peruzzini, Adv. Synth. Catal. 2007, 349, 309-313.
298. L. Dahlenburg, R. Menzel, F. W. Heinemann, Eur. J. Inorg. Chem. 2007, 4364-4374.
299. L. Dahlenburg, D. Kramer, F. W. Heinemann, J. Coord. Chem. 2010, 63, 2673-2684.
300. K. Makino, Y. Hiroki, Y. Hamada, J. Am. Chem. Soc. 2005, 127, 5784-5785.
301. K. Makino, M. Iwasaki, Y. Hamada, Org. Lett. 2006, 8, 4573-4576.
302. T. Maeda, K. Makino, M. Iwasaki, Y. Hamada, Chem. Eur. J. 2010, 16, 11954-11962.
303. J.-B. Xie, J.-H. Xie, X.-Y. Liu, W.-L. Kong, S. Li, Q.-L. Zhou, J. Am. Chem. Soc. 2010, 132, 4538-4539.
304. J.-B. Xie, J.-H. Xie, X.-Y. Liu, Q.-Q. Zhang, Q.-L. Zhou, Chem. Asian J. 2011, 6, 899-908.
305. J.-H. Xie, X.-Y. Liu, J.-B. Xie, L.-X. Wang, Q.-L. Zhou, Angew. Chem. 2011, 123, 7467-7470
306. Angew. Chem. Int. Ed. 2011, 50, 7329-7332.
307. J.-H. Xie, X.-Y. Liu, X.-H. Yang, J.-B. Xie, L.-X. Wang, Q.-L. Zhou, Angew. Chem. 2012, 124, 205-207
308. Angew. Chem. Int. Ed. 2012, 51, 201-203.
309. M. L. Tommasino, C. C. Thomazeau, F. O. Touchard, M. Lemaire, Tetrahedron: Asymmetry 1999, 10, 1813-1819.
310. A. Ferrand, M. Bruno, M. L. Tommasino, M. Lemaire, Tetrahedron: Asymmetry 2002, 13, 1379-1384.
311. C. L. Maillet, T. Praveen, P. Janvier, S. B. Minguet, M. Evain, C. Saluzzo, M. L. Tommasino, B. Bujoli, J. Org. Chem. 2002, 67, 8191-8196.
312. J. E. D. Martins, D. J. Morris, M. Wills, Tetrahedron Lett. 2009, 50, 688-692.
313. J. E. D. Martins, M. Wills, Tetrahedron 2009, 65, 5782-5786.
314. Z. M. Heiden, T. B. Rauchfuss, J. Am. Chem. Soc. 2009, 131, 3593-3600.
315. T. Ohkuma, N. Utsumi, M. Watanabe, K. Tsutsumi, N. Arai, K. Murata, Org. Lett. 2007, 9, 2565-2567.
316. M. Ito, Y. Endo, N. Tejima, T. Ikariya, Organometallics 2010, 29, 2397-2399.
317. G. Liu, M. Yao, J. Wang, X. Lu, M. Liu, F. Zhang, H. Li, Adv. Synth. Catal. 2008, 350, 1464-1468.
318. G. Liu, J. Wang, T. Huang, X. Liang, Y. Zhang, H. Li, J. Mater. Chem. 2010, 20, 1970-1975.
319. H.-Y. Jiang, C.-F. Yang, C. Li, H.-Y. Fu, H. Chen, R.-X. Li, X.-J. Li, Angew. Chem. 2008, 120, 9380-9384
320. Angew. Chem. Int. Ed. 2008, 47, 9240-9244.
321. T. Irrgang, D. Friedrich, R. Kempe, Angew. Chem. 2008, 120, 2231-2234
322. Angew. Chem. Int. Ed. 2011, 50, 2183-2186.
323. For a review on iridium-catalyzed oxidation of alcohols, see:, T. Suzuki, Chem. Rev. 2011, 111, 1825-1845.
324. N. Ahlsten, B. Martín-Matute, Chem. Commun. 2011, 47, 8331-8333
325. I. Cumpstey, S. Agrawal, E. K. Borbas, B. Martín-Matute, Chem. Commun. 2011, 47, 7827-7829
326. N. Ahlsten, A. Bartoszewicz, S. Agrawal, B. Martín-Matute, Synthesis 2011, 2600-2608
327. A. Bartoszewicz, R. Marcos, S. Sahoo, A. K. Inge, X. Zou, B. Martín-Matute, Chem. Eur. J. 2012, 18, 14510-14519
328. N. Ahlsten, A. Bermejo Gomez, B. Martín-Matute, Angew. Chem. 2013, DOI: 10.1002/ange.201301013;
329. Angew. Chem. Int. Ed. 2013, DOI: 10.1002/anie.201301013.
330. Z. Yuecheng, Z. Shanshan, M. Guorui, Z. Jiquan, Prog. Chem. 2012, 24, 212-224.
331. E. M. Ferreira, B. M. Stoltz, J. Am. Chem. Soc. 2001, 123, 7725-7726
332. D. R. Jensen, J. S. Pugsley, M. S. Sigman, J. Am. Chem. Soc. 2001, 123, 7475-7476
333. W. Sun, H. Wang, C. Xia, J. Li, P. Zhao, Angew. Chem. 2003, 115, 1072-1074
334. Angew. Chem. Int. Ed. 2003, 42, 1042-1044
335. M. S. Sigman, D. R. Jensen, Acc. Chem. Res. 2006, 39, 221-229
336. Z. Li, Z. H. Tang, X. X. Hu, C. G. Xia, Chem. Eur. J. 2005, 11, 1210-1216
337. Y.-Y. Li, X.-Q. Zhang, Z.-R. Dong, W.-Y. Shen, G. Chen, J.-X. Gao, Org. Lett. 2006, 8, 5565-5567
338. S. Sahoo, P. Kumar, F. Lefebvre, S. B. Halligudi, Appl. Catal. A 2009, 354, 17-25
339. T. Kunisu, T. Oguma, T. Katsuki, J. Am. Chem. Soc. 2011, 133, 12937-12939
340. D. Xu, S. Wang, Z. Shen, C. Xia, W. Sun, Org. Biomol. Chem. 2012, 10, 2730-2732.
341. J. Zhang, X. Yang, H. Zhou, Y. Li, Z. J. Gao, Green Chem. 2012, 14, 1289-1292.
342. S. Arita, T. Koike, Y. Kayaki, T. Ikariya, Angew. Chem. 2008, 120, 2481-2483
343. Angew. Chem. Int. Ed. 2008, 47, 2447-2449.
344. B. M. Stoltz, Chem. Lett. 2004, 33, 362-367.
345. T. Suzuki, K. Ghozati, T. Katoh, H. Sasai, Org. Lett. 2009, 11, 4286-4288
346. T. Suzuki, K. Ghozati, D.-Y. Zhou, T. Katoh, H. Sasai, Tetrahedron 2010, 66, 7562-7568
347. T. Suzuki, K. Morita, Y. Matsuo, K. Hiroi, Tetrahedron Lett. 2003, 44, 2003-2006.
348. J. M. Keith, J. F. Larrow, E. N. Jacobsen, Adv. Synth. Catal. 2001, 343, 5-26
349. D. E. J. E. Robinson, S. D. Bull, Tetrahedron: Asymmetry 2003, 14, 1407-1446
350. E. Vedejs, M. Jure, Angew. Chem. 2005, 117, 4040-4069
351. Angew. Chem. Int. Ed. 2005, 44, 3974-4001
352. A. Ghanem, H. Y. Aboul-Enein, Chirality 2005, 17, 1-15
353. J. R. Dehli, V. Gotor, Chem. Soc. Rev. 2002, 31, 365-370.
354. R. S. Ward, Tetrahedron: Asymmetry 1995, 6, 1475-1490
355. F. F. Huerta, A. B. E. Minidis, J.-E. Backvall, Chem. Soc. Rev. 2001, 30, 321-331
356. H. Pellissier, Tetrahedron 2003, 59, 8291-8327
357. H. Pellissier, Tetrahedron 2008, 64, 1563-1601
358. R. Marcos, B. Martín-Matute, Isr. J. Chem. 2012, 52, 639-652.
359. R. Stürmer, Angew. Chem. 1997, 109, 1221-1222
360. Angew. Chem. Int. Ed. Engl. 1997, 36, 1173-1174
361. O. Pàmies, J.-E. Bäckvall, Chem. Rev. 2003, 103, 3247-3262
362. M.-J. Kim, Y. Ahn, J. Park, Bull. Korean Chem. Soc. 2005, 26, 515-522
363. Y. Ahn, S.-B. Ko, M.-J. Kim, J. Park, Coord. Chem. Rev. 2008, 252, 647-658
364. B. Martín-Matute, J.-E. Bäckvall, Curr. Opin. Chem. Biol. 2007, 11, 226-232
365. A. Kamal, M. A. Azhar, T. Krishnaji, M. S. Malik, S. Azeeza, Coord. Chem. Rev. 2008, 252, 569-592
366. A. H. Kamaruddin, M. H. Uzir, H. Y. Aboul-Enein, H. N. A. Halim, Chirality 2009, 21, 449-467
367. J. H. Lee, K. Han, M.-J. Kim, J. Park, Eur. J. Org. Chem. 2010, 2010, 999-1015
368. N. J. Turner, Curr. Opin. Chem. Biol. 2010, 14, 115-121
369. Y. Kim, J. Park, M.-J. Kim, ChemCatChem 2011, 3, 271-277
370. H. Pellissier, Tetrahedron 2011, 67, 3769-3802.
371. M. Stirling, J. Blacker, M. I. Page, Tetrahedron Lett. 2007, 48, 1247-1250.
372. A. J. Blacker, M. J. Stirling, M. I. Page, Org. Process Res. Dev. 2007, 11, 642-648.
373. A. C. Marr, C. L. Pollock, G. C. Saunders, Organometallics 2007, 26, 3283-3285.
374. Y. Sato, Y. Kayaki, T. Ikariya, Chem. Commun. 2012, 48, 3635-3637.
375. R. M. Haak, F. Berthiol, T. Jerphagnon, A. J. A. Gayet, C. Tarabiono, C. P. Postema, V. Ritleng, M. Pfeffer, D. B. Janssen, A. J. Minnaard, B. L. Feringa, J. G. de Vries, J. Am. Chem. Soc. 2008, 130, 13508-13509
376. T. Jerphagnon, J. A. Gayet Arnaud, F. Berthiol, V. Ritleng, N. Mrsic, A. Meetsma, M. Pfeffer, J. Minnaard Adriaan, L. Feringa Ben, G. de Vries Johannes, Chem. Eur. J. 2009, 15, 12780-12790.
377. For Ru-catalyzed DKR of β-chloroalcohols, see:, A. Träff, K. Bogár, M. Warner, J.-E. Bäckvall, Org. Lett. 2008, 10, 4807-4810.