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包春燕*, 贾慧娟, 刘涛, 汪奕, 彭伟, 朱麟勇. 双分子层膜人工离子通道的合成[J]. 化学进展, 2012, 24(07): 1337-1345.
Bao Chunyan, Jia Huijuan, Liu Tao, Wang Yi, Peng Wei, Zhu Linyong. Synthesis of Artificial Ion Channels in Bilayer Membrane[J]. Progress in Chemistry, 2012, 24(07): 1337-1345.
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[1] Eisenberg B. Acc. Chem. Res., 1998, 31(3): 117-123[2] 张宗明(Zhang Z M), 裘法祖(Qiu F Z). 世界华人消化杂志(World Chinese Journal of Digestology), 2005, 13(5): 585-587[3] Chorbachi R, Graham J M, Ford J, Raine C H. Int. J. Pediatr. Otorhinolaryngol, 2002, 66(3): 213-221[4] Swift P A, MacGregor G A. Am. J. Pharmacogenomics, 2004, 4(3): 161-168[5] Tabushi I, Kuroda Y, Yokota K. Tetrahedron Letters, 1982, 23(44): 4601-4604[6] Fernandez-Lopez S, Kim H S, Choi E C, Delgado M, Granja J R, Khasanov A, Kraehenbuehl K, Long G, Weinberger D A, Wilcoxen K M, Ghadiri M R. Nature, 2001, 412(6845): 452-455[7] Cornell B A, Braach-Maksvytis V L B, King L G, Osman P D J, Raguse B, Wieczorek L, Pace R J. Nature, 1997, 387(6633): 580-583[8] Das G, Talukdar P, Matile S. Science, 2002, 298(5598): 1600-1602[9] Boudreault P L, Arseneault M, Otis F, Voyer N. Chem. Commun., 2008, 2118-2120[10] Leevy W M, Donato G M, Ferdani R, Goldman W E, Schlesinger P H, Gokel G W. J. Am. Chem. Soc., 2002, 124(31): 9022-9023[11] Leevy W M, Gammon S T, Levchenko T, Daranciang D D, Murillo O, Torchilin V, Piwnica-Worms D, Huettner J E, Gokel G W. Org. Biomol. Chem., 2005, 3(19): 3544-3550[12] Smith B A, Daschbach M M, Gammon S T, Xiao S Z, Chapman S E, Hudson C, Suckow M, Piwnica-Worms D, Gokel G W, Leevy W M. Chem. Commun., 2011, 7977-7979[13] Sisson A L, Shah M R, Bhosalea S, Matile S. Chem. Soc. Rev., 2006, 35(12): 1269-1286[14] Chui J K W, Fyles T M. Chem. Soc. Rev., 2011, 46(23), 4169-4171[15] Andrea H D, Andrea K, Koert U. ChemBioChem, 2001, 2(3): 221-223[16] Arndt H D, Vescovi A, Schrey A, Pfeifer J R, Koert U. Tetrahedron, 2002, 58(14): 2789-2801[17] Koert U, Rei P. Journal of Supramolecular Chemistry, 2002, 2(1/3): 29-37[18] Koert U. Physical Chemistry Chemical Physics, 2005, 7(7): 1501-1506[19] Essen L O, Koert U. Annu. Rep. Prog. Chem., Sect. C: Phys. Chem., 2008, 104: 165-188[20] Borisenko V, Burns D C, Zhang Z H, Woolley G A. J. Am. Chem. Soc., 2000, 122(27): 6364-6370[21] Lougheed T, Borisenko V, Hennig T, Rück-Braunb K, Woolley G A. Org. Biomol. Chem., 2004, 2(19): 2798-2801[22] Koer A, Walko M, Merjbeg W, Feringa B L. Science, 2005, 309(5735): 755-758[23] Madhavant N, Robert E C, Gin M S. Angew. Chem. Int. Ed., 2005, 44(46): 7584-7587[24] Jog P V, Gin M S. Org. Lett., 2008, 10(17): 693-3696[25] Nakano A, Xie Q, Mallen J V, Echegoyen L, Gokel G W. J. Am. Chem. Soc., 1990, 112(3): 1287-1289[26] Gokel G W, Schlesinger P H, Djedovic N K, Ferdani R, Harder E C, Hu J, Leevy W M, Pajewska J, Pajewski R, Weber M E. Bioorg. Med. Chem., 2004, 12(6): 1291-1304[27] Weber M E, Schlesinger P H, Gokel G W. J. Am. Chem. Soc., 2005, 127(2): 636-642[28] Leevy W M, Weber M E, Schlesinger P H, Gokel G W. Chem. Commun., 2005, 89-91[29] Wang W, Li R, Gokel G W. Chem. Eur. J., 2009, 15(40): 10543-10553[30] Atkins J L, Patel M B, Cusumano Z, Gokel G W. Chem. Commun., 2010, 8166-8167[31] Sakai N, Gerard D, Matile S. J. Am. Chem. Soc., 2001, 123(11): 2517-2524[32] Sakai N, Matile S. J. Am. Chem. Soc., 2002, 124(7): 1184-1185[33] Hall A C, Suarez C, Hom-Choudhury A, Manu A N A, Hall C D, Kirkovits G J, Ghiriviga I. Org. Biomol. Chem., 2003, 1(16): 2973-2982[34] Jeon Y J, Ki H, Jon S, Selvapalam N, Oh D Y, Seo I, Park C S, Jung S R, Koh D S, Kim K. J. Am. Chem. Soc., 2004, 126(49): 15944-15945[35] Maulucci N, Riccardis F D, Botta C B, Casapullo A, Cressina E, Fregonese M, Tecilla P, Izzo I. Chem. Commun., 2005, 1354-1356[36] Yano M, Tong C C, Light M E, Schmidtchen F P, Gale P A. Org. Biomol. Chem., 2010, 8(19): 4356-4363[37] Gale P A. Accounts of Chemical Research, 2011, 44(3): 216-226[38] Fyles T M, Loock D, Zhou X. J. Am. Chem. Soc., 1998, 120(13): 997-3003[39] Goto C, Yamamura M, Satake A, Kobuke Y. J. Am. Chem. Soc., 2001, 123(11): 2517-2524[40] 金培元(Jin P Y), 巨勇(Ju Y). 化学进展(Progress in Chemistry), 2007, 19: 1883-1895[41] Sakai N, Houdebert D, Matile S. Chem. Eur. J., 2003, 9(1): 223-232[42] Matile S, Jentzsch A V, Montenegr J, Fin A. Chem. Soc. Rev., 2011, 40(5): 2453-2474[43] Henning A, Ficher L, Guichard G, Matile S. J. Am. Chem. Soc., 2009, 131(46): 16889-16895[44] Ghadiri M R, Grarji J R, Buehler L K. Nature, 1994, 369: 301-304[45] Fernandez-Lopez S, Kim H S, Choi E C, Delgado M, Granja J R, Khasanov A, Kraehenbuehl K, Long G, Weinberger D A, Wilcoxen K M, Ghadiri M R. Nature, 2001, 412: 452-455[46] 唐敏(Tang M), 樊建芬(Fan J F), 刘健(Liu J), 何梁君(He L J), 何珂(He K). 化学进展(Progress in Chemistry), 2010, 22: 648-653[47] Cazacu A, Tong C, Lee A V D, Fyles T M, Barboiu M. J. Am. Chem. Soc., 2006, 128(29): 9541-9548[48] Helsel A J, Brown A L, Yamato K, Feng W, Yuan L H, Clements A J, Harding S V, Szabo G, Shao Z F, Gong B. J. Am. Chem. Soc., 2008, 130(47): 15784-15785[49] Haynes C J E, Gale P A. Chem. Commun., 2011, 8203-8209[50] Davis J T, Okunola O, Quesada R. Chem. Soc. Rev., 2010, 39(10): 3843-3862[51] Hou X, Guo W, Jiang L. Chem. Soc. Rev., 2011, 40: 2385-2401[52] Hou X, Jiang L. ACS Nano, 2009, 3 (11): 3339-3342[53] Xia F, Guo W, Mao Y D, Hou X, Xue J M, Xia H W, Wang L, Song Y L, Ji H, Qi O Y, Wang Y G, Jiang L. J. Am. Chem. Soc., 2008, 130(26): 8345-8350[54] Hou X, Guo W, Xia F, Nie F Q, Dong H, Tian Y, Wen L, Wang L, Cao L, Yang Y, Xue J, Song Y, Wang Y, Liu D, Jiang L. J. Am. Chem. Soc., 2009, 131(22): 7800-7805[55] Hou X, Yang F, Li L, Song Y L, Jiang L, Zhu D B. J. Am. Chem. Soc., 2010, 132: 11736-11742[56] Hou X, Liu Y J, Dong H, Yang F, Li L, Jiang L. Adv. Mater., 2010, 22: 2440-2243 |
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