Recent Advances and Perspectives in the Copper‐Catalysed Amination of Aryl and Heteroaryl Halides

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[27]  Haoxiang Hu,et al.  Synthesis of N‐Arylamides by Copper‐Catalyzed Amination of Aryl Halides with Nitriles , 2013 .

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[32]  Carlo Adamo,et al.  Influence of the Formation of the Halogen Bond ArX- - -N on the Mechanism of Diketonate Ligated Copper-Catalyzed Amination of Aromatic Halides , 2012 .

[33]  Yatao Qiu,et al.  An efficient copper-catalyzed synthesis of anilines by employing aqueous ammonia. , 2011, Organic & biomolecular chemistry.

[34]  Yunyang Wei,et al.  A simple and efficient copper-catalyzed amination of aryl halides by aqueous ammonia in water , 2011 .

[35]  C. Bolm,et al.  Microwave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles , 2011 .

[36]  C. Bolm,et al.  Ligand-Free Copper-Catalyzed Amination of Heteroaryl Halides with Alkyl- and Arylamines , 2010 .

[37]  Jianwei Xie,et al.  Efficient Copper-Catalyzed Direct Amination of Aryl Halides Using Aqueous Ammonia in Water , 2010 .

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[39]  C. Ramana,et al.  The [Cu]-catalyzed SNAR reactions: direct amination of electron deficient aryl halides with sodium azide and the synthesis of arylthioethers under Cu(II)–ascorbate redox system , 2010 .

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[41]  R. Qiao,et al.  Copper-catalyzed direct amination of ortho-functionalized haloarenes with sodium azide as the amino source. , 2010, The Journal of organic chemistry.

[42]  L. Barré,et al.  Copper-catalyzed amination of (bromophenyl)ethanolamine for a concise synthesis of aniline-containing analogues of NMDA NR2B antagonist ifenprodil. , 2010, Organic & biomolecular chemistry.

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[44]  M. Taillefer,et al.  Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions. , 2009, Angewandte Chemie.

[45]  Deping Wang,et al.  An Efficient Copper-Catalyzed Amination of Aryl Halides by Aqueous Ammonia , 2009 .

[46]  S. Chankeshwara,et al.  Protic acid immobilized on solid support as an extremely efficient recyclable catalyst system for a direct and atom economical esterification of carboxylic acids with alcohols. , 2009, The Journal of organic chemistry.

[47]  K. Alimohammadi,et al.  Microwave-assisted chemoselective copper-catalyzed amination of o-chloro and o-bromobenzoic acids using aromatic amines under solvent free conditions , 2009 .

[48]  Wen-Jun Zhou,et al.  Pd(PPh3)4-PEG 400 catalyzed protocol for the atom-efficient Stille cross-coupling reaction of organotin with aryl bromides. , 2009, The Journal of organic chemistry.

[49]  Xiaohu Deng,et al.  CuI-catalyzed amination of arylhalides with guanidines or amidines: a facile synthesis of 1-H-2-substituted benzimidazoles. , 2009, The Journal of organic chemistry.

[50]  Limin Wang,et al.  Hemilabile-coordinated copper promoted amination of aryl halides with ammonia in aqueous ethylene glycol under atmosphere pressure , 2009 .

[51]  M. Taillefer,et al.  A very simple copper-catalyzed synthesis of anilines by employing aqueous ammonia. , 2009, Angewandte Chemie.

[52]  K. Okano,et al.  A mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAc , 2008 .

[53]  S. Buchwald,et al.  Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction. , 2008, Organic letters.

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[55]  S. Ji,et al.  Copper-catalyzed amination of aryl halides with nitrogen-containing heterocycle using hippuric acid as the new ligand , 2008 .

[56]  Q. Guo,et al.  Copper-catalyzed synthesis of primary arylamines from aryl halides and 2,2,2-trifluoroacetamide , 2008 .

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[59]  Yuyang Jiang,et al.  CuBr/rac-BINOL-catalyzed N-arylations of aliphatic amines at room temperature. , 2007, The Journal of organic chemistry.

[60]  D. Viña,et al.  Regioselective synthesis of 1-alkyl- or 1-aryl-1H-indazoles via copper-catalyzed cyclizations of 2-haloarylcarbonylic compounds. , 2007, Organic letters.

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[64]  C. Wolf,et al.  Regioselective copper-catalyzed amination of chlorobenzoic acids: synthesis and solid-state structures of N-aryl anthranilic acid derivatives. , 2006, The Journal of organic chemistry.

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