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Volumn 10, Issue 11, 2012, Pages 2206-2208

Well-defined (N-heterocyclic carbene)-Ag(i) complexes as catalysts for A 3 reactions

Author keywords

[No Author keywords available]

Indexed keywords

AG COMPLEX; N-HETEROCYCLIC CARBENES; ROOM TEMPERATURE; SHORT REACTION TIME;

ALDEHYDES; CARBON INORGANIC COMPOUNDS;

ORGANIC COMPOUNDS;

EID: 84863116804 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c2ob06900h Document Type: Article

Times cited : (64)

References (19)

1
- 0035796754
- S. Sakaguchi T. Kubo Y. Ishii Angew. Chem., Int. Ed. 2001 40 2534
- (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2534
- Sakaguchi, S.¹ Kubo, T.² Ishii, Y.³

2
- 0001751065
- C. Fisher E. M. Carreira Org. Lett. 2001 3 4319
- (2001) Org. Lett. , vol.3 , pp. 4319
- Fisher, C.¹ Carreira, E.M.²

3
- 0037034081
- C.-J. Li C. Wei Chem. Commun. 2002 268
- (2002) Chem. Commun. , pp. 268
- Li, C.-J.¹ Wei, C.²

4
- 4244076867
- T. Naota H. Takaya S. I. Murahashi Chem. Rev. 1998 98 2599
- (1998) Chem. Rev. , vol.98 , pp. 2599
- Naota, T.¹ Takaya, H.² Murahashi, S.I.³

5
- 0033553817
- G. Dyker Angew. Chem., Int. Ed. 1999 38 1698
- (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 1698
- Dyker, G.¹

6
- 0034609689
- For a very recent review, see
- G. S. Kauffman G. D. Harris R. L. Dorow B. R. P. Stone R. L. Parsons Jr. J. A. Pesti N. A. Magnus J. M. Fortunak P. N. Confalone W. A. Nugent Org. Lett. 2000 2 3119
- (2000) Org. Lett. , vol.2 , pp. 3119
- Kauffman, G.S.¹ Harris, G.D.² Dorow, R.L.³ Stone, B.R.P.⁴ Parsons, Jr.R.L.⁵ Pesti, J.A.⁶ Magnus, N.A.⁷ Fortunak, J.M.⁸ Confalone, P.N.⁹ Nugent, W.A.¹⁰

7
- 80052367835
- W.-J. Yoo L. Zhao C.-J. Li Aldrichimica Acta 2011 44 43
- (2011) Aldrichimica Acta , vol.44 , pp. 43
- Yoo, W.-J.¹ Zhao, L.² Li, C.-J.³

8
- 0344496729
- C. Wei Z. Li C.-J. Li Org. Lett. 2003 5 4473
- (2003) Org. Lett. , vol.5 , pp. 4473
- Wei, C.¹ Li, Z.² Li, C.-J.³

9
- 26444461420
- In that report there is one reaction carried out at room temperature involving the coupling of p-trifluoromethylbenzaldehyde and phenylacetylene, and using twice as much catalyst loading (10 mol%)
- X. Yao C.-J. Li Org. Lett. 2005 7 4395
- (2005) Org. Lett. , vol.7 , pp. 4395
- Yao, X.¹ Li, C.-J.²

10
- 78650638905
- ed., Springer, London
- Heterocyclic Carbenes in Transition Metals Catalysis and Organocatalysis, ed., C. S. J. Cazin, Springer, London, 2010
- (2010) Heterocyclic Carbenes in Transition Metals Catalysis and Organocatalysis
- Cazin, C.S.J.¹

11
- 33745688099
- ed., Springer, Berlin
- N-Heterocyclic Carbenes in Transition Metal Catalysis, ed., F. Glorius, Springer, Berlin, 2007
- (2007) N-Heterocyclic Carbenes in Transition Metal Catalysis
- Glorius, F.¹

12
- 79951632149
- Y. Li X. Chen Y. Song L. Fang G. Zou Dalton Trans. 2011 40 2046
- (2011) Dalton Trans. , vol.40 , pp. 2046
- Li, Y.¹ Chen, X.² Song, Y.³ Fang, L.⁴ Zou, G.⁵

13
- 53149119871
- P. Li L. Wang Y. Zhang M. Wang Tetrahedron Lett. 2008 49 6650
- (2008) Tetrahedron Lett. , vol.49 , pp. 6650
- Li, P.¹ Wang, L.² Zhang, Y.³ Wang, M.⁴

14
- 0344089067
- T. Ramnial C. D. Abernethy M. D. Spicer I. D. McKenzie I. D. Gay J. A. C. Clyburne Inorg. Chem. 2003 42 1391
- (2003) Inorg. Chem. , vol.42 , pp. 1391
- Ramnial, T.¹ Abernethy, C.D.² Spicer, M.D.³ McKenzie, I.D.⁴ Gay, I.D.⁵ Clyburne, J.A.C.⁶

15
- 30344459392
- P. de Frémont N. M. Scott E. D. Stevens T. Ramnial O. C. Lightbody C. L. B. Macdonald J. A. C. Clyburne C. D. Abernethy S. P. Nolan Organometallics 2005 24 6301
- (2005) Organometallics , vol.24 , pp. 6301
- De Frémont, P.¹ Scott, N.M.² Stevens, E.D.³ Ramnial, T.⁴ Lightbody, O.C.⁵ MacDonald, C.L.B.⁶ Clyburne, J.A.C.⁷ Abernethy, C.D.⁸ Nolan, S.P.⁹

16
- 70349780673
- D. Partyka N. Deligonul Inorg. Chem. 2009 48 9463
- (2009) Inorg. Chem. , vol.48 , pp. 9463
- Partyka, D.¹ Deligonul, N.²

17
- 61849089040
- D. V. Partyka T. J. Robilotto J. B. Updegraff III M. Zeller A. D. Hunter T. G. Gray Organometallics 2009 28 795
- (2009) Organometallics , vol.28 , pp. 795
- Partyka, D.V.¹ Robilotto, T.J.² Updegraff Iii, J.B.³ Zeller, M.⁴ Hunter, A.D.⁵ Gray, T.G.⁶

18
- 77951933689
- To the best of our knowledge there are not any reported crystal structures of (NHC)Ag(OAc) complexes, which would allow us to make a true comparison with the halide-bearing counterparts to explain the higher reactivity of 6. The crystal structure of the analogous (SIPr)Cu(OAc) suggests a more accessible metal centre when compared to (SIPr)CuCl
- C. A. Citadelle E. L. Nouy F. Bisaro A. M. Z. Slawin C. S. J. Cazin Dalton Trans. 2010 39 4489
- (2010) Dalton Trans. , vol.39 , pp. 4489
- Citadelle, C.A.¹ Nouy, E.L.² Bisaro, F.³ Slawin, A.M.Z.⁴ Cazin, C.S.J.⁵

19
- 33748291815
- L. A. Goj E. D. Blue S. A. Delp T. B. Gunnoe T. R. Cundari J. L. Petersen Organometallics 2006 25 4097
- (2006) Organometallics , vol.25 , pp. 4097
- Goj, L.A.¹ Blue, E.D.² Delp, S.A.³ Gunnoe, T.B.⁴ Cundari, T.R.⁵ Petersen, J.L.⁶

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