• 超分子化学专辑 •
邹怀波, 汪华华, 梅光泉, 刘海洋, 张启光. 铁咔咯配合物在有机合成中的催化应用[J]. 化学进展, 2015, 27(6): 666-674.
Zou Huaibo, Wang Huahua, Mei Guangquan, Liu Haiyang, Chang Chi-Kwong. Catalytic Application of Iron Corrole Complexes in Organic Synthesis[J]. Progress in Chemistry, 2015, 27(6): 666-674.
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[1] Cuesta L, Sessler J L. Chem. Soc. Rev., 2009, 38: 2716. [2] (a) Nakamura Y, Aratani N, Osuka A. Chem. Soc. Rev., 2007, 36: 831; (b) Pareek Y, Ravikanth M, Chandrashekar T K. Acc. Chem. Res., 2012, 45: 1801; (c) Zha Q Z, Ding C X, Rui X, Xie Y S. Cryst. Growth Des., 2013, 13: 4583; (d) Wei P C, Zhang K, Li X, Meng D Y, Ögren H, Ou Z P, Ng S, Furuta H, Xie Y S. Angew. Chem. Int. Ed., 2014, 53: 14069; (e) Zha Q Z, Rui X, Wei T T, Xie Y S. Cryst. Eng. Comm., 2014, 16: 7371. [3] Ethirajan M, Chen Y H, Joshi P, Pandey R K. Chem. Soc. Rev., 2011, 40: 340. [4] (a) Li L L, Diau E W G. Chem. Soc. Rev., 2013, 42: 291; (b) Wang Y Q, Chen B, Wu W J, Li X, Zhu W H, Tian H, Xie Y S. Angew. Chem. Int. Ed., 2014, 53: 10779; (c) Sun X, Wang Y Q, Li X, Ögren H, Zhu W H, Tian H, Xie Y S. Chem. Commun., 2014, 50: 15609. [5] (a) Shin J Y, Kim K S, Yoon M C, Lim J M, Yoon Z S, Osuka A, Kim D. Chem. Soc. Rev., 2010, 39: 2751; (b) De la Torre G, Bottari G, Sekita M, Hausmann A, Guldi D M, Torres T. Chem. Soc. Rev., 2013, 42: 8049. [6] (a) Lu H J, Zhang X P. Chem. Soc. Rev., 2011, 40: 1899; (b) Chan K H, Guan X G, Lo V K Y, Che C M. Angew. Chem. Int. Ed., 2014, 53: 2982; (c) Fackler P, Huber S M, Bach T. J. Am. Chem. Soc., 2012, 134: 12869. [7] Tanaka T, Osuka A. Chem. Soc. Rev., 2015, 44: 943. [8] Johnson A W, Kay I T. J. Chem. Soc., 1965, 1620. [9] (a) Gross Z, Galili N, Saltsman I. Angew. Chem. Int. Ed., 1999, 38: 1427; (b) Gryko D T, Koszarna B. Org. Biomol. Chem., 2003, 1: 350. [10] (a) Gross Z, Gray H B. Adv. Synth. Catal., 2004, 346: 165; (b) Zdilla M J, Abu-Omar M M. J. Am. Chem. Soc., 2006, 128: 16971; (c) Mahammed A, Gross Z. Angew. Chem. Int. Ed., 2006, 45: 6544; (d) He C L, Ren F L, Zhang X B, Han Z X. Talanta, 2006, 70: 364; (e) Zhang X B, Han Z X, Fang Z H, Shen G L, Yu R Q. Anal. Chim. Acta, 2006, 562: 210; (f) Li C Y, Zhang X B, Han Z X, Ökermark B, Sun L C, Shen G L, Yu R Q. Analyst, 2006, 131: 388; (g) Aviv I, Gross Z. Chem. Commun., 2007, 1987; (h) Paolesse R. Synlett, 2008, 15: 2215; (i) Flamigni L, Gryko D T. Chem. Soc. Rev., 2009, 38: 1635; (j) Aviv-Harel I, Gross Z. Chem. Eur. J., 2009, 15: 8382; (k) Abu-Omar M M. Dalton Trans., 2011, 40: 3435; (l) Liu H Y, Mahmood M H, Qiu S X (Samuel), Chang C K. Coordin. Chem. Rev., 2013, 257: 1306. [11] (a) Gross Z, Gray H B. Comment. Inorg. Chem., 2006, 27: 61; (b) Rabinovich E, Goldberg I, Gross Z. Chem. Eur. J., 2011, 17: 12294; (c) Nigel-Etinger I, Goldberg I, Gross Z. Inorg. Chem., 2012, 51: 1983. [12] Palmer J H, Brock-Nannestad T, Mahammed A, Durrell A C, VanderVelde D, Virgil S, Gross Z, Gray H B. Angew. Chem. Int. Ed., 2011, 50: 9433. [13] Agadjanian H, Ma J, Rentsendorj A, Valluripalli V, Hwang J Y, Mahammed A, Farkas D L, Gray H B, Gross Z, Medina-Kauwe L K. Proc. Natl. Acad. Sci. USA, 2009, 106: 6105. [14] (a) Fu B Q, Huang J, Ren L G, Weng X C, Zhou Y Y, Du Y H, Wu X J, Zhou X, Yang G F. Chem. Commun., 2007, 3264; (b) Fu B Q, Zhang D, Weng X C, Zhang M, Ma H, Ma Y Z, Zhou X. Chem. Eur. J., 2008, 14: 9431; (c) Ma H, Zhang M, Zhang D, Huang R, Zhao Y, Yang H, Liu Y J, Weng X C, Zhou Y Y, Deng M G, Zhou X. Chem. Asian J., 2010, 5: 114. [15] (a) Zhang Y, Wang Q, Wen J Y, Wang X L, Mahmood M H R, Ji L N, Liu H Y. Chin. J. Chem., 2013, 31: 1321; (b) Zhang Y, Chen H, Wen J Y, Wang X L, Wang H, Ji L N, Liu H Y. Chem. J. Chin. Univ., 2013, 34: 2462; (c) Zhang Y, Wen J Y, Wang X L, Mahmood M H R, Liu Z Y, Wang H, Ji L N, Liu H Y. Appl. Organometal. Chem., 2014, 28: 559. [16] Basumatary B, Kaloo M A, Singh V K, Mishra R, Murugavel M, Sankar J. RSC Adv., 2014, 4: 28417. [17] Chen G Q, Xu Z J, Zhou C Y, Che C M. Chem. Commun., 2011, 47: 10963. [18] Liu H Y, Lai T S, Yeung L L, Chang C K. Org. Lett., 2003, 5: 617. [19] Zhan H Y, Liu H Y, Chen H J, Jiang H F. Tetrahedron Lett., 2009, 50: 2196. [20] Lian P, Liu H Y, Liu L Y, Shi L, Jiang H F, Chang C K. Chin. Chem. Lett., 2009, 20: 21. [21] Shi L, Liu H Y, Shen H, Hu J, Zhang G L, Wang H, Ji L N, Chang C K, Jiang H F. J. Porph. Phthal., 2009, 13: 1221. [22] Zhan H Y, Liu H Y, Lu J, Wang A Z, You L L, Wang H, Ji L N, Jiang H F. J. Porph. Phthal., 2010, 14: 150. [23] Shi L, Liu H Y, Peng K M, Wang X L, You L L, Lu J, Zhang L, Wang H, Ji L N, Jiang H F. Tetrahedron Lett., 2010, 51: 3493. [24] Lu J, Liu H Y, Shi L, Wang X L, Ying X, Zhang L, Ji L N, Zang L Q, Chang C K. Chin. Chem. Lett., 2011, 22: 101. [25] Mahmood M H R, Liu Z Y, Liu H Y, Zou H B, Chang C K. Chin. Chem. Lett., 2014, 25: 1349. [26] Liu H Y, Chen L, Yam F, Zhan H Y, Ying X, Wang X L, Jiang H F, Chang C K. Chin. Chem. Lett., 2008, 19: 1000. [27] Liu H Y, Yam F, Xie Y T, Li X Y, Chang C K. J. Am. Chem. Soc., 2009, 131: 12890. [28] Liu H Y, Zhou H, Liu L Y, Ying X, Jiang H F, Chang C K. Chem. Lett., 2007, 36: 274. [29] Ng N C, Mahmood M H R, Liu H Y, Yam F, Yeung L L, Chang C K. Chin. Chem. Lett., 2014, 25: 571. [30] Yu L, Wang Q, Dai L, Li W Y, Chen R, Mahmood M H R, Liu H Y, Chang C K. Chin. Chem. Lett., 2013, 24: 447. [31] Wang Q, Zhang Y, Yu L, Yang H, Mahmood M H R, Liu H Y. J. Porph. Phthal., 2014, 18: 316. [32] Gross Z, Simkhovich L. Chem. Commun., 1999, 599. [33] Biswas A N, Das P, Agarwala A, Bandyopadhyay D, Bandyopadhyay P. J. Mol. Catal. A: Chem., 2010, 326: 94. [34] Biswas A N, Pariyar A, Bose S, Das P, Bandyopadhyay P. Catal. Commun., 2010, 11: 1008. [35] Pariyar A, Bose S, Biswas A N, Das P, Bandyopadhyay P. Catal. Commun., 2013, 32: 23. [36] Bose S, Pariyar A, Biswas A N, Bandyopadhyay P. J. Mol. Catal. A: Chem., 2013, 378: 179. [37] (a) Anding B J, Ellern A, Woo L K. Organometallics, 2012, 31: 3628; (b) Xu X, Lu H J, Ruppel J V, Cui X, de Mesa S L, Wojtas L, Zhang X P. J. Am. Chem. Soc., 2011, 133: 15292; (c) Ruppel J V, Gauthier T J, Snyder N L, Perman J A, Zhang X P. Org. Lett., 2009, 11: 2273; (d) Zhu S F, Ruppel J V, Lu H J, Wojtas L, Zhang X P. J. Am. Chem. Soc., 2008, 130: 5042; (e) Zhu S F, Perman J A, Zhang X P. Angew. Chem. Int. Ed., 2008, 47: 8460; (f) Chen Y, Zhang X P. J. Org. Chem., 2007, 72: 5931. [38] (a) Chen Y, Fields K B, Zhang X P. J. Am. Chem. Soc., 2004, 126: 14718; (b) Chen Y, Ruppel J V, Zhang X P. J. Am. Chem. Soc., 2007, 129: 12074; (c) Chattopadhyay P, Matsuo T, Tsuji T, Ohbayashi J, Hayashi T. Organometallics, 2011, 30: 1869. [39] (a) Morandi B, Carreira E M. Science, 2012, 335: 1471; (b) Morandi B, Carreira E M. Angew. Chem. Int. Ed., 2010, 49: 938; (c) Morandi B, Dolva A, Carreira E M. Org. Lett., 2012, 14: 2162; (d) Morandi B, Cheang J. Carreira E M. Org. Lett., 2011, 13: 3080. [40] Simkhovich L, Mahammed A, Goldberg I, Gross Z. Chem. Eur. J., 2001, 7: 1041. [41] (a) Vyas R, Gao G Y, Harden J D, Zhang X P. Org. Lett., 2004, 6: 1907; (b) Gao G Y, Jones J E, Vyas R, Harden J D, Zhang X P. J. Org. Chem., 2006, 71: 6655; (c) Ruppel J V, Jones J E, Huff C A, Kamble R M, Chen Y, Zhang X P. Org. Lett., 2008, 10: 1995; (d) Jones J E, Ruppel J V, Gao G Y, Moore T M, Zhang X P. J. Org. Chem., 2008, 73: 7260. [42] Liu P, Wong E L M, Yuen A W H, Che C M. Org. Lett., 2008, 10: 3275. [43] Simkhovich L, Gross Z. Tetrahedron Lett., 2001, 42: 8089. [44] Liang L, Lv H B, Yu Y, Wang P, Zhang J L. Dalton Trans., 2012, 41: 1457. [45] (a) Baumann L K, Mbuvi H M, Du G D, Woo L K. Organometallics, 2007, 26: 3995; (b) Lu H J, Jiang H L, Wojtas L, Zhang X P. Angew. Chem. Int. Ed., 2010, 49: 10192; (c) Lyaskovsky V, Suarez A I O, Lu H J, Jiang H L, Zhang X P, de Bruin B. J. Am. Chem. Soc., 2011, 133: 12264; (d) Lu H J, Jiang H L, Hu Y, Wojtas L, Zhang X P. Chem. Sci., 2011, 2: 2361; (e) Lu H J, Hu Y, Jiang H L, Wojtas L, Zhang X P. Org. Lett., 2012, 14: 5158. [46] Aviv I, Gross Z. Synlett., 2006, 6: 951. [47] Aviv I, Gross Z. Chem. Eur. J., 2008, 14: 3995. [48] Kuwano T, Kurahashi T, Matsubara S. Chem. Lett., 2013, 42: 1241. [49] Nakano K, Kobayahi T, Ohkawara T, Imoto H, Nozaki K. J. Am. Chem. Soc., 2013, 135: 8456. [50] (a) Mirafzal G A, Cheng G L, Woo L K. J. Am. Chem. Soc., 2002, 124: 176; (b) Cheng G L, Mirafzal G A, Woo L K. Organometallics, 2003, 22: 1468; (c) Chen Y, Huang L Y, Ranade M A, Zhang X P. J. Org. Chem., 2003, 68: 3714; (d) Chen Y, Huang L Y, Zhang X P. Org. Lett., 2003, 5: 2493. [51] Tachinami T, Nishimura T, Ushimaru R, Noyori R, Naka H. J. Am. Chem. Soc., 2013, 135: 50. [52] Wakabayashi R, Kurahashi T, Matsubara S. Org. Lett., 2012, 14: 4794. [53] Wang J W, Meng F H, Zhang L F. Organometallics, 2009, 28: 2334. [54] Venkatasubbaiah K, Zhu X J, Kays E, Hardcastle K I, Jones C W. ACS Catal., 2011,1: 489. |
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