Cinchonas and Cupreidines

Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications

Volumn 1-3, Issue , 2013, Pages 117-160

  Ingemann, Steen ^a   Hiemstra, Henk ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

C9 amines; C9 esters; C9 ethers; Phase transfer catalysis; Thiourea derivatives

Indexed keywords

AMINES;

PHASE TRANSFER CATALYSIS; THIOUREA DERIVATIVES;

CATALYSIS;

EID: 85008868497     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527658862.ch6     Document Type: Chapter

References (177)

1. Kaufman, T.S. and Rúveda, E.A. (2005) Angew. Chem. Int. Ed., 44, 854-885.
2. Song, C.E. (ed.) (2009) Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis, Wiley-VCH Verlag GmbH, Weinheim.
3. Dalko, P.I. and Moisan, L. (2004) Angew. Chem. Int. Ed., 43, 5138-5175.
4. Marcelli, T., van Maarseveen, J.H., and Hiemstra, H. (2006) Angew. Chem. Int. Ed., 45, 7496-7504.
5. Dalko, P.I. (ed.) (2007) Enantioselective Organocatalysis: Reactions and Experimental Procedures, Wiley-VCH Verlag GmbH, Weinheim.
6. Dondoni, A. and Massi, A. (2008) Angew. Chem. Int. Ed., 47, 4638-4660.
7. Connon, S.J. (2008) Chem. Commun., 2499-2510.
8. Bertelsen, S. and Jørgensen, K.A. (2009) Chem. Soc. Rev., 38, 2178-2189.
9. Marcelli, T. and Hiemstra, H. (2010) Synthesis, 1229-1279.
10. Li, H., Chen, Y., and Deng, L. (2011) in Privileged Chiral Ligands and Catalysts (ed. Q.-L. Zhou), Wiley-VCH Verlag GmbH, Weinheim, ch. 10, pp. 361-408.
11. Yeboah, E.M.O., Yeboah, S.O., and Singh, G.S. (2011) Tetrahedron, 67, 1725-1762.
12. Bhanushali, M. and Zhao, C.-G. (2011) Synthesis, 1815-1830.
13. Nielsen, M., Worgull, D., Zweifel, T., Gschwend, B., Bertelsen, S., and Jørgensen, K.A. (2011) Chem. Commun., 632-649.
14. Blaser, H.-U. (2009) in Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis (ed. C.E. Song), Wiley-VCH Verlag GmbH, Weinheim, ch. 2, pp. 13-128.
15. Kacprak, K. and Gawronski, J. (2009) in Cinchona Alkaloids in Synthesis and Catalysis: Ligands, Immobilization and Organocatalysis (ed. C.E. Song), Wiley-VCH Verlag GmbH, Weinheim, ch. 13, pp. 421-469.
16. Bredig, G. and Fiske, P.S. (1912) Biochem. Z., 46, 7.
17. Pracejus, H. (1960) Justus Liebigs Ann. Chem., 634, 9-22.
18. Wynberg, H. (1986) Top. Stereochem., 16, 87-129.
19. Hiemstra, H. and Wynberg, H. (1981) J. Am. Chem. Soc., 103, 417-430.
20. O' Donnell, M.J. (2004) Acc. Chem. Res., 37, 506-517.
21. Lygo, B. and Andrews, B.I. (2004) Acc. Chem. Res., 37, 518-525.
22. Sharpless, K.B. (1994) Chem. Rev., 94, 2483-2547.
23. Corey, E.J. and Noe, M.C. (1996) J. Am. Chem. Soc., 118, 319-329.
24. Vayner, G., Houk, K.N., and Sun, Y.-K. (2004) J. Am. Chem. Soc., 126, 199-203.
25. Dijkstra, G.D.H., Kellogg, R.M., and Wynberg, H. (1989) Recl. Trav. Chim. Pays-Bas, 108, 95.
26. Dijkstra, G.D.H., Kellogg, R.M., Wynberg, H.J.S., Svendsen, Marko, I., and Sharpless, K.B. (1989) J. Am. Chem. Soc., 111, 8069-8076.
27. Dijkstra, G.D.H., Kellogg, R.M., and Wynberg, H. (1990) J. Org. Chem., 55, 6121-6131.
28. Bürgi, T. and Baiker, A. (1998) J. Am. Chem. Soc., 120, 12920-12926.
29. Olsen, R.A., Borchardt, D., Mink, L.y., Agarwal, A., Mueller, L.J., and Zaera, F. (2011) J. Am. Chem. Soc., 133, 9992-9995.
30. Surya Prakash, G.K., Wang, F., Ni, C., Shen, J., Haiges, R., Yudin, A.K., Mathew, T., and Olah, G.A. (2011) J. Am. Chem. Soc., 133, 9992-9995.
31. Kumar, A., Salunkhe, R.V., Rane, R.A., and Dike, S.Y. (1991) J. Chem. Soc., Chem. Commun., 485-486.
32. Tanaka, T., Kumamoto, T., and Ishikawa, T. (2000) Tetrahedron: Asymmetry, 11, 4633-4637.
33. Sekino, E., Kumamoto, T., Tanaka, T., Ikeda, T., and Ishikawa, T. (2004) J. Org. Chem., 69, 2760-2767.
34. Bartoli, G., Bosco, M., Carlone, A., Cavalli, A., Locatelli, M., Mazzanti, A., Ricca, P., Sambri, L., and Melchiorre, P. (2006) Angew. Chem. Int. Ed., 45, 4966-4970.
35. Wang, H.-F., Zheng, C.-W., Yang, Y.-Q., Chai, Z., and Zhao, G. (2008) Tetrahedron: Asymmetry, 19, 2608-2615.
36. Sun, W., Ma, X., Hong, L., and Wang, R. (2011) J. Org. Chem., 76, 7826-7833.
37. Capuzzi, M., Perdicchia, D., and Jørgensen, K.A. (2008) Chem. Eur. J., 14, 128-135.
38. Nakamura, S., Hayashi, M., Hiramatsu, Y., Shibata, N., Funahashi, Y., and Toru, T. (2009) J. Am. Chem. Soc., 131, 18240-18241.
39. Russo, A. and Lattanzi, A. (2010) Eur. J. Org. Chem., 6736-6673.
40. Li, H., Wang, Y., Tang, L., and Deng, L. (2004) J. Am. Chem. Soc., 126, 9906-9907.
41. Dodda, R., Goldman, J.J., Mandal, T., Zhao, C.-G., Broker, G.A., and Tiekink, E.R.T. (2008) Adv. Synth. Catal., 350, 537-541.
42. Liu, L., Zhang, S., Xue, F., Lou, G., Zhang, H., Ma, S., Duan, W., and Wang, W. (2011) Chem. Eur. J., 17, 7791-7795.
43. Deng, J., Zhang, S., Ding, P., Jiang, H., Wang, W., and Li, J. (2010) Adv. Synth. Catal., 352, 833-838.
44. Chen, W.-B., Wu, Z.-J., Pei, Q.-L., Cun, L.-F., Zhang, X.-M., and Yuan, W.-C. (2010) Org. Lett., 12, 3132-3135.
45. Nakano, A., Ushiyama, M., Iwabuchi, Y., and Hatakeyama, S. (2005) Adv. Synth. Catal., 347, 1790-1796.
46. Hoffmann, H.M.R. and Frackenpohl, J. (2004) Eur. J. Org. Chem., 4293-4312.
47. Iwabuchi, Y., Nakatani, M., Yokoyama, N., and Hatakeyama, S. (1999) J. Am. Chem. Soc., 121, 10219-10220.
48. Nakano, A., Kawahara, S., Akamatsu, S., Morokuma, K., Nakatani, M., Iwabuchi, Y., Takahashi, K., Ishihara, J., and Hatakeyama, S. (2006) Tetrahedron, 62, 381-389.
49. Nakano, A., Takahashi, K., Ishihara, J., and Hatakeyama, S. (2005) Heterocycles, 66, 371-383.
50. Kanano, A., Ushiyama, M., Iwabuchi, Y., and Hatakeyama, S. (2005) Adv. Synth. Catal., 347, 1790-1796.
51. Li, H., Wang, Y., Tang, L., Wu, F., Liu, X., Guo, C., Foxman, B.M., and Deng, L. (2005) Angew. Chem. Int. Ed., 44, 105-108.
52. Papageorgiou, C.D., Ley, S.V., and Gaunt, M.J. (2003) Angew. Chem. Int. Ed., 42, 828-831.
53. Papageorgiou, C.D., Cubillo de Dios, M.A., Ley, S.V., and Gaunt, M.J. (2004) Angew. Chem. Int. Ed., 43, 4641-4644.
54. Johansson, C.C.C., Bremeyer, N., Ley, S.V., Owen, D.R., Smith, S.C., and Gaunt, M.J. (2006) Angew. Chem. Int. Ed., 45, 6024-6028.
55. Wang, X., Fong, T., and Tong, X. (2011) Angew. Chem. Int. Ed., 50, 5361-5364.
56. Ishii, Y., Fujimoto, R., Mikami, M., Murakami, S., Miki, Y., and Furukawa, Y. (2007) Org. Process Res. Dev., 11, 609-615.
57. Xiao, X., Xi, Y., Su, C., Liu, M., and Shi, Y. (2011) J. Am. Chem. Soc., 133, 12914-12917.
58. He, P., Liu, X., Shi, J., Lin, L., and Feng, X. (2011) Org. Lett., 13, 936-939.
59. Wu, F., Li, H., Hong, R., and Deng, L. (2006) Angew. Chem. Int. Ed., 45, 947-950.
60. Wu, F., Hong, R., Khan, J., Liu, X., and Deng, L. (2006) Angew. Chem. Int. Ed., 45, 4301-4305.
61. Wang, Y., Liu, X., and Deng, L. (2006) J. Am. Chem. Soc., 128, 3928-3930.
62. Rigby, C.L. and Dixon, D.J. (2008) Chem. Commun, 3798-3800.
63. Kawahara, S., Nakano, A., Esumi, T., Iwabuchi, Y., and Hatakeyama, S. (2003) Org. Lett., 5, 3103-3105.
64. Hatakeyama, S. (2006) J. Synth. Org. Chem. Jpn., 64, 1132-1138.
65. Nakano, A., Takahashi, K., Ishihara, J., and Hatakeyama, S. (2006) Org. Lett., 8, 5357-5360.
66. van Steenis, D.J.V.C., Marcelli, T., Lutz, M., Spek, A.L., van Maarseveen, J.H., and Hiemstra, H. (2007) Adv. Synth. Catal., 349, 281-286.
67. Sarkar, S.M., Wanzala, E.N., Shibahara, S., Takahashi, K., Ishihara, J., and Hatakeyama, S. (2009) Chem. Commun., 5907-5909.
68. Shi, M., Qi, M.-J., and Liu, X.-G. (2008) Chem. Commun., 6025-6027.
69. Liu, Y.-L., Wang, B.-L., Cao, J.-J., Chen, L., Zhang, Y.-X., Wang, C., and Zhou, J. (2010) J. Am. Chem. Soc., 132, 15176-15178.
70. Zhong, F., Chen, G.-Y., and Lu, Y. (2011) Org. Lett., 13, 82-85.
71. Saaby, S., Bella, M., and Jørgensen, K.A. (2004) J. Am. Chem. Soc., 126, 8120-8121.
72. Dückert, H., Khedkar, V., Waldmann, H., and Kumar, K. (2011) Chem. Eur. J., 17, 5130-5137.
73. Zhao, M.-X., Zhang, Z.-W., Chen, M.-X., Tang, W.-H., and Shi, M. (2011) Eur. J. Org. Chem., 3001-3008.
74. Bekele, T., Shah, M.H., Wolfer, J., Abraham, C.J., Weatherwax, A., and Lectka, T. (2006) J. Am. Chem. Soc., 128, 1810-1811.
75. Wolfer, J., Bekele, T., Abraham, C.J., Dogo-Isonagie, C., and Lectka, T. (2006) Angew. Chem. Int. Ed., 45, 7398-7400.
76. Li, H., Wang, B., and Deng, L. (2006) J. Am. Chem. Soc., 128, 732-733.
77. Shi, M., Lei, Z.-Y., Zhao, M.-X., and Shi, J.-W. (2007) Tetrahedron Lett., 48, 5743-5746.
78. Bandini, M., Sinisi, R., and Umani-Ronchi, A. (2008) Chem. Commun., 4360-4362.
79. Chauhan, P. and Chimni, S.S. (2011) Eur. J. Org. Chem., 1636-1640.
80. Malerich, J.P., Hagihara, K., and Rawal, V.H. (2008) J. Am. Chem. Soc., 130, 14416-14417.
81. Konishi, H., Lam, T.Y., Malerich, J.P., and Rawal, V.T. (2010) Org. Lett., 12, 2028-2031.
82. Zhu, Y., Malerich, J.P., and Rawal, V.H. (2010) Angew. Chem. Int. Ed., 49, 153-156.
83. Nakanishi, W. (2009) in Superbases for Organic Synthesis (ed. T. Ishikawa), John Wiley & Sons, Ltd, Chichester, ch. 9, pp. 273-294.
84. Bordwell, F.G. and Ji, G.-Z. (1991) J. Am. Chem. Soc., 113, 8398-8401.
85. Li, X., Deng, H., Zhang, B., Li, J., Zhang, L., Luo, S., and Cheng, J.-P. (2010) Chem. Eur. J., 16, 450-455.
86. Sigman, M.S. and Jacobsen, E.N. (1998) J. Am. Chem. Soc., 120, 4901-4902.
87. Okino, T., Hoashi, Y., and Takemoto, Y. (2003) J. Am. Chem. Soc., 125, 12672-12673.
88. Li, B.-J., Jiang, L., Liu, M., Chen, Y.-C., Ding, L.-S., and Wu, Y. (2005) Synlett, 604-606.
89. Ye, J., Dixon, D.J., and Hynes, P.S. (2005) Chem. Commun., 4481-4483.
90. Vakulya, B., Varga, S., Csámpai, A., and Soós, T. (2005) Org. Lett., 7, 1967-1969.
91. Vakulya, B., Varga, S., and Soós, T. (2008) J. Org. Chem., 73, 3475-3480.
92. McCooey, S.H. and Connon, S.J. (2005) Angew. Chem. Int. Ed., 44, 6367-6370.
93. Marcelli, T., Van der Haas, R.N.S., Van Maarseveen, J.H., and Hiemstra, H. (2006) Angew. Chem. Int. Ed., 45, 929-931.
94. Hammar, P., Marcelli, T., Hiemstra, H., and Himo, F. (2007) Adv. Synth. Catal., 349, 2537-2548.
95. Xie, H., Zhang, Y., Zhang, S., Chen, X., and Wang, W. (2011) Angew. Chem. Int. Ed., 50, 11773-11776.
96. Zhao, Q.-Y., Pei, C.-K., Guan, X.-Y., and Shi, M. (2011) Adv. Synth. Catal., 353, 1973-1979.
97. Zhang, Y., Shao, Y.-L., Xu, H.-S., and Wang, W. (2011) J. Org. Chem., 76, 1472-1474.
98. Li, P., Chan, S.H., Chan, A.S.C., and Kwong, F.Y. (2011) Org. Biomol. Chem., 9, 7997-7999.
99. Li, X.-J., Peng, F.-Z., Li, X., Wu, W.-T., Sun, Z.-W., Li, Y.-M., Zhang, S.-X., and Shao, Z.-H. (2011) Chem. Asian J., 6, 220-225.
100. Wu, B., Liu, G.-G., Li, M.-Q., Zhang, Y., Zhang, S.-Y., Qui, J.-R., Xu, X.-P., Ji, S.-J., and Wang, X.-W. (2011) Chem. Commun., 3992-3994.
101. Bai, S., Ling, X., Song, B., Bhadury, P.S., Hu, D., and Yang, S. (2011) Tetrahedron: Asymmetry, 22, 518-523.
102. Li, L., Song, B., Bhadury, P.S., Zhang, Y.-P., Hu, D.-Y., and Yang, S. (2011) Eur. J. Org. Chem., 4743-4746.
103. Liu, Y., Sun, B., Wang, B., Wakem, M., and Deng, L. (2009) J. Am. Chem. Soc., 131, 418-419.
104. Breman, A.C., Smits, J.M.M., de Gelder, R., van Maarseveen, J.H., Ingemann, S., and Hiemstra, H. (2012) Synlett, 23, 2195-2200.
105. Oh, S.H., Rho, H.S., Lee, J.W., Youk, S.H., Chin, J., and Song, C.E. (2008) Angew. Chem. Int. Ed., 47, 7872-7875.
106. Tárkányi, G., Király, P., Varga, S., Vakulya, B., and Soós, T. (2008) Chem. Eur. J., 14, 6078-6086.
107. Rho, H.S., Oh, S.H., Lee, J.W., Lee, J.Y., Chin, J., and Song, C.E. (2008) Chem. Commun., 1208-1210.
108. Jang, H.B., Rho, H.S., Oh, J.S., Nam, E.H.B., Park, S.E., Bae, H.Y., and Song, C.E. (2008) Org. Biomol. Chem., 8, 3918-3922.
109. Xiong, F., Chen, X.-X., and Chen, F.-E. (2010) Tetrahedron: Asymmetry, 21, 665-669.
110. Park, S.E., Nam, E.H., Jang, H.B., Oh, J.S., Some, S., Lee, Y.S., and Song, C.E. (2010) Adv. Synth. Catal., 352, 2211-2217.
111. Luo, J., Xu, L.-W., and Hay, R.A.S. (2009) Org. Lett., 11, 437-440.
112. Yang, W. and Du, D.-M. (2010) Org. Lett., 12, 5450-5453.
113. Dai, L., Wang, S.-X., and Chen, F.-E. (2010) Adv. Synth. Catal., 352, 2137-2141.
114. Bae, H.Y., Some, S., Oh, J.S., Lee, Y.S., and Song, C.E. (2011) Chem. Commun., 47, 9621-9623.
115. Bae, H.Y., Some, S., Lee, J.H., Kim, J.-Y., Song, M.J., Lee, S., Zhang, Y.J., and Song, C.E. (2011) Adv. Synth. Catal., 353, 3196-3202.
116. Xu, D.-Q., Wang, Y.-F., Zhang, W., Luo, S.-P., Zhong, A.-G., Xia, A.-B., and Xu, Z.-Y. (2010) Chem. Eur. J., 16, 4177-4180.
117. Lee, J.W., Ryu, T.H., Oh, J.S., Bae, H.Y., Bin Jang, H., and Song, C.E. (2009) Chem. Commun., 7224-7226.
118. Han, X., Zhong, F., and Lu, Y. (2010) Adv. Synth. Catal., 352, 2778-2782.
119. Zhang, L., Lee, M.-M., Lee, S.-M., Lee, J., Cheng, M., Jeong, B.-S., Park, H., and Jew, S. (2009) Adv. Synth. Catal., 351, 3063-3066.
120. Lee, M., Zhang, L., Park, Y., and Park, H. (2012) Tetrahedron, 68, 1452-1459.
121. Chen, Y.-C. (2008) Synlett, 1919-1930.
122. Jiang, L. and Chen, Y.-C. (2011) Catal. Sci. Technol., 1, 354-365.
123. Brunne, H., Bügler, J., and Nuber, B. (1995) Tetrahedron: Asymmetry, 6, 1699-1702.
124. Mukherjee S., Yang, J.W., Hoffmann, S., and List, B. (2007) Chem. Rev., 107, 5471-5569.
125. Melchiorre, P., Marigo, M., Carlone, A., and Bartoli, G. (2008) Angew. Chem. Int. Ed., 47, 6138-6171.
126. Vicario, J.L., Badía, D., Carrillo, L., and Reyes, E. (2010) Organocatalytic Enantioselective Conjugate Addition Reactions: A Powerful Tool for the Stereocontrolled Synthesis of Complex Molecules, RSC Publishing, Cambridge.
127. McCooey, S.H. and Connon, S.J. (2007) Org. Lett., 9, 599-602.
128. Xie, J.-W., Chen, W., Li, R., Zeng, M., Du, W., Yue, L., Chen, Y.-C., Wu, Y., Zhu, J., and Deng, J.-G. (2007) Angew. Chem. Int. Ed., 46, 389-392.
129. Chen, W., Du, W., Yeu, L., Li, R., Wu, Y., Ding, L.-S., and Chen, Y.-C. (2007) Org. Biomol. Chem., 5, 816-821.
130. Bartoli, G., Bosco, M., Carlone, A., Pesciaioli, F., Sambri, L., and Melchiorre, P. (2007) Org. Lett., 9, 1403-1405.
131. Ricci, P., Carlone, A., Bartoli, G., Bosco, M., Sambri, L., and Melchiorre, P. (2008) Adv. Synth. Catal., 350, 49-53.
132. Zhang, E., Fen, C.-A., Tu, Y.-Q., Zhang, F.-M., and Song, Y.-L. (2009) J. Am. Chem. Soc., 131, 14626-14627.
133. Zheng, B.-L., Liu, Q.-Z., Guo, C.-S., Wang, X.-L., and He, L. (2007) Org. Biomol. Chem., 5, 2913-2915.
134. Liu, C., Dou, X., and Li, Y. (2011) Org. Lett., 13, 5248-5251.
135. A. Lee, A. Michrowska, S. Sulzer-Mosse, and B. List (2011) Angew. Chem. Int. Ed., 50, 1707-1710.
136. List, B. (2010) Angew. Chem. Int. Ed., 49, 1730-1734.
137. Cai, Q., Zheng, C., Zhang, J.-W., and You, S.-L. (2011) Angew. Chem. Int. Ed., 50, 8665-8669.
138. Czarnecki, P., Plutecka, A., Grawronski, J., and Kacprzak, K. (2011) Green Chem., 13, 1280-1287.
139. Zhou, J., Wakchaure, V., Kraft, P., and List, B. (2008) Angew. Chem. Int. Ed., 47, 7656-7658.
140. Denmark, S.E., Gould, N.D., and Wolff, L.M. (2011) J. Org. Chem., 76, 4260-4336.
141. Denmark, S.E., Gould, N.D., and Wolff, L.M. (2011) J. Org. Chem., 76, 4337-4357.
142. Denmark, S.E. and Weinstraub, R.C. (2011) Heterocycles, 82, 1527-1540.
143. Jew, S.-S. and Park, H.-G. (2009) Chem. Commun., 7090-7103.
144. Dolling, U.-H., Davis, P., and Grabowski, E.J.J. (1984) J. Am. Chem. Soc., 106, 446-447.
145. Bhattacharya, A., Dolling, U.-H., Grabowski, E.J.J., Karady, S., Ryan, K.M., and Weinstock, L.M. (1986) Angew. Chem. Int. Ed., 25, 476-477.
146. Hughes, D.L., Dolling, U.-H., Ryan, K.M., Schoenewaldt, E.F., and Grabowski, E.J.J. (1987) J. Org. Chem., 52, 4745-4752.
147. O' Donnell, M.J., Bennett, W.D., and Wu, S. (1989) J. Am. Chem. Soc., 111, 2353-2355.
148. O' Donnell, M.J., Bennett, W.D., Bruder, W.A., Jacobsen, W.N., Knuth, K., LeClef, B., Pelt, R.L., Bordwell, F.G., Mrozack, S.R., and Cripe, T.A. (1988) J. Am. Chem. Soc., 110, 8520-8525.
149. Lygo, B. and Wainwright, P.G. (1997) Tetrahedron Lett., 38, 8595-8598.
150. Lygo, B., Crosby, J., Lowdon, T.R., and Wainwright, P.G. (2011) Tetrahedron, 57, 2391-2402.
151. Corey, E.J., Xu, F., and Noe, M.C. (1997) J. Am. Chem. Soc., 119, 12414 - 12415.
152. Corey, E.J., Bo, Y., and Busch-Petersen, J. (1998) J. Am. Chem. Soc., 120, 13000-13001.
153. Jew, S.-S., Lee, J.-H., Jeong, B.-S., Yoo, M.-S., Kim, M.-J., Lee, Y.-J., Lee, J., Choi, S.-H., Lee, K., Lah, M.S., and Park, H.-G. (2005) Angew. Chem. Int. Ed., 44, 1383-1385.
154. Tarí, S., Chincilla, R., and Najera, C. (2010) Tetrahedron: Asymmetry, 21, 2872-2878.
155. Wei, Y., He, W., Liu, Y., Liu, P., and Zhang, S. (2012) Org. Lett., 14, 704-707.
156. Li, F., Li, Y.-Z., Jia, Z.-S., Xu, M.-H., Tian, P., and Lin, G.-Q. (2011) Tetrahedron, 67, 10186-10194.
157. Choi, D.S., Han, S.S., Kwueon, E.K., Choi, H.Y., Hwang, S.H., Park, Y.S., and Song, C.E. (2006) Adv. Synth. Catal., 348, 2560-2564.
158. Claraz, A., Leroy, J., Oudeyer, S., and Levacher, V. (2011) J. Org. Chem., 76, 6457-6443.
159. Lozano, O., Blessley, G., Martinez del Campo, T., Thompson, A.L., Giuffredi, G.T., Bettati, M., Walker, M., Borman, R., and Gouverneur, V. (2011) Angew. Chem. Int. Ed., 50, 8105-8109.
160. Chen, Z.-M., Zhang, Q.-W., Chen, Z.-H., Li, H., Tu, Y.-Q., Zhang, F.-M., and Tian, J.-M. (2011) J. Am. Chem. Soc., 133, 8818-8821.
161. Li, H., Zhang, F.-M., Tu, Y.-Q., Zhang, Q.-W., Chen, Z.-M., Chen, Z.-H., and Li, J. (2011) Chem. Sci., 2, 1839-1841.
162. Furukawa, T., Nishimine, T., Tokunaga, E., Hasegawa, K., Shiro, M., and Shibata, N. (2011) Org. Lett., 13, 3972-3975.
163. Companó, X., Valero, G., Ceban, V., Calvet, T., Font-Bardía, M., Moyano, A., and Rios, R. (2011) Org. Biomol. Chem., 9, 7986-7989.
164. Cui, H.-L., Sun, X.-H., Jiang, L., Dong, L., and Chen, Y.-C. (2011) Eur. J. Org. Chem., 7366-7371.
165. Jiang, L., Lei, Q., Huang, X., Cui, H.-L., Zhou, X., and Chen, Y.-C. (2011) Chem. Eur. J., 17, 9489-9493.
166. Wu, Y., Singh, R.P., and Deng, L. (2011) J. Am. Chem. Soc., 133, 12458-12461.
167. Abermil, N., Masson, G., and Zhu, J. (2008) J. Am. Chem. Soc., 130, 12596-12597.
168. Li, W., Wu, W., Yu, F., Huang, H., Liang, X., and Ye, J. (2011) Org. Biomol. Chem., 9, 2505-2511.
169. Zhao, M.-X., Tang, W.-H., Chen, M.-X., Wei, D.-K., Dai, T.-L., and Shi, M. (2011) Eur. J. Org. Chem., 6078-6084.
170. Chen, J.-R., Cao, Y.-J., Zou, Y.-Q., Tan, F., Fu, L., Zhu, X.-Y., and Xiao, W.-J. (2010) Org. Biomol. Chem., 8, 1275-1279.
171. Chen, J.-R., Zou, Y.-Q., Fu, L., Ren, F., Tan, F., and Xiao, W.-J. (2010) Tetrahedron, 66, 5367-5372.
172. Lu, L.-Q., An, X.-L., Chen, J.-R., and Xiao, W.-J. (2012) Synlett, 490-508.
173. Palacio, C. and Connon, S.J. (2011) Org. Lett., 13, 1298-1301.
174. Palacio, C. and Connon, S.J. (2012) Chem. Commun., 2849-2851.
175. Boraty n ski, P.J., Turowska-Tyrk, I., and Skar z ewski, J. (2008) Org. Lett., 10, 385-388.
176. Quigley, C., Rodriques-Docampo, Z., and Connon, S.J. (2012) Chem. Commun., 1443-1445.
177. Rodrígues-Docampo, Z., Quigley, C., Tallon, S., and Connon, S.J. (2012) J. Org. Chem., 77, 2407-2414.