Mild method for ullmann coupling reaction of amines and aryl halides

Organic Letters

Volumn 5, Issue 14, 2003, Pages 2453-2455

  Ma, Dawei ^a   Cai, Qian ^a   Zhang, Hui ^b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b FUDAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; HALIDE; IODIDE; LIGAND; PROLINE; SARCOSINE;

AMINATION; ARTICLE; CHEMICAL REACTION; TEMPERATURE; ULLMANN COUPLING REACTION;

EID: 0141854366     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0346584     Document Type: Article

References (20)

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17. For other recent efforts on the development of more efficient catalytic systems for Ullmann-type aryl amination, see: (a) Gujadhur, R. K.; Bates, C. G. ; Venkataraman, D. Org. Lett. 2001, 3, 4315-4317. (b) Gujadhur, R. K.; Venkataraman, D.; Kintigh, J. T. Tetrahedron Lett. 2001, 42, 4791-4793. (c) Goodbrand, H. B.; Hu, N.-X. J. Org. Chem. 1999, 64, 670-674. (d) Kang, S.-K.; Kim, D.-H.; Park, J.-N. Synlett 2002, 427-430. (e) Kelkar, A. A.; Patil, N. M.; Chaudhari, R. V. Tetrahedron Lett. 2002, 43, 7143-7146.
18. For other recent efforts on the development of more efficient catalytic systems for Ullmann-type aryl amination, see: (a) Gujadhur, R. K.; Bates, C. G. ; Venkataraman, D. Org. Lett. 2001, 3, 4315-4317. (b) Gujadhur, R. K.; Venkataraman, D.; Kintigh, J. T. Tetrahedron Lett. 2001, 42, 4791-4793. (c) Goodbrand, H. B.; Hu, N.-X. J. Org. Chem. 1999, 64, 670-674. (d) Kang, S.-K.; Kim, D.-H.; Park, J.-N. Synlett 2002, 427-430. (e) Kelkar, A. A.; Patil, N. M.; Chaudhari, R. V. Tetrahedron Lett. 2002, 43, 7143-7146.
19. For other recent efforts on the development of more efficient catalytic systems for Ullmann-type aryl amination, see: (a) Gujadhur, R. K.; Bates, C. G. ; Venkataraman, D. Org. Lett. 2001, 3, 4315-4317. (b) Gujadhur, R. K.; Venkataraman, D.; Kintigh, J. T. Tetrahedron Lett. 2001, 42, 4791-4793. (c) Goodbrand, H. B.; Hu, N.-X. J. Org. Chem. 1999, 64, 670-674. (d) Kang, S.-K.; Kim, D.-H.; Park, J.-N. Synlett 2002, 427-430. (e) Kelkar, A. A.; Patil, N. M.; Chaudhari, R. V. Tetrahedron Lett. 2002, 43, 7143-7146.
20. For other recent efforts on the development of more efficient catalytic systems for Ullmann-type aryl amination, see: (a) Gujadhur, R. K.; Bates, C. G. ; Venkataraman, D. Org. Lett. 2001, 3, 4315-4317. (b) Gujadhur, R. K.; Venkataraman, D.; Kintigh, J. T. Tetrahedron Lett. 2001, 42, 4791-4793. (c) Goodbrand, H. B.; Hu, N.-X. J. Org. Chem. 1999, 64, 670-674. (d) Kang, S.-K.; Kim, D.-H.; Park, J.-N. Synlett 2002, 427-430. (e) Kelkar, A. A.; Patil, N. M.; Chaudhari, R. V. Tetrahedron Lett. 2002, 43, 7143-7146.