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刘艳红, 周林成, 惠新平, 赵光辉, 李彦锋. 超顺磁性纳米催化剂在有机合成中的应用[J]. 化学进展.
Liu Yanhong, Zhou Lincheng, Hui Xinping, Zhao Guanghui, Li Yanfeng. Applications of Superparamagnetically Separable Nano-Catalysts in Organic Synthesis[J]. Progress in Chemistry.
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[1] Gladysz J A. Chem. Rev., 2002, 102 (10): 3215-3216[2] Schlögl R, Abd Hamid S B. Angew. Chem. Int. Ed., 2004, 43 (13): 1628-1637[3] Bell A T. Science, 2003, 299 (5613): 1688-1691[4] Cui X, Li J, Zhang Z P, Fu Y, Liu L, Guo Q X. J. Org. Chem., 2007, 72 (24): 9342-9345[5] Ye J, Chen W, Wang D. Dalton Trans., 2008, (30): 4015-4022[6] de Vries J G. Dalton Trans., 2006, (3): 421-429[7] Zhang Z J, Wang Z L, Chakoumakos B C, Yin J S. J. Am. Chem. Soc., 1998, 120 (8): 1800-1804[8] Cui Y J, Li Y F, Yang Y, Liu X, Lei L, Zhou L C, Pan F. J. Bioch., 2010, 150 (1): 171-174[9] Shi F, Tse M K, Pohl M M, Brückner A, Zhang S, Beller M. Angew. Chem. Int. Ed., 2007, 46 (46): 8866-8868[10] Reddy B V S, Krishna A S, Ganesh A V, Kumar G G K S N. Tetrahedron Lett., 2011, 52 (12): 1359-1362[11] Bedford R B, Betham M, Bruce D W, Davis S A, Frost R M, Hird M. Chem. Commun., 2006, (13): 1398-1400[12] Tong J H, Bo L L, Li Z, Lei Z Q, Xia C G. J. Mol. Catal. A Chem., 2009, 307 (1/2): 58-63[13] Liu J, Peng X, Sun W, Zhao Y, Xia C. Org. Lett., 2008, 10 (18): 3933-3936[14] 刘诗咏(Liu S Y), 吴家守(Wu J S), 蒋华江(Jiang H J), 金正能(Jin Z N), 姜玄珍(Jiang X Z). 有机化学(Chin. J. Org. Chem. ), 2009, 29 (10) : 1587-1592[15] Zhang J L, Wang Y, Ji H, Wei Y G, Wu N Z, Zuo B J, Wang Q L. J. Catal., 2005, 229 (1): 114-118[16] Zhang D H, Li G D, Li J X, Chen J S. Chem. Commun., 2008, (29): 3414-3416[17] Kotani M, Koike T, Yamaguchi K, Mizuno N. Green Chem., 2006, 8 (8): 735-741[18] Jun CH, Park Y J, Yeon YR, Choi JR, Lee WR, Ko SJ, Cheon J. Chem. Commun., 2006, (15): 1619-1621[19] Polshettiwar V, Baruwati B, Varma R S. Chem. Commun., 2009, (14): 1837-1839[20] Baruwati B, Guin D, Manorama S V. Org. Lett., 2007, 9 (26): 5377-5380[21] Polshettiwar V, Varma R S. Org. Biomol. Chem., 2009, 7 (1): 37-40[22] Guin D, Baruwati B, Manorama S V. Org. Lett., 2007, 9 (7): 1419-1421[23] Polshettiwar V, Baruwati B, Varma R S. Green Chem., 2009, 11 (1): 127-131[24] Baruwati B, Polshettiwar V, Varma R S. Tetrahedron Lett., 2009, 50 (11): 1215-1218[25] Polshettiwar V, Varma R S. Chem. Eur. J., 2009, 15 (7): 1582-1586[26] Gleeson O, Tekoriute R, Gun'ko Y K, Connon S J. Chem. Eur. J., 2009, 15 (23): 5669-5673[27] Stevens P D, Li G, Fan J, Yen M, Gao Y. Chem. Commun., 2005, (35): 4435-4437[28] Wang Z, Shen B, Aihua Z, He N. Chem. Eng. J., 2005, 113 (1): 27-34[29] Luo S Z, Zheng X X, Cheng J P. Chem. Commun., 2008, (44): 5719-5721[30] Ding S J, Xing Y C, Radosz M, Shen Y Q. Macromolecules, 2006, 39 (19): 6399-6405[31] Kassaee M Z, Masrouri H, Movahedi F. Appl. Catal. A-Gen., 2011, 395 (1/2): 28-33[32] Phan N T S, Gill C S, Nguyen J V, Zhang Z J, Jones C W. Angew. Chem., 2006, 118 (14): 2267-2270[33] Abu-Reziq R, Wang D, Post M, Alper H. Chem. Mater., 2008, 20 (7): 2544-2550[34] Abu-Reziq R, Wang D, Post M, Alper H. Adv. Synth. Catal., 2007, 349 (13): 2145-2150[35] Hu A G, Yee G T, Lin W B. J. Am. Chem. Soc., 2005, 127 (36): 12486-12487[36] Laska U, Frost C, Plucinski P, Price G. Catal. Lett., 2008, 122 (1): 68-75[37] Yoon T J, Lee W, Oh Y S, Lee J K. New J. Chem., 2003, 27 (2): 227-229[38] Chouhan G, Wang D S, Alper H. Chem. Commun., 2007, (45): 4809-4811[39] Zhu Y H, Peng S C, Emi A, Su Z S, Monalisa, Kemp R A. Adv. Synth. Catal., 2007, 349 (11/12): 1917-1922[40] Wang Y H, Lee J K. J. Mol. Catal. A Chem., 2007, 263 (1/2): 163-168[41] Yeo K M, Lee S I, Lee Y T, Chung Y K, Lee I S. Chem. Lett., 2008, 37 (1): 116-117[42] Arai T, Sato T, Kanoh H, Kaneko K, Oguma K, Yanagisawa A. Chem. Eur. J., 2008, 14 (3): 882-885[43] Kim J, Lee J E, Lee J, Jang Y, Kim S W, An K, Yu J H, Hyeon T. Angew. Chem., 2006, 118 (29): 4907-4911[44] Yi D K, Lee S S, Ying J Y. Chem. Mater., 2006, 18 (10): 2459-2461[45] Rossi L M, Silva F P, Vono L L R, Kiyohara P K, Duarte E L, Itri R, Landers R, Machado G. Green Chem., 2007, 9 (4): 379-385[46] Jacinto M J, Kiyohara P K, Masunaga S H, Jardim R F, Rossi L M. Appl. Catal. A-Gen., 2008, 338 (1/2): 52-57[47] Jacinto M J, Santos O, Jardim R F, Landers R, Rossi L M. Appl. Catal. A-Gen., 2009, 360 (2): 177-182[48] Tang H, Yu C H, Oduoro W, He H, Tsang S C. Langmuir, 2008, 24 (5): 1587-1590[49] Mori K, Sugihara K, Kondo Y, Takeuchi T, Morimoto S, Yamashita H. J. Phys. Chem. C, 2008, 112 (42): 16478- 16483[50] Jiang Y J, Gao Q M. J. Am. Chem. Soc., 2006, 128 (3): 716-717[51] Zhou L, Gao C, Xu W. Langmuir, 2010, 26 (13): 11217-11225[52] Shokouhimehr M, Piao Y, Kim J, Jang Y, Hyeon T. Angew. Chem., 2007, 119 (37): 7169-7173[53] Park J C, Lee H J, Jung H S, Kim M, Kim H J, Park K H, Song H. ChemCatChem, 2011, 3 (4): 755-760[54] Lv G, Mai W, Jin R, Gao L. Synlett, 2008, (9): 1418-1422[55] Schätz A, Hager M, Reiser O. Adv. Funct. Mater., 2009, 19 (13): 2109-2115[56] Abu-Reziq R, Alper H, Wang D S, Post M L. J. Am. Chem. Soc., 2006, 128 (15): 5279-5282[57] García-Garrido S E, Francos J, Cadierno V, Basset J M, Polshettiwar V. ChemSusChem, 2011, 4 (1): 104-111[58] Li J, Zhang Y M, Han D F, Gao Q, Li C. J. Mol. Catal. A Chem., 2009, 298 (1/2): 31-35[59] Shylesh S, Schweizer J, Demeshko S, Schünemann V, Ernst S, Thiel W R. Adv. Synth. Catal., 2009, 351 (11/12): 1789-1795[60] Kawamura M, Sato K. Chem. Commun., 2006, (45): 4718-4719[61] Izatt R M, Pawlak K, Bradshaw J S, Bruening R L. Chem. Rev., 1995, 95 (7): 2529-2586[62] Kawamura M, Sato K. Chem. Commun., 2007, (32): 3404-3405[63] Neatu F, Kraynov A, D'Souza L, Parvulescu V I, Kranjc K, Kocevar M, Kuncser V, Richards R. Appl. Catal. A-Gen., 2008, 346 (1/2): 28-35[64] Panella B, Vargas A, Baiker A. J. Catal., 2009, 261 (1): 88-93[65] Lee D, Lee J, Lee H, Jin S, Hyeon T, Kim B M. Adv. Synth. Catal., 2006, 348 (1/2): 41-46[66] Zheng X X, Luo S Z, Zhang L, Cheng J P. Green Chem., 2009, 11 (4): 455-458[67] Dálaigh C , Corr S A, Gun'ko Y, Connon S J. Angew. Chem., 2007, 119 (23): 4407-4410[68] Chen H T, Huh S, Wiench J W, Pruski M, Lin V S Y. J. Am. Chem. Soc., 2005, 127 (38): 13305-13311[69] Gill C S, Price B A, Jones C W. J. Catal., 2007, 251 (1): 145-152[70] Phan N T S, Jones C W. J. Mol. Catal. A Chem., 2006, 253 (1/2): 123-131[71] Bass J D, Anderson S L, Katz A. Angew. Chem., 2003, 115 (42): 5377-5380[72] Yoon H, Ko S, Jang J. Chem. Commun., 2007, (14): 1468-1470[73] Ko S, Jang J. Angew. Chem., 2006, 118 (45): 7726-7729[74] Tsang S C, Caps V, Paraskevas I, Chadwick D, Thompsett D. Angew. Chem., 2004, 116 (42): 5763-5767[75] Schätz A, Grass R N, Stark W J, Reiser O. Chem. Eur. J., 2008, 14 (27): 8262-8266[76] Stein M, Wieland J, Steurer P, Tölle F, Mülhaupt R, Breit B. Adv. Synth. Catal., 2011, 353 (4): 523-527[77] Lu A H, Schmidt W, Matoussevitch N, Bönnemann H, Spliethoff B, Tesche B, Bill E, Kiefer W, Schüth F. Angew. Chem., 2004, 116 (33): 4403-4406[78] Aschwanden L, Panella B, Rossbach P, Keller B, Baiker A. ChemCatChem, 2009, 1 (1): 111-115[79] Mori K, Kanai S, Hara T, Mizugaki T, Ebitani K, Jitsukawa K, Kaneda K. Chem. Mater., 2007, 19 (6): 1249-1256[80] Hara T, Kaneta T, Mori K, Mitsudome T, Mizugaki T, Ebitani K, Kaneda K. Green Chem., 2007, 9 (11): 1246-1251[81] Zhang Y, Zhao Y W, Xia C G. J. Mol. Catal. A Chem., 2009, 306 (1/2): 107-112[82] Kwon M S, Park I S, Jang J S, Lee J S, Park J. Org. Lett., 2007, 9 (17): 3417-3419 |
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