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Chemical Communications

Volumn , Issue 46, 2008, Pages 6200-6202

Cross-coupling of aryl/heteroaryl bromides with ammonia using a copper-carbene catalyst

(4) Ntaganda, Rukundo a Dhudshia, Bhartesh a Macdonald, Charles L B a Thadani, Avinash N a

a UNIVERSITY OF WINDSOR (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; BROMINE DERIVATIVE; CARBENE; COPPER; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; COMPLEX FORMATION; CROSS COUPLING REACTION; CRYSTAL STRUCTURE; REACTION ANALYSIS;

EID: 56849124018 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b815757j Document Type: Article

Times cited : (37)

References (40)

1
- 0003453969
- Wiley-VCH, Weinheim
- M. Appl, in Ammonia: Principles and Industrial Practice, Wiley-VCH, Weinheim, 1999
- (1999) Ammonia: Principles and Industrial Practice
- Appl In, M.¹

2
- 28744441905
- Cambridge University Press, Cambridge
- S. A. Lawrence, in Amines: Synthesis, Properties and Application, Cambridge University Press, Cambridge, 2004
- (2004) Amines: Synthesis, Properties and Application
- Lawrence In, S.A.¹

3
- 0003853725
- Akademie Verlag GmbH, Berlin, 7th ed.
- M. Negwer, in Organic Drugs and their Synonyms, Akademie Verlag GmbH, Berlin, 7th ed., 1994
- (1994) Organic Drugs and Their Synonyms
- Negwer In, M.¹

4
- 56849132835
- P. A. Lewis, John Wiley, New York
- Pigment Handbook, ed., P. A. Lewis,, John Wiley, New York, 1988
- (1988) Pigment Handbook, Ed.

5
- 12344337315
- B. Schlummer U. Scholz Adv. Synth. Catal. 2004 346 1599 1626
- (2004) Adv. Synth. Catal. , vol.346 , pp. 1599-1626
- Schlummer, B.¹ Scholz, U.²

6
- 28244465191
- B. Dhudshia J. Tiburcio A. N. Thadani Chem. Commun. 2005 5551 5553
- (2005) Chem. Commun. , pp. 5551-5553
- Dhudshia, B.¹ Tiburcio, J.² Thadani, A.N.³

7
- 50849143801
- For reviews on copper-catalyzed N-arylations, see:
- R. Ntaganda T. Milovic J. Tiburcio A. N. Thadani Chem. Commun. 2008 4052 4054
- (2008) Chem. Commun. , pp. 4052-4054
- Ntaganda, R.¹ Milovic, T.² Tiburcio, J.³ Thadani, A.N.⁴

8
- 0345708168
- S. V. Ley A. W. Thomas Angew. Chem., Int. Ed. 2003 42 5400 5449
- (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400-5449
- Ley, S.V.¹ Thomas, A.W.²

9
- 0346749657
- K. Kunz U. Scholz D. Ganzer Synlett 2003 2428 2439
- (2003) Synlett , pp. 2428-2439
- Kunz, K.¹ Scholz, U.² Ganzer, D.³

10
- 9644277114
- I. P. Beletskaya A. V. Cheprakov Coord. Chem. Rev. 2004 248 2337 2364
- (2004) Coord. Chem. Rev. , vol.248 , pp. 2337-2364
- Beletskaya, I.P.¹ Cheprakov, A.V.²

11
- 0036099296
- J. P. Finet A. Y. Fedorov S. Combes G. Boyer Curr. Org. Chem. 2002 6 597 626
- (2002) Curr. Org. Chem. , vol.6 , pp. 597-626
- Finet, J.P.¹ Fedorov, A.Y.² Combes, S.³ Boyer, G.⁴

12
- 34250694837
- S. R. Chemler P. H. Fuller Chem. Soc. Rev. 2007 36 1153 1160
- (2007) Chem. Soc. Rev. , vol.36 , pp. 1153-1160
- Chemler, S.R.¹ Fuller, P.H.²

13
- 47749142816
- F. Monnier M. Taillefer Angew. Chem., Int. Ed. 2008 47 3096 3099
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3096-3099
- Monnier, F.¹ Taillefer, M.²

14
- 41149131770
- For select recent examples of Cu-catalyzed N-arylations/alkenylations, see:
- M. Carril R. SanMartin E. Domínguez Chem. Soc. Rev. 2008 37 639 647
- (2008) Chem. Soc. Rev. , vol.37 , pp. 639-647
- Carril, M.¹ Sanmartin, R.² Domínguez, E.³

15
- 48249117090
- J. W. Tye Z. Weng A. M. Johns C. D. Incarvito J. F. Hartwig J. Am. Chem. Soc. 2008 130 9971 9983
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 9971-9983
- Tye, J.W.¹ Weng, Z.² Johns, A.M.³ Incarvito, C.D.⁴ Hartwig, J.F.⁵

16
- 51649124289
- A. Minatti S. L. Buchwald Org. Lett. 2008 10 2721 2724
- (2008) Org. Lett. , vol.10 , pp. 2721-2724
- Minatti, A.¹ Buchwald, S.L.²

17
- 47749112913
- R. A. Altman A. M. Hyde X. Huang S. L. Buchwald J. Am. Chem. Soc. 2008 130 9613 9620
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 9613-9620
- Altman, R.A.¹ Hyde, A.M.² Huang, X.³ Buchwald, S.L.⁴

18
- 53349121032
- C. He C. Chen J. Cheng C. Liu W. Liu Q. Li A. Lei Angew. Chem., Int. Ed. 2008 47 6414 6417
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 6414-6417
- He, C.¹ Chen, C.² Cheng, J.³ Liu, C.⁴ Liu, W.⁵ Li, Q.⁶ Lei, A.⁷

19
- 47749101331
- L. M. Huffman S. S. Stahl J. Am. Chem. Soc. 2008 130 9196 9197
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 9196-9197
- Huffman, L.M.¹ Stahl, S.S.²

20
- 52049112609
- Z. Zhang Y. Yu L. S. Liebeskind Org. Lett. 2008 10 3005 3008
- (2008) Org. Lett. , vol.10 , pp. 3005-3008
- Zhang, Z.¹ Yu, Y.² Liebeskind, L.S.³

21
- 40849094697
- C. Worch C. Bolm Synthesis 2008 739 742
- (2008) Synthesis , pp. 739-742
- Worch, C.¹ Bolm, C.²

22
- 41949133170
- Y. Bolshan R. A. Batey Angew. Chem., Int. Ed. 2008 47 2109 2112
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2109-2112
- Bolshan, Y.¹ Batey, R.A.²

23
- 46249084624
- J. Kim S. Chang Chem. Commun. 2008 3052 3054
- (2008) Chem. Commun. , pp. 3052-3054
- Kim, J.¹ Chang, S.²

24
- 0035821252
- For a recent review on the catalytic use of Cu-NHC complexes in organic synthesis, see:
- F. Lang D. Zewge I. N. Houpis R. P. Volante Tetrahedron Lett. 2001 42 3251 3254
- (2001) Tetrahedron Lett. , vol.42 , pp. 3251-3254
- Lang, F.¹ Zewge, D.² Houpis, I.N.³ Volante, R.P.⁴

25
- 51049119177
- and references therein For recent examples on the catalytic use of Cu-NHC complexes in organic synthesis, see:
- S. Díez-González S. P. Nolan Aldrichimica Acta 2008 41 43 51
- (2008) Aldrichimica Acta , vol.41 , pp. 43-51
- Díez-González, S.¹ Nolan, S.P.²

26
- 54749133762
- S. Díez-González E. D. Stevens S. P. Nolan Chem. Commun. 2008 4747
- (2008) Chem. Commun. , pp. 4747
- Díez-González, S.¹ Stevens, E.D.² Nolan, S.P.³

27
- 53549095988
- T. Ohishi M. Nishiura Z. Hou Angew. Chem., Int. Ed. 2008 47 5792 5795
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 5792-5795
- Ohishi, T.¹ Nishiura, M.² Hou, Z.³

28
- 39649095613
- O. Winkelmann C. Näther U. Lüning J. Organomet. Chem. 2008 693 923 932
- (2008) J. Organomet. Chem. , vol.693 , pp. 923-932
- Winkelmann, O.¹ Näther, C.² Lüning, U.³

29
- 38349116528
- For an example on the use of a Cu-NHC complex in cross-coupling of aryl halides and azoles, see:
- J. A. Bull M. G. Hutchings C. Luján P. Quayle Tetrahedron Lett. 2008 49 1352 1356
- (2008) Tetrahedron Lett. , vol.49 , pp. 1352-1356
- Bull, J.A.¹ Hutchings, M.G.² Luján, C.³ Quayle, P.⁴

30
- 41549169511
- C. Tubaro A. Biffis E. Scattolin M. Basato Tetrahedron 2008 64 4187 4195
- (2008) Tetrahedron , vol.64 , pp. 4187-4195
- Tubaro, C.¹ Biffis, A.² Scattolin, E.³ Basato, M.⁴

31
- 33746931578
- Q. Shen J. F. Hartwig J. Am. Chem. Soc. 2006 128 10028 10029
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 10028-10029
- Shen, Q.¹ Hartwig, J.F.²

32
- 34548249621
- For select examples of the use of ammonia surrogates in cross-coupling reactions, see:
- D. S. Surry S. L. Buchwald J. Am. Chem. Soc. 2007 129 10354 10355
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 10354-10355
- Surry, D.S.¹ Buchwald, S.L.²

33
- 0034712156
- J. P. Wolfe H. Tomori J. P. Sadighi J. J. Yin S. L. Buchwald J. Org. Chem. 2000 65 1158 1174
- (2000) J. Org. Chem. , vol.65 , pp. 1158-1174
- Wolfe, J.P.¹ Tomori, H.² Sadighi, J.P.³ Yin, J.J.⁴ Buchwald, S.L.⁵

34
- 0038579438
- X. H. Huang K. W. Anderson D. Zim L. Jiang A. Klapars S. L. Buchwald J. Am. Chem. Soc. 2003 125 6653 6655
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 6653-6655
- Huang, X.H.¹ Anderson, K.W.² Zim, D.³ Jiang, L.⁴ Klapars, A.⁵ Buchwald, S.L.⁶

35
- 0035900483
- G. A. Grasa M. S. Viciu J. K. Huang S. P. Nolan J. Org. Chem. 2001 66 7729 7737
- (2001) J. Org. Chem. , vol.66 , pp. 7729-7737
- Grasa, G.A.¹ Viciu, M.S.² Huang, J.K.³ Nolan, S.P.⁴

36
- 0347761333
- J. Barluenga F. Aznar C. Valdes Angew. Chem., Int. Ed. 2004 43 343 345
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 343-345
- Barluenga, J.¹ Aznar, F.² Valdes, C.³

37
- 0042704188
- S. Lee M. Jorgensen J. F. Hartwig Org. Lett. 2001 3 2729 2732
- (2001) Org. Lett. , vol.3 , pp. 2729-2732
- Lee, S.¹ Jorgensen, M.² Hartwig, J.F.³

38
- 18244392661
- 1H NMR of the crude reaction mixtures revealed <5% of product formation in all cases The structure of 2a is similar to the reported structures of 2b and 2c, see:
- D.-Y. Lee J. F. Hartwig Org. Lett. 2005 7 1169 1172
- (2005) Org. Lett. , vol.7 , pp. 1169-1172
- Lee, D.-Y.¹ Hartwig, J.F.²

39
- 54749133762
- S. Díez-González E. D. Stevens S. P. Nolan Chem. Commun. 2008 4747
- (2008) Chem. Commun. , pp. 4747
- Díez-González, S.¹ Stevens, E.D.² Nolan, S.P.³

40
- 56849084865
- ® reactor was ca. 100 psi
- S. Díez-González H. Kaur F. K. Zinn E. D. Stevens S. P. Nolan J. Org. Chem. 2005 70 4674 4796
- (2005) J. Org. Chem. , vol.70 , pp. 4674-4796
- Díez-González, S.¹ Kaur, H.² Zinn, F.K.³ Stevens, E.D.⁴ Nolan, S.P.⁵

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