Recent developments in asymmetric aziridination

Advanced Synthesis and Catalysis

Volumn 356, Issue 9, 2014, Pages 1899-1935

  Pellissier, Hélène ^a  

^a AIX MARSEILLE UNIVERSITÉ   (France)

Author keywords

asymmetric catalysis; asymmetric synthesis; aziridines; chirality; enantioselectivity; strained molecules

Indexed keywords

EID: 84902537537     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400312     Document Type: Review

References (233)

1. S. Gabriel, Ber. dtsch. chem. Ges. 1888, 21, 1049-1057
2. S. Gabriel, Ber. dtsch. chem. Ges. 1888, 21, 2664-2669.
3. A. Padwa, in: Comprehensive Heterocyclic Chemistry III, (Eds.:, A. Ramsden, E. F. V. Scriven, R. J. K. Taylor,), Elsevier, Oxford, 2008, chap. 1, pp 1-104
4. T. Beck Bisol, M. Mandolesi Sà, Quim. Nova 2007, 30, 106-115
5. G. S. Singh, M. D'hooghe, N. De Kimpe, Chem. Rev. 2007, 107, 2080-2135
6. J. B. Sweeney, in: Aziridines and Epoxides in Organic Synthesis, (Ed.:, A. Yudin,), Wiley-VCH, Weinheim, 2006, chap. 4, pp 117-144
7. V. K. Aggarwal, M. Badine, V. Moorthie, in: Aziridines and Epoxides in Organic Synthesis, (Ed.:, A. Yudin,), Wiley-VCH, Weinheim, 2006, chap. 1, pp 1-35
8. P. Zhou, B.-C. Chen, F. A. Davis, in: Aziridines and Epoxides in Organic Synthesis, (Ed.:, A. Yudin,), Wiley-VCH, Weinheim, 2006, chap. 3, pp 73-115
9. A. Padwa, S. S. Murphree, Arkivoc 2006, iii, 6-33
10. G. Cardillo, L. Gentilucci, A. Tolomelli, Aldrichimica Acta 2003, 36, 39-50
11. W. K. Lee, H.-J. Ha, Aldrichimica Acta 2003, 36, 57-63
12. A. Padwa, S. Murphree, Progress in Heterocyclic Chemistry, (Eds.:, G. W. Gribble, T. L. Gilchrist,), Elsevier Science. Oxford, 2000, Vol. 15, pp 75- 99
13. A. Padwa, S. S. Murphree, in: Progress in Heterocyclic Chemistry, (Eds.:, G. W. Gribble, T. L. Gilchrist,), Elsevier Science. Oxford, 2000, Vol. 12, Chap. 4.1, p 57
14. A. Padwa, W. H. Pearson, B. N. Lian, S. C. Bergmeier, in: Comprehensive Heterocyclic Chemistry II, (Eds.:, A. R. Katritzky, C. W. Reese, E. F. Scriven,), Pergamon, Oxford, 1996, Vol. 1 A, p 1
15. J. E. G. Kemp, in: Comprehensive Organic Synthesis, (Eds.:, B. M. Trost, I. Fleming,), Pergamon, Oxford, 1991, Vol. 7, Chap. 3.5, p 469
16. A. Padwa, A. D. Woolhouse, in: Comprehensive Heterocyclic Chemistry, (Ed.:, W. Lwowski,), Pergamon Press, Oxford, 1984, Vol. 7, pp 47- 93.
17. T. Tanner, Pure Appl. Chem. 1993, 65, 1319-1328
18. D. Tanner, Angew. Chem. 1994, 106, 625-646
19. Angew. Chem. Int. Ed. Engl. 1994, 33, 599-619
20. R. S. Atkinson, Tetrahedron 1999, 55, 1519-1559
21. A. Yudin, in: Aziridines and Epoxides in Organic Synthesis, Wiley-VCH, Weinheim, 2006
22. H. Stamm, J. Prakt. Chem. 1999, 341, 319-331
23. W. McCoull, F. A. Davis, Synthesis 2000, 1347-1365
24. A. Padwa, in: Comprehensive Organic Synthesis, (Eds.:, B. M. Trost, I. Fleming,), Pergamon, Oxford, 1991, Vol. 4, Chap. 4.9, p 1069
25. G. Righi, C. Bonini, Targets Heterocycl. Syst. 2000, 4, 139-165
26. B. Zwanenburg, P. ten Holte, Stereoselective Heterocyclic Synthesis III, (Ed.:, P. Metz,), in: Topics in Current Chemistry, Springer, Berlin, 2001, Vol. 216, pp 93- 124
27. J. B. Sweeney, Chem. Soc. Rev. 2002, 31, 247-258
28. J. Aires-de-Sousa, S. Prabhakar, A. M. Lobo, A. M. Rosa, M. J. S. Gomes, M. C. Corvo, D. J. Williams, A. J. P. White, Tetrahedron: Asymmetry 2002, 12, 3349-3365
29. X. E. Hu, Tetrahedron 2004, 60, 2701-2743
30. M. Pineschi, Eur. J. Org. Chem. 2006, 4979-4988
31. S. Florio, R. Luisi, Chem. Rev. 2010, 110, 5128-5157
32. P. Lu, Tetrahedron 2010, 66, 2549-2560.
33. I. A. Zalialov, V. H. Dahanubar, Curr. Opin. Drug Discovery Dev. 2002, 5, 918-927.
34. H. Pellissier, Tetrahedron 2010, 66, 1509-1555.
35. H. M. I. Osborn, J. B. Sweeney, Tetrahedron: Asymmetry 1997, 8, 1693-1715
36. P. Müller, C. Fruit, Chem. Rev. 2003, 103, 2905-2919
37. C. Mössner, C. Bolm, in: Transition Metals for Organic Synthesis, 2 nd edn., (Eds.:, M. Beller, C. Bolm,), Wiley-VCH, Weinheim, 2004, pp 389-402.
38. V. K. Aggarwal, E. M. McGarrigle, M. A. Shaw, Science of Synthesis, Georg Thieme Verlag, Stuttgart, 2010, Vol. 37, pp 311- 347
39. H. Muchalski, J. N. Johnston, Science of Synthesis, Georg Thieme Verlag, Stuttgart, 2011, Vol. 1, pp 155- 184
40. D. Karila, R. H. Dodd, Curr. Org. Chem. 2011, 15, 1509-1540
41. J. W. W. Chang, T. M. U. Ton, P. W. H. Chan, Chem. Rec. 2011, 11, 331-357
42. N. Jung, S. Bräse, Angew. Chem. 2012, 124, 5632-5634
43. Angew. Chem. Int. Ed. 2012, 51, 5538-5540
44. R. Chawla, A. K. Singh, L. D. S. Yadav, RSC Adv. 2013, 3, 11385-11403
45. P.-A. Wang, Beilstein J. Org. Chem. 2013, 9, 1677-1695.
46. F. A. Davis, P. Zhou, C.-H. Liang, R. E. Reddy, Tetrahedron: Asymmetry 1995, 6, 1511-1514
47. J. L. Garcia Ruano, I. Fernandez, C. Hamdouchi, Tetrahedron Lett. 1995, 36, 295-298
48. J. L. Garcia Ruano, I. Fernandez, M. del Prado Catalina, A. A. Cruz, Tetrahedron: Asymmetry 1996, 7, 3407-3414.
49. A.-H. Li, L.-X. Dai, V. K. Aggarwal, Chem. Rev. 1997, 97, 2341-2372
50. L.-X. Dai, X.-L. Hou, Y.-G. Zhou, Pure Appl. Chem. 1999, 71, 369-376.
51. D. Morton, R. A. Stockman, Tetrahedron 2006, 62, 8869-8905.
52. Z. Xue, V. M. Dee, L. J. Hope-Weeks, B. R. Whittlesey, M. F. Mayer, Arkivoc 2010, vii, 65-80.
53. R. Robiette, J. Org. Chem. 2006, 71, 2726-2734
54. V. K. Aggarwal, J. P. H. Charmant, C. Ciampi, J. M. Hornby, C. J. O'Brien, G. Hynd, R. Parsons, J. Chem. Soc. Perkin Trans. 1 2001, 3159-3166.
55. Fluoroorganic Chemistry. Synthetic Challenge and Biomedicinal Rewards, Vol. 58, (Eds.: G. Resnati, V. A. Soloshonok), Tetrahedron 1996, 52, 1-300.
56. Y. Yang, Y. Huang, F.-L. Qing, Tetrahedron Lett. 2013, 54, 3826-3830.
57. O. Illa, M. Arshad, A. Ros, E. M. McGarrigle, V. K. Aggarwal, J. Am. Chem. Soc. 2010, 132, 1828-1830.
58. O. Illa, M. Namutebi, C. Saha, M. Ostovar, C. C. Chen, M. F. Haddow, S. Nocquet-Thibault, M. Lusi, E. M. McGarrigle, V. K. Aggarwal, J. Am. Chem. Soc. 2013, 135, 11951-11966.
59. I. Dokli, I. Matanovic, Z. Hamersak, Chem. Eur. J. 2010, 16, 11744-11752.
60. S. A. Kavanagh, A. Piccinini, S. J. Connon, Org. Biomol. Chem. 2013, 11, 3535-3540.
61. W. Kirmse, in: Carbene Chemistry, 2 nd edn., McGraw-Hill, New York, 1971, p 412
62. F. Badea, C. Condeiu, M. Gherghiu, A. Iancu, A. Iordache, C. Simion, Rev. Roum. Chim. 1992, 37, 393-405.
63. T. Hashimoto, H. Nakatsu, S. Watanabe, K. Maruoka, Org. Lett. 2010, 12, 1668-1671.
64. T. Hashimoto, H. Nakatsu, K. Yamamoto, S. Watanabe, K. Maruoka, Chem. Asian J. 2011, 6, 607-613.
65. Y. Arroyo, A. Meana, M. A. Sanz-Tejedor, I. Alonso, J. L. Garcia Ruano, Chem. Eur. J. 2010, 16, 9874-9883.
66. F. Colpaert, S. Mangelinckx, S. De Brabandere, N. De Kimpe, J. Org. Chem. 2011, 76, 2204-2213.
67. G. Callebaut, S. Mangelinckx, L. Kiss, R. Sillanpää, F. Fülöp, N. De Kimpe, Org. Biomol. Chem. 2012, 10, 2326-2338.
68. G. Callebaut, S. Mangelinckx, P. Van der Veken, K. W. Törnroos, K. Augustyns, N. De Kimpe, Beilstein J. Org. Chem. 2012, 8, 2124-2131.
69. M. K. Ghorai, K. Ghosh, A. K. Yadav, Y. Nanaji, S. Halder, M. Sayyad, J. Org. Chem. 2013, 78, 2311-2326.
70. T. M. Solà, I. Churcher, W. Lewis, R. A. Stockman, Org. Biomol. Chem. 2011, 9, 5034-5035.
71. P. V. Kattamuri, Y. Xiong, Y. Pan, G. Li, Org. Biomol. Chem. 2013, 11, 3400-3408.
72. F. Colpaert, S. Mangelinckx, E. Leemans, B. Denolf, N. De Kimpe, Org. Biomol. Chem. 2010, 8, 3251-3258.
73. H. Suzuki, S. Aoyagi, Org. Lett. 2012, 14, 6374-6376.
74. W.-J. Liu, Y.-H. Zhao, X.-W. Sun, Tetrahedron Lett. 2013, 54, 3586-3590.
75. O. Pablo, D. Guijarro, M. Yus, J. Org. Chem. 2013, 78, 9181-9189.
76. T. Ishikawa, K. Hada, T. Watanabe, T. Isobe, J. Am. Chem. Soc. 2001, 123, 7707-7708.
77. T. Haga, T. Ishikawa, Tetrahedron 2005, 61, 2857-2869
78. T. Ishikawa, Arkivoc 2006, vii, 148-168.
79. W. Disadee, T. Ishikawa, J. Org. Chem. 2005, 70, 9399-9406.
80. I. Khantikaew, M. Takahashi, T. Kumamoto, N. Suzuki, T. Ishikawa, Tetrahedron 2012, 68, 878-882.
81. T. Kumamoto, K. Suzuki, S.-k. Kim, K. Hoshino, M. Takahashi, H. Sato, H. Iwata, K. Ueno, M. Fukuzumi, T. Ishikawa, Helv. Chim. Acta 2010, 93, 2109-2113.
82. A. S. Konev, K. A. Tehrani, A. F. Khlebnikov, M. S. Novikov, J. Magull, Russ. J. Org. Chem. 2010, 46, 976-986.
83. T. Uchida, T. Katsuki, Chem. Rec. 2014, 14, 117-129.
84. P. Dauban, R. H. Dodd, Synlett 2003, 1571-1586.
85. T. Katsuki, Chem. Lett. 2005, 34, 1304-1309.
86. D. A. Evans, M. M. Faul, M. T. Bilodeau, B. A. Anderson, D. M. Barnes, J. Am. Chem. Soc. 1993, 115, 5328-5329
87. Z. Li, K. R. Conser, E. N. Jacobsen, J. Am. Chem. Soc. 1993, 115, 5326-5327.
88. B. M. Trost, T. Zhang, Chem. Eur. J. 2011, 17, 3630-3643.
89. V. D. B. Bonifacio, C. Gonzalez-Bello, H. S. Rzepa, S. Prabhakar, A. M. Lobo, Synlett 2010, 145-149.
90. F. Grellepois, J. Nonnenmacher, F. Lachaud, C. Portella, Org. Biomol. Chem. 2011, 9, 1160-1168.
91. T. Katagiri, Y. Katayama, M. Taeda, T. Ohshima, N. Iguchi, J. Org. Chem. 2011, 76, 9305-9311.
92. P.-Y. Géant, J. Martinez, L. Rocard, X. J. Salom-Roig, Synthesis 2012, 44, 1247-1252.
93. L.-D. Nie, F.-F. Wang, W. Ding, X.-X. Shi, X. Lu, Tetrahedron: Asymmetry 2013, 24, 638-642.
94. S. G. Davies, A. M. Fletcher, A. B. Frost, J. A. Lee, P. M. Roberts, Tetrahedron 2013, 69, 8885-8898.
95. A. Koohang, J. L. Bailey, R. M. Coates, H. K. Erickson, D. Owen, C. D. Poulter, J. Org. Chem. 2010, 75, 4769-4777.
96. C. Molinaro, A.-A. Guilbault, B. Kosjek, Org. Lett. 2010, 12, 3772-3775.
97. H.-S. Chong, Y. Chen, Org. Lett. 2013, 15, 5912-5915.
98. D. Huang, X. Liu, L. Li, Y. Cai, W. Liu, Y. Shi, J. Am. Chem. Soc. 2013, 135, 8101-8104.
99. E. N. Jacobsen, in: Comprehensive Asymmetric Catalysis, Vol. II, (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, 1999, chap. 17, p 607
100. T. Katsuki, in: Comprehensive Coordination Chemistry II, Vol. 9. (Ed.:, J. McCleverty,), Elsevier Science, Oxford, 2003, chap. 9.4, p 207.
101. J. Egloff, M. Ranocchiari, A. Schira, C. Schotes, A. Mezzetti, Organometallics 2013, 32, 4690-4701.
102. Z. Lu, Y. Zhang, W. D. Wulff, J. Am. Chem. Soc. 2007, 129, 7185-7194
103. Y. Zhang, A. Desai, Z. Lu, G. Hu, Z. Ding, W. D. Wulff, Chem. Eur. J. 2008, 14, 3785-3803
104. A. P. Patwardhan, V. R. Pulgam, Y. Zhang, W. D. Wulff, Angew. Chem. 2005, 117, 6325-6328
105. Angew. Chem. Int. Ed. 2005, 44, 6169-6172
106. Y. Zhang, Z. Lu, A. Desai, W. D. Wulff, Org. Lett. 2008, 10, 5429-5432
107. S. Yu, C. Rabalakos, W. D. Mitchell, W. D. Wulff, Org. Lett. 2005, 7, 367-369.
108. A. A. Desai, R. Moran-Ramallal, W. D. Wulff, Org. Synth. 2011, 88, 224-237.
109. M. Mukherjee, A. K. Gupta, Z. Lu, Y. Zhang, W. D. Wulff, J. Org. Chem. 2010, 75, 5643-5660.
110. G. Hu, A. K. Gupta, R. H. Huang, M. Mukherjee, W. D. Wulff, J. Am. Chem. Soc. 2010, 132, 14669-14675.
111. A. A. Desai, H. Ren, M. Mukherjee, W. D. Wulff, Org. Process Res. Dev. 2011, 15, 1108-1115.
112. M. J. Vetticatt, A. A. Desai, W. D. Wulff, J. Org. Chem. 2013, 78, 5142-5152.
113. L. Huang, Y. Zhang, R. J. Staples, R. H. Huang, W. D. Wulff, Chem. Eur. J. 2012, 18, 5302-5313.
114. Z. Wang, F. Li, L. Zhao, Q. He, F. Chen, C. Zheng, Tetrahedron 2011, 67, 9199-9203.
115. Y. Deng, Y. R. Lee, C. A. Newman, W. D. Wulff, Eur. J. Org. Chem. 2007, 2068-2071.
116. A. A. Desai, W. D. Wulff, J. Am. Chem. Soc. 2010, 132, 13100-13103.
117. M. J. Vetticatt, A. A. Desai, W. D. Wulff, J. Am. Chem. Soc. 2010, 132, 13104-13107.
118. L. Huang, W. D. Wulff, J. Am. Chem. Soc. 2011, 133, 8892-8895.
119. T. Hashimoto, A. O. Galvez, K. Maruoka, J. Am. Chem. Soc. 2013, 135, 17667-17670.
120. I. Ugi, R. Meyr, U. Fetzer, C. Steinbrückner, Angew. Chem. 1959, 71, 386-388
121. R. V. A. Orru, M. de Greef, Synthesis 2003, 1471-1499.
122. L. F. Tietze, A. Modi, Med. Res. Rev. 2000, 20, 304-322
123. Multicomponent Reactions, (Eds.:, J. Zhu, H. Bienaymé,), Wiley-VCH, Weinheim, 2005
124. D. J. Ramõn, M. Yus, Angew. Chem. 2005, 117, 1628-1661
125. Angew. Chem. Int. Ed. 2005, 44, 1602-1634
126. G. Guillena, D. J. Ramon, M. Yus, Tetrahedron: Asymmetry 2007, 18, 693-700
127. Synthesis of Heterocycles via Multicomponent Reactions, (Eds.:, R. V. A. Orru, E. Ruijter,), in: Topics in Heterocyclic Chemistry, Vols. I and II, Springer, Berlin, 2010.
128. G. H. Posner, Chem. Rev. 1986, 86, 831-844
129. L. F. Tietze, U. Beifuss, Angew. Chem. 1993, 105, 137-170
130. Angew. Chem. Int. Ed. Engl. 1993, 32, 131-163
131. L. F. Tietze, Chem. Rev. 1996, 96, 115-136
132. L. F. Tietze, G. Brasche, K. Gericke, Domino Reactions in Organic Synthesis, Wiley-VCH, Weinheim, 2006
133. H. Pellissier, Tetrahedron 2006, 62, 2143-2173
134. H. Pellissier, Tetrahedron 2006, 62, 1619-1665
135. D. Enders, C. Grondal, M. R. M. Hüttl, Angew. Chem. 2007, 119, 1590-1601
136. Angew. Chem. Int. Ed. 2007, 46, 1570-1581
137. D. M. D'Souza, T. J. J. Müller, Chem. Soc. Rev. 2007, 36, 1095-1108
138. A.-N. Alba, X. Companyo, M. Viciano, R. Rios, Curr. Org. Chem. 2009, 13, 1432-1474
139. Chem. Soc. Rev. 38, 2009 (special issue on rapid formation of molecular complexity in organic synthesis)
140. M. Ruiz, P. Lopez-Alvarado, G. Giorgi, J. C. Menéndez, Chem. Soc. Rev. 2011, 40, 3445-3454
141. L. Albrecht, H. Jiang, K. A. Jørgensen, Angew. Chem. 2011, 123, 8642-8660
142. Angew. Chem. Int. Ed. 2011, 50, 8492-8509
143. H. Pellissier, Adv. Synth. Catal. 2012, 354, 237-294
144. C. De Graaff, E. Ruijter, R. V. A. Orru, Chem. Soc. Rev. 2012, 41, 3969-4009
145. H. Pellissier, Chem. Rev. 2013, 113, 442-524.
146. Z. Zhang, J. C. Antilla, Angew. Chem. 2012, 124, 11948-11952
147. Angew. Chem. Int. Ed. 2012, 51, 11778-11782
148. C. Vaxelaire, P. Winter, M. Christmann, Angew. Chem. 2011, 123, 3685-3687
149. Angew. Chem. Int. Ed. 2011, 50, 3605-3607
150. K. C. Nicolaou, J. S. Chen, Chem. Soc. Rev. 2009, 38, 2993-3009
151. B. B. Touré, D. G. Hall, Chem. Rev. 2009, 109, 4439-4486
152. M. Colombo, I. Peretto, Drug Discovery Today 2008, 13, 677-684
153. C. Hulme, V. Gore, Curr. Med. Chem. 2003, 10, 51-80
154. A. Padwa, S. K. Bur, Tetrahedron 2007, 63, 5341-5378.
155. H. Ren, W. D. Wulff, Org. Lett. 2010, 12, 4908-4911.
156. A. K. Gupta, M. Mukherjee, W. D. Wulff, Org. Lett. 2011, 13, 5866-5869.
157. A. K. Gupta, M. Mukherjee, G. Hu, W. D. Wulff, J. Org. Chem. 2012, 77, 7932-7944.
158. M. Mukherjee, Y. Zhou, A. K. Gupta, Y. Guan, W. D. Wulff, Eur. J. Org. Chem. 2014, 7, 1386-1390.
159. L. Huang, W. Zhao, R. J. Staples, W. D. Wulff, Chem. Sci. 2013, 4, 622-628.
160. H. Pellissier, Tetrahedron 2007, 63, 9267-9331
161. E. M. McGarrigle, E. L. Myers, O. Illa, M. A. Shaw, S. L. Riches, V. K. Aggarwal, Chem. Rev. 2007, 107, 5841-5883.
162. T. Hashimoto, N. Uchiyama, K. Maruoka, J. Am. Chem. Soc. 2008, 130, 14380-14381.
163. T. Hashimoto, H. Nakatsu, K. Yamamoto, K. Maruoka, J. Am. Chem. Soc. 2011, 133, 9730-9733.
164. Z. Chai, J.-P. Bouillon, D. Cahard, Chem. Commun. 2012, 48, 9471-9473.
165. Y. Gui, S. Shen, H.-Y. Wang, Z.-Y. Li, Z.-Z. Huang, Chem. Lett. 2007, 36, 1436-1437.
166. M.-T. Huang, H.-Y. Wu, R.-J. Chein, Chem. Commun. 2014, 50, 1101-1103.
167. O. O. Fadeyi, M. L. Schulte, C. W. Lindsley, Org. Lett. 2010, 12, 3276-3278.
168. N. Halland, A. Braunton, S. Bachmann, M. Marigo, K. A. Jørgensen, J. Am. Chem. Soc. 2004, 126, 4790-4791.
169. Y. Hayashi, T. Urushima, D. Sakamoto, K. Torii, H. Ishikawa, Chem. Eur. J. 2011, 17, 11715-11718.
170. S. E. Larson, G. Li, G. B. Rowland, D. Junge, R. Huang, H. L. Woodcock, J. C. Antilla, Org. Lett. 2011, 13, 2188-2191.
171. J. Vesely, I. Ibrahem, G.-L. Zhao, R. Rios, A. Cordova, Angew. Chem. 2007, 119, 792-795
172. Angew. Chem. Int. Ed. 2007, 46, 778-781.
173. H. Arai, N. Sugaya, N. Sasaki, K. Makino, S. Lectard, Y. Hamada, Tetrahedron Lett. 2009, 50, 3329-3332.
174. F. Pesciaioli, F. De Vincentiis, P. Galzerano, G. Bencivenni, G. Bartoli, A. Mazzanti, P. Melchiorre, Angew. Chem. 2008, 120, 8831-8834
175. Angew. Chem. Int. Ed. 2008, 47, 8703-8706.
176. L. Deiana, P. Dziedzic, G.-L. Zhao, J. Vesely, I. Ibrahem, R. Rios, J. Sun, A. Cordova, Chem. Eur. J. 2011, 17, 7904-7917.
177. A. Desmarchelier, D. Pereira de Sant'Ana, V. Terrasson, J. M. Campagne, X. Moreau, C. Greck, R. M. de Figueiredo, Eur. J. Org. Chem. 2011, 4046-4052
178. A. Desmarchelier, V. Coeffard, X. Moreau, C. Greck, Chem. Eur. J. 2012, 18, 13222-13225.
179. H. Jiang, K. S. Halskov, T. K. Johansen, K. A. Jørgensen, Chem. Eur. J. 2011, 17, 3842-3846.
180. K. S. Halskov, T. Naicker, M. E. Jensen, K. A. Jørgensen, Chem. Commun. 2013, 49, 6382-6384.
181. L. Albrecht, H. Jiang, G. Dickmeiss, B. Gschwend, S. G. Hansen, K. A. Jørgensen, J. Am. Chem. Soc. 2010, 132, 9188-9196
182. L. Albrecht, L. K. Ransborg, B. Gschwend, K. A. Jørgensen, J. Am. Chem. Soc. 2010, 132, 17886-17893
183. L. Albrecht, A. Albrecht, L. K. Ransborg, K. A. Jørgensen, Chem. Sci. 2011, 2, 1273-1277
184. L. Albrecht, L. K. Ransborg, A. Albrecht, L. Lykke, K. A. Jørgensen, Chem. Eur. J. 2011, 17, 13240-13246.
185. I. G. Molnar, E.-M. Tanzer, C. Daniliuc, R. Gilmour, Chem. Eur. J. 2014, 20, 794-800.
186. S. Fioravanti, M. G. Mascia, L. Pellacani, P. A. Tardella, Tetrahedron 2004, 60, 8073-8077.
187. F. De Vincentiis, G. Bencivenni, F. Pesciaioli, A. Mazzanti, G. Bartoli, P. Galzerano, P. Melchiorre, Chem. Asian J. 2010, 5, 1652-1656.
188. Y. Menjo, A. Hamajima, N. Sasaki, Y. Hamada, Org. Lett. 2011, 13, 5744-5747.
189. Y. Murakami, Y. Takeda, S. Minakata, J. Org. Chem. 2011, 76, 6277-6285.
190. A. Armstrong, R. D. C. Pullin, C. R. Jenner, K. Foo, A. J. P. White, Tetrahedron: Asymmetry 2014, 25, 74-86.
191. C. De Fusco, T. Fuoco, G. Croce, A. Lattanzi, Org. Lett. 2012, 14, 4078-4081.
192. P. C. B. Page, C. Bordogna, I. Strutt, Y. Chan, B. R. Buckley, Synlett 2013, 24, 2067-2072.
193. D. Worgull, G. Dickmeiss, K. L. Jensen, P. T. Franke, N. Holub, K. A. Jørgensen, Chem. Eur. J. 2011, 17, 4076-4080.
194. Z. Li, R. W. Quan, E. N. Jacobsen, J. Am. Chem. Soc. 1995, 117, 5889-5890.
195. A. Pfaltz, Acc. Chem. Res. 1993, 26, 339-345
196. A. K. Ghosh, P. Mathivanan, J. Cappiello, Tetrahedron: Asymmetry 1998, 9, 1-45
197. H. A. McManus, P. J. Guiry, Chem. Rev. 2004, 104, 4151-4202
198. G. Desimoni, G. Faita, K. A. Jørgensen, Chem. Rev. 2006, 106, 3561-3651.
199. D. A. Evans, K. A. Woerpel, M. M. Hinman, M. M. Faul, J. Am. Chem. Soc. 1991, 113, 726-728.
200. H. Lebel, M. Parmentier, Pure Appl. Chem. 2010, 82, 1827-1833.
201. H. Lebel, M. Parmentier, O. Leogane, K. Ross, C. Spitz, Tetrahedron 2012, 68, 3396-3409.
202. Y. Gök, T. Noël, J. Van der Eycken, Tetrahedron: Asymmetry 2010, 21, 2275-2280.
203. G. Malik, A. Estéoule, P. Retailleau, P. Dauban, J. Org. Chem. 2011, 76, 7438-7448.
204. S. Hajra, D. Sinha, J. Org. Chem. 2011, 76, 7334-7340.
205. S. Hajra, S. Bar, Chem. Commun. 2011, 47, 3981-3982.
206. S. Hajra, S. Bar, Tetrahedron: Asymmetry 2011, 22, 775-779.
207. S. Hajra, S. Bar, Tetrahedron: Asymmetry 2012, 23, 151-156.
208. J. E. Aaseng, S. Melnes, G. Reian, O. R. Gautun, Tetrahedron 2010, 66, 9790-9797.
209. K. Omura, M. Murakami, T. Uchida, R. Irie, T. Katsuki, Chem. Lett. 2003, 32, 354-355
210. T. Uchida, Y. Tamura, M. Ohba, T. Katsuki, Tetrahedron Lett. 2003, 44, 7965-7968
211. K. Omura, T. Uchida, R. Irie, T. Katsuki, Chem. Commun. 2004, 2060-2061
212. H. Kawabata, K. Omura, T. Katsuki, Tetrahedron Lett. 2006, 47, 1571-1574
213. H. Kawabata, K. Omura, T. Uchida, T. Katsuki, Chem. Asian J. 2007, 2, 248-256.
214. C. Kim, T. Uchida, T. Katsuki, Chem. Commun. 2012, 48, 7188-7190.
215. Y. Kukunaga, T. Uchida, Y. Ito, K. Matsumoto, T. Katsuki, Org. Lett. 2012, 14, 4658-4661.
216. J. E. Jones, J. V. Ruppel, G.-Y. Gao, T. M. Moore, X. P. Zhang, J. Org. Chem. 2008, 73, 7260-7265.
217. L.-M. Jin, X. Xu, H. Lu, X. Cui, L. Wojtas, X. P. Zhang, Angew. Chem. Int. Ed. 2013, 52, 5309-5313.
218. H. U. Blaser, E. Schmidt, in: Asymmetric Catalysis on Industrial Scale, Wiley-VCH, Weinheim, 2004.
219. H. B. Kagan, J. C. Fiaud, Top. Stereochem. 1988, 18, 249-330
220. A. H. Hoveyda, M. T. Didiuk, Curr. Org. Chem. 1998, 2, 489-526
221. G. R. Cook, Curr. Org. Chem. 2000, 4, 869-885
222. M. Keith, J. F. Larrow, E. N. Jacobsen, Adv. Synth. Catal. 2001, 343, 5-26
223. D. E. J. E. Robinson, S. D. Bull, Tetrahedron: Asymmetry 2003, 14, 1407-1446
224. E. Vedejs, M. Jure, Angew. Chem. 2005, 117, 4040-4069
225. Angew. Chem. Int. Ed. 2005, 44, 3974-4001
226. E. R. Jarvo, S. J. Miller, in: Comprehensive Asymmetric Catalysis, Supplement, (Eds.:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Berlin, 2004, pp 189-206.
227. H. Pellissier, Adv. Synth. Catal. 2011, 353, 1613-1666.
228. G. Bredig, K. Fajans, Ber. dtsch. chem. Ges. 1908, 41, 752-763
229. K. Fajans, Z. Phys. Chem. 1910, 73, 25-96.
230. K. Ohmatsu, Y. Hamajima, T. Ooi, J. Am. Chem. Soc. 2012, 134, 8794-8797.
231. J. Cockrell, C. Wilhelmsen, H. Rubin, A. Martin, J. B. Morgan, Angew. Chem. 2012, 124, 9980-9983
232. Angew. Chem. Int. Ed. 2012, 51, 9842-9845.
233. R. Moran-Ramallal, R. Liz, V. Gotor, J. Org. Chem. 2010, 75, 6614-6624.