参考文献
|
-
[1] J. Zhou, V. Wakchaure, P. Kraft, B. List, Angew. Chem. Int. Ed. 2008, 47, 7656-7658.
連結:
-
[2] P. Kraft, G. Frater, Chirality 2001, 13, 388-394.
連結:
-
[3] C. S. Sell, Chem Biodivers 2004, 1, 1899-1920.
連結:
-
[5] Nobelprize.org, The Nobel Prize in Chemistry 2001.
連結:
-
[6] H. G. Albrecht Berkessel, Asymmetric Organocatalysis: From Biomimetic Concepts to Applications in Asymmetric Synthesis, Wiley-VCH, 2005.
連結:
-
[7] B. List, Chem. Rev. 2007, 107, 5413-5415.
連結:
-
[8] P. I. Dalko, L. Moisan, Angew. Chem. Int. Ed. 2004, 43, 5138-5175.
連結:
-
[10] D. Enders, C. Grondal, M. R. Huttl, Angew. Chem. Int. Ed. 2007, 46, 1570-1581.
連結:
-
[11] P. I. Dalko, L. Moisan, Angew. Chem. Int. Ed. 2001, 40, 3726-3748.
連結:
-
[14] F. G. Fischer, A. Marschall, Berichte der deutschen chemischen Gesellschaft (A and B Series) 1931, 64, 2825-2827.
連結:
-
[15] H.-U. Blaser, B. Pugin, F. Spindler, J. Mol. Catal. A: Chem. 2005, 231, 1-20.
連結:
-
[17] M. Breuer, K. Ditrich, T. Habicher, B. Hauer, M. Kesseler, R. Sturmer, T. Zelinski, Angew. Chem. Int. Ed. 2004, 43, 788-824.
連結:
-
[18] H. Tye, P. J. Comina, J. Chem. Soc., Perkin Trans. 1 2001, 1729-1747.
連結:
-
[19] H. J. Federsel, Nat Rev Drug Discov 2005, 4, 685-697.
連結:
-
[20] D. W. MacMillan, Nature 2008, 455, 304-308.
連結:
-
[23] Y. Hayashi, T. Sumiya, J. Takahashi, H. Gotoh, T. Urushima, M. Shoji, Angew. Chem. Int. Ed. 2006, 45, 958-961.
連結:
-
[25] U. Kazmaier, Angew. Chem. Int. Ed. 2005, 44, 2186-2188.
連結:
-
[26] A. Berkessel, B. Koch, J. Lex, Adv. Synth. Catal. 2004, 346, 1141-1146.
連結:
-
[27] A. B. Northrup, I. K. Mangion, F. Hettche, D. W. MacMillan, Angew. Chem. Int. Ed. 2004, 43, 2152-2154.
連結:
-
[29] Z. Tang, Z. H. Yang, X. H. Chen, L. F. Cun, A. Q. Mi, Y. Z. Jiang, L. Z. Gong, Journal of the American Chemical Society 2005, 127, 9285-9289.
連結:
-
[31] Z. Tang, F. Jiang, L. T. Yu, X. Cui, L. Z. Gong, A. Q. Mi, Y. Z. Jiang, Y. D. Wu, Journal of the American Chemical Society 2003, 125, 5262-5263.
連結:
-
[33] S. Hanessian, V. Pham, Org. Lett. 2000, 2, 2975-2978.
連結:
-
[34] J. M. Betancort, C. F. Barbas, Org. Lett. 2001, 3, 3737-3740.
連結:
-
[37] S. P. Mathew, H. Iwamura, D. G. Blackmond, Angew. Chem. Int. Ed. 2004, 43, 3317-3321.
連結:
-
[41] B. List, C. Castello, Synlett 2001, 2001, 1687-1689.
連結:
-
[44] M. Movassaghi, E. N. Jacobsen, Science 2002, 298, 1904-1905.
連結:
-
[47] U. Eder, G. Sauer, R. Wiechert, Angew. Chem. Int. Ed. 1971, 10, 496-497.
連結:
-
[52] H. E. Zimmerman, M. D. Traxler, J. Am. Chem. Soc. 1957, 79, 1920-1923.
連結:
-
[56] A. H. Henseler, C. Ayats, M. A. Pericas, Adv. Synth. Catal. 2014, 356, 1795-1802.
連結:
-
[57] C. Kouklovsky, Y. Langlois, in Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd, 2001.
連結:
-
[61] F. Peng, Z. Shao, J. Mol. Catal. A: Chem. 2008, 285, 1-13.
連結:
-
[63] S. Luo, H. Xu, J. Li, L. Zhang, J. P. Cheng, Journal of the American Chemical Society 2007, 129, 3074-3075.
連結:
-
[64] S. Luo, H. Xu, L. Zhang, J. Li, J. P. Cheng, Organic Letters 2008, 10, 653-656.
連結:
-
[66] S. Hu, L. Zhang, J. Li, S. Luo, J.-P. Cheng, Eur. J. Org. Chem. 2011, 2011, 3347-3352.
連結:
-
[70] B. L. Zheng, Q. Z. Liu, C. S. Guo, X. L. Wang, L. He, Org Biomol Chem 2007, 5, 2913-2915.
連結:
-
[71] S. Luo, H. Xu, J. Li, L. Zhang, J. P. Cheng, J. Am. Chem. Soc. 2007, 129, 3074-3075.
連結:
-
[72] S. S. Ramasastry, K. Albertshofer, N. Utsumi, F. Tanaka, C. F. Barbas, 3rd, Angew. Chem. Int. Ed. 2007, 46, 5572-5575.
連結:
-
[73] S. S. Ramasastry, H. Zhang, F. Tanaka, C. F. Barbas, 3rd, Journal of the American Chemical Society 2007, 129, 288-289.
連結:
-
[75] S. Luo, H. Xu, J. Li, L. Zhang, J. P. Cheng, J Am Chem Soc 2007, 129, 3074-3075.
連結:
-
[76] P. Judeinstein, C. Sanchez, J. Mater. Chem. 1996, 6, 511-525.
連結:
-
[79] F. Hoffmann, M. Cornelius, J. Morell, M. Froba, Angew. Chem. Int. Ed. 2006, 45, 3216-3251.
連結:
-
[82] J. Y. Ying, C. P. Mehnert, M. S. Wong, Angew. Chem. Int. Ed. 1999, 38, 56-77.
連結:
-
[83] A. Corma, Chem. Rev. 1997, 97, 2373-2420.
連結:
-
[86] J. Jarupatrakorn, T. D. Tilley, J. Am. Chem. Soc. 2002, 124, 8380-8388.
連結:
-
[87] J. J. E. Moreau, M. Wong Chi Man, Coord. Chem. Rev. 1998, 178–180, Part 2, 1073-1084.
連結:
-
[91] X. Elias, R. Pleixats, M. W. C. Man, J. J. E. Moreau, Adv. Synth. Catal. 2006, 348, 751-762.
連結:
-
[95] R. J. P. Corriu, A. Mehdi, C. Reye, J. Mater. Chem. 2005, 15, 4285.
連結:
-
[96] D. Jiang, Q. Yang, H. Wang, G. Zhu, J. Yang, C. Li, J. Catal. 2006, 239, 65-73.
連結:
-
[97] C. Li, H. Zhang, D. Jiang, Q. Yang, Chem. Commun. 2007, 547-558.
連結:
-
[98] A. Molnar, B. Rac, Curr. Org. Chem. 2006, 10, 1697-1726.
連結:
-
[99] K. K. Sharma, T. Asefa, Angew. Chem. Int. Ed. 2007, 46, 2879-2882.
連結:
-
[105] R. Abu-Reziq, D. Avnir, J. Blum, Angew. Chem. Int. Ed. 2002, 41, 4132-4134.
連結:
-
[110] F. Calderon, R. Fernandez, F. Sanchez, A. Fernandez-Mayoralas, Adv. Synth. Catal. 2005, 347, 1395-1403.
連結:
-
[112] M. Gruttadauria, F. Giacalone, R. Noto, Chem. Soc. Rev. 2008, 37, 1666-1688.
連結:
-
[114] M. Benaglia, M. Cinquini, F. Cozzi, A. Puglisi, G. Celentano, Adv. Synth. Catal. 2002, 344, 533-542.
連結:
-
[117] J. Gao, J. Liu, D. Jiang, B. Xiao, Q. Yang, J. Mol. Catal. A: Chem. 2009, 313, 79-87.
連結:
-
[118] Y.-B. Zhao, L.-W. Zhang, L.-Y. Wu, X. Zhong, R. Li, J.-T. Ma, Tetrahedron: Asymmetry 2008, 19, 1352-1355.
連結:
-
[122] M. Kaik, J. Gawroński, Tetrahedron: Asymmetry 2003, 14, 1559-1563.
連結:
-
[123] R. Pedrosa, J. M. Andres, R. Manzano, D. Roman, S. Tellez, Organic & Biomolecular Chemistry 2011, 9, 935-940.
連結:
-
[126] N. Mase, N. Noshiro, A. Mokuya, K. Takabe, Adv. Synth. Catal. 2009, 351, 2791-2796.
連結:
-
[128] T. Kanemitsu, A. Umehara, M. Miyazaki, K. Nagata, T. Itoh, Eur. J. Org. Chem. 2011, 2011, 993-997.
連結:
-
[130] J. C. Latham, D. A. Markov, H. S. S?rensen, D. J. Bornhop, Angew. Chem. Int. Ed. 2006, 45, 955-958.
連結:
-
[131] A. J. Pearson, S. Panda, Org. Lett. 2011, 13, 5548-5551.
連結:
-
[132] J. Xu, X. Fu, C. Wu, X. Hu, Tetrahedron: Asymmetry 2011, 22, 840-850.
連結:
-
[134] M. Angeloni, O. Piermatti, F. Pizzo, L. Vaccaro, Eur. J. Org. Chem. 2014, 2014, 1716-1726.
連結:
-
[137] P. Muller, Pure Appl. Chem. 1994, 66.
連結:
-
[139] L. P. Hammett, J. Am. Chem. Soc. 1937, 59, 96-103.
連結:
-
References
-
[4] IUPAC, Compendium of Chemical Terminology 1997, 2nd ed.
-
[9] M. J. Gaunt, C. C. C. Johansson, A. McNally, N. T. Vo, Drug Discovery Today 2007, 12, 8-27.
-
[12] J. v. Liebig, Annalen der Chemie und Pharmacie 1860, 113, 246-267.
-
[13] W. Langenbeck, Angew. Chem. 1928, 41, 740-745.
-
[16] B. Schafer, H. Bernard, G. Bulow, U. E. Lange, H. Mack, T. Pfeiffer, W. Seitz, T. Zierke, Synthesis 2004, 2004, 2367-2375.
-
[21] S. Armando Cordova, Sweden; Jonas Hafren, Stockholm, Sweden.
-
[22] B. List, R. A. Lerner, C. F. Barbas, J. Am. Chem. Soc. 2000, 122, 2395-2396.
-
[24] G. Zhong, J. Fan, C. F. Barbas, Tetrahedron Lett. 2004, 45, 5681-5684.
-
[28] P. Krattiger, R. Kovasy, J. D. Revell, S. Ivan, H. Wennemers, Organic Letters 2005, 7, 1101-1103.
-
[30] E. Reyes, A. Cordova, Tetrahedron Lett. 2005, 46, 6605-6609.
-
[32] K. A. Ahrendt, C. J. Borths, D. W. C. MacMillan, J. Am. Chem. Soc. 2000, 122, 4243-4244.
-
[35] N. Mase, R. Thayumanavan, F. Tanaka, C. F. Barbas, 3rd, Organic Letters 2004, 6, 2527-2530.
-
[36] D. B. Ramachary, C. F. Barbas, 3rd, Organic Letters 2005, 7, 1577-1580.
-
[38] Y. Hayashi, J. Yamaguchi, K. Hibino, T. Sumiya, T. Urushima, M. Shoji, D. Hashizume, H. Koshino, Adv. Synth. Catal. 2004, 346, 1435-1439.
-
[39] N. S. Chowdari, J. T. Suri, C. F. Barbas, 3rd, Organic Letters 2004, 6, 2507-2510.
-
[40] Y. Hayashi, T. Urushima, M. Shoji, T. Uchimaru, I. Shiina, Adv. Synth. Catal. 2005, 347, 1595-1604.
-
[42] A. Cordova, W. Zou, I. Ibrahem, E. Reyes, M. Engqvist, W. W. Liao, Chem. Commun. 2005, 3586-3588.
-
[43] I. Ibrahem, W. Zou, M. Engqvist, Y. Xu, A. Cordova, Chemistry 2005, 11, 7024-7029.
-
[45] B. List, Tetrahedron 2002, 58, 5573-5590.
-
[46] J. Seayad, B. List, Organic & Biomolecular Chemistry 2005, 3, 719-724.
-
[48] Z. G. Hajos, D. R. Parrish, The Journal of Organic Chemistry 1974, 39, 1615-1621.
-
[49] N. Y. Yoichi M. A. Yamada, Hiroaki Sasai, and Masakatsu Shibasaki, Angew. Chem. Int. Ed. 1997, 36, 1871-1873.
-
[50] Y. M. A. Yamada, M. Shibasaki, Tetrahedron Lett. 1998, 39, 5561-5564.
-
[51] N. Yoshikawa, Y. M. A. Yamada, J. Das, H. Sasai, M. Shibasaki, J. Am. Chem. Soc. 1999, 121, 4168-4178.
-
[53] H. Sunden, I. Ibrahem, A. Cordova, Tetrahedron Lett. 2006, 47, 99-103.
-
[54] G. L. Zhao, Y. Xu, H. Sunden, L. Eriksson, M. Sayah, A. Cordova, Chemical Communications 2007, 734-735.
-
[55] S. Mitsumori, H. Zhang, P. Ha-Yeon Cheong, K. N. Houk, F. Tanaka, C. F. Barbas, J. Am. Chem. Soc. 2006, 128, 1040-1041.
-
[58] B. M. Trost, R. Radinov, E. M. Grenzer, J. Am. Chem. Soc. 1997, 119, 7879-7880.
-
[59] B. M. Trost, M. R. Machacek, A. Aponick, Acc. Chem. Res. 2006, 39, 747-760.
-
[60] P. Zhou, S. Luo, J. P. Cheng, Org Biomol Chem 2011, 9, 1784-1790.
-
[62] L. W. Xu, J. Luo, Y. Lu, Chemical Communications 2009, 1807-1821.
-
[65] S. Luo, Y. Qiao, L. Zhang, J. Li, X. Li, J.-P. Cheng, The Journal of Organic Chemistry 2009, 74, 9521-9523.
-
[67] F.-Z. Peng, Z.-H. Shao, X.-W. Pu, H.-B. Zhang, Adv. Synth. Catal. 2008, 350, 2199-2204.
-
[68] L. Li, L.-W. Xu, Y.-D. Ju, G.-Q. Lai, Synth. Commun. 2009, 39, 764-774.
-
[69] Y. Liu, J. Wang, Q. Sun, R. Li, Tetrahedron Lett. 2011, 52, 3584-3587.
-
[74] X. Ma, C.-S. Da, L. Yi, Y.-N. Jia, Q.-P. Guo, L.-P. Che, F.-C. Wu, J.-R. Wang, W.-P. Li, Tetrahedron: Asymmetry 2009, 20, 1419-1424.
-
[77] J. S. Beck, J. C. Vartuli, W. J. Roth, M. E. Leonowicz, C. T. Kresge, K. D. Schmitt, C. T. W. Chu, D. H. Olson, E. W. Sheppard, S. B. McCullen, J. B. Higgins, J. L. Schlenker, J. Am. Chem. Soc. 1992, 114, 10834-10843.
-
[78] C. T. Kresge, M. E. Leonowicz, W. J. Roth, J. C. Vartuli, J. S. Beck, Nature 1992, 359, 710-712.
-
[80] Q. Huo, D. I. Margolese, U. Ciesla, P. Feng, T. E. Gier, P. Sieger, R. Leon, P. M. Petroff, F. Schuth, G. D. Stucky, Nature 1994, 368, 317-321.
-
[81] Q. Huo, D. I. Margolese, U. Ciesla, D. G. Demuth, P. Feng, T. E. Gier, P. Sieger, A. Firouzi, B. F. Chmelka, Chem. Mater. 1994, 6, 1176-1191.
-
[84] H. H. P. Yiu, P. A. Wright, N. P. Botting, Microporous Mesoporous Mater. 2001, 44-45, 763-768.
-
[85] D. Zhao, J. Feng, Q. Huo, N. Melosh, G. H. Fredrickson, B. F. Chmelka, G. D. Stucky, Science 1998, 279, 548-552.
-
[88] A. Adima, J. J. E. Moreau, M. W. C. Man, Chirality 2000, 12, 411-420.
-
[89] C. Bied, D. Gauthier, J. J. E. Moreau, M. W. Chi Man, J. Sol-Gel Sci. Technol. 2001, 20, 313-320.
-
[90] J. J. E. Moreau, L. Vellutini, M. W. Chi Man, C. Bied, J.-L. Bantignies, P. Dieudonne, J.-L. Sauvajol, J. Am. Chem. Soc. 2001, 123, 7957-7958.
-
[92] B. J. Melde, B. T. Holland, C. F. Blanford, A. Stein, Chem. Mater. 1999, 11, 3302-3308.
-
[93] T. Asefa, M. J. MacLachlan, N. Coombs, G. A. Ozin, Nature 1999, 402, 867-871.
-
[94] A. Stein, B. J. Melde, R. C. Schroden, Adv. Mater. 2000, 12, 1403-1419.
-
[100] K. K. Sharma, A. Anan, R. P. Buckley, W. Ouellette, T. Asefa, J. Am. Chem. Soc. 2008, 130, 218-228.
-
[101] P. Yu, J. He, C. Guo, Chem. Commun. 2008, 2355-2357.
-
[102] D. Pini, A. Mandoli, S. Orlandi, P. Salvadori, Tetrahedron: Asymmetry 1999, 10, 3883-3886.
-
[103] K. Yu, Z. Gu, R. Ji, L.-L. Lou, S. Liu, Tetrahedron 2009, 65, 305-311.
-
[104] J. Yan, L. Wang, Chirality 2009, 21, 413-420.
-
[106] J. M. Notestein, A. Katz, Chemistry 2006, 12, 3954-3965.
-
[107] A. Zamboulis, N. J. Rahier, M. Gehringer, X. Cattoen, G. Niel, C. Bied, J. J. E. Moreau, M. W. C. Man, Tetrahedron: Asymmetry 2009, 20, 2880-2885.
-
[108] E. L. Margelefsky, R. K. Zeidan, V. Dufaud, M. E. Davis, J. Am. Chem. Soc. 2007, 129, 13691-13697.
-
[109] E. L. Margelefsky, A. Bendjeriou, R. K. Zeidan, V. Dufaud, M. E. Davis, J. Am. Chem. Soc. 2008, 130, 13442-13449.
-
[111] E. G. Doyaguez, F. Calderon, F. Sanchez, A. Fernandez-Mayoralas, The Journal of Organic Chemistry 2007, 72, 9353-9356.
-
[113] D. Dhar, I. Beadham, S. Chandrasekaran, Journal of Chemical Sciences 2003, 115, 365-372.
-
[115] D. Font, C. Jimeno, M. A. Pericas, Org. Lett. 2006, 8, 4653-4655.
-
[116] E. Adi Prasetyanto, S. C. Lee, S. M. Jeong, S. E. Park, Chem. Commun. 2008, 1995-1997.
-
[119] P. Li, L. Wang, Y. Zhang, G. Wang, Tetrahedron 2008, 64, 7633-7638.
-
[120] C. Yeh., National Taiwan Univeristy 2013.
-
[121] S. Luo, X. Zheng, J.-P. Cheng, Chem. Commun. 2008, 5719-5721.
-
[124] Z. Jiang, H. Yang, X. Han, J. Luo, M. W. Wong, Y. Lu, Organic & Biomolecular Chemistry 2010, 8, 1368-1377.
-
[125] H.-H. Li, Y.-H. He, Z. Guan, Catal. Commun. 2011, 12, 580-582.
-
[127] N. Mase, Y. Nakai, N. Ohara, H. Yoda, K. Takabe, F. Tanaka, C. F. Barbas, J. Am. Chem. Soc. 2006, 128, 734-735.
-
[129] Y. Akira, N. Yoshinari, A. Kenichi, W. Manabu, K. Hiromi, Y. Hisashi, Bull. Chem. Soc. Jpn. 2001, 74, 1477-1484.
-
[133] T. Miura, H. Kasuga, K. Imai, M. Ina, N. Tada, N. Imai, A. Itoh, Organic & Biomolecular Chemistry 2012, 10, 2209-2213.
-
[135] C. Yeh, Y. R. Sun, S. J. Huang, Y. M. Tsai, S. Cheng, Chem. Commun. 2015, 51, 17116-17119.
-
[136] Y.-R. Luo, in Comprehensive Handbook of Chemical Bond Energies, CRC Press, 2007, pp. 455-480.
-
[138] F. R. Jensen, C. H. Bushweller, B. H. Beck, J. Am. Chem. Soc. 1969, 91, 344-351.
-
[140] K. Kandel, S. M. Althaus, C. Peeraphatdit, T. Kobayashi, B. G. Trewyn, M. Pruski, I. I. Slowing, J. Catal. 2012, 291, 63-68.
|