OALib Journal期刊
ISSN: 2333-9721
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基于C-H键活化的铜催化二苄胺氧化酰胺化反应
DOI: 10.1016/S1872-2067(12)60617-2, PP. 1644-1650
Keywords: C-H键活化,铜催化剂,二乙酸碘苯,氧化酰基化,二苄胺
Abstract:
?基于铜催化的C-H键活化构建了一类高效的二苄胺氧化酰基化生成N-苄基苯甲酰胺的反应.该反应使用CuBr作为催化剂,二乙酸碘苯作为氧化剂,在温和条件下生成两种酰胺,总产率最高可达92.0%.CuBr催化剂价廉易得,催化活性高.同时这也是首次使用二乙酸碘苯作为氧化剂,通过二苄胺的直接氧化酰基化反应合成N-苄基苯甲酰胺.
References
[1] | Jursic B S, Zdravkovski Z. Synth Commun, 1993, 23: 2761
|
[2] | Montalbetti C A G N, Falque V. Tetrahedron, 2005, 61: 10827
|
[3] | Valeur E, Bradley M. Chem Soc Rev, 2009, 38: 606
|
[4] | Allen C L, Williams J M J. Chem Soc Rev, 2011, 40: 3405
|
[5] | Nordstr?m L U, Vogt H, Madsen R. J Am Chem Soc, 2008, 130: 17672
|
[6] | Chang J W W, Chan P W H. Angew Chem, Int Ed, 2008, 47: 1138
|
[7] | Ghosh S C, Muthaiah S, Zhang Y, Xu X Y, Hong S H. Adv Synth Catal, 2009, 351: 2643
|
[8] | Li G L, Kung K K Y, Wong M K. Chem Commun, 2012, 48: 4112
|
[9] | Cui Y, He C. Angew Chem, Int Ed, 2004, 43: 4210
|
[10] | Miriyala B, Bhattacharyya S, Williamson J S. Tetrahedron, 2004, 60: 1463
|
[11] | Pattabiraman V R, Bode J W. Nature, 2011, 480: 471
|
[12] | Zhang J, Hong S H. Org Lett, 2012, 14: 4646
|
[13] | Yoo W J, Li C J. J Am Chem Soc, 2006, 128: 13064
|
[14] | Li Y M, Jia F, Li Z P. Chem Eur J, 2013, 19: 82
|
[15] | Fang C, Qian W X, Bao W L. Synlett, 2008: 2529
|
[16] | De Sarkar S, Studer A. Org Lett, 2010, 12: 1992
|
[17] | Brennführer A, Neumann H, Beller M. Angew Chem, Int Ed, 2009, 48: 4114
|
[18] | Eldred S E, Stone D A, Gellman S H, Stahl S S. J Am Chem Soc, 2003, 125: 3422
|
[19] | Hoerter J M, Otte K M, Gellman S H, Stahl S S. J Am Chem Soc, 2006, 128: 5177
|
[20] | Allen C L, Atkinson B N, Williams J M J. Angew Chem, Int Ed, 2012, 51: 1383
|
[21] | Dineen T A, Zajac M A, Myers A G. J Am Chem Soc, 2006, 128: 16406
|
[22] | Burrows E P, Rosenblatt D H. J Org Chem, 1982, 47: 892
|
[23] | An G-i, Rhee H. Synlett, 2003: 876
|
[24] | Mohamed M A, Yamada K-i, Tomioka K. Tetrahedron Lett, 2009, 50: 3436
|
[25] | Guo S M, Qian B, Xie Y J, Xia C G, Huang H M. Org Lett, 2011, 13: 522
|
[26] | Tohma H, Takizawa S, Maegawa T, Kita Y. Angew Chem, Int Ed, 2000, 39: 1306
|
[27] | Espino C G, Wehn P M, Chow J, Du Bois J. J Am Chem Soc, 2001, 123: 6935
|
[28] | Liang J L, Yuan S X, Huang J S, Yu W Y, Che C M. Angew Chem, Int Ed, 2002, 41: 3465
|
[29] | Porta F, Crotti C, Cenini S, Palmisano G. J Mol Catal, 1989, 50: 333
|
[30] | Larsen J, J?rgensen K A. J Chem Soc, Perkin Trans 2, 1992: 1213
|
[31] | Moriarty R M, Gupta S C, Hu H, Berenschot D R, White K B. J Am Chem Soc, 1981, 103: 686
|
[32] | Oliveros E, Riviere M, Malrieu J P, Teichteil C. J Am Chem Soc, 1979, 101: 318
|
[33] | Gao J, Wang G W. J Org Chem, 2008, 73: 2955
|
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