Room temperature Stille cross-coupling reaction of unreactive aryl chlorides and heteroaryl chlorides

Chemical Communications

Volumn 46, Issue 3, 2010, Pages 478-480

  Lee, Dong Hwan ^a   Taher, Abu ^a   Ahn, Wha Seung ^a   Jin, Myung Jong ^a  

^a Inha University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; HETEROCYCLIC COMPOUND; IMINE; ORGANOTIN COMPOUND; PALLADIUM COMPLEX; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMPLEX FORMATION; REACTION ANALYSIS; ROOM TEMPERATURE; STILLE REACTION;

EID: 75649102765     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b917711f     Document Type: Article

References (32)

1. J. K. Stille Pure Appl. Chem. 1985 57 1771
2. M. Pereyre, J. P. Quintard and A. Rahm, Tin in Organic Synthesis, Butterworth, London, 1987
3. V. Farina, V. Krishnamurthy and W. J. Scott, The Stille Reaction, John Wiley & Sons, New York, NY, 1998
4. T. N. Mitchell, Metal-catalyzed Cross-coupling Reactions, Wiley-VCH, Weinheim, 2004
5. P. Espinet A. M. Echavarren Angew. Chem. Int. Ed. 2004 43 4704
6. G. Bringmann D. Menche Acc. Chem. Res. 2001 34 615
7. G. Bringmann Y. Reichert V. V. Kane Tetrahedron 2004 60 3539
8. T. W. Wallace Org. Biomol. Chem. 2006 4 3197
9. T. C. Roberts P. A. Smith R. T. Cirz R. E. Romesberg J. Am. Chem. Soc. 2007 129 15830
10. J.-H. Li Y. Liang D.-P. Wang W.-J. Liu Y.-X. Xie D.-L. Yin J. Org. Chem. 2005 70 2832
11. S. P. H. Mee V. Lee J. E. Baldwin Chem.-Eur. J. 2005 11 3294
12. J. Hämmerle M. Schnürch P. Stanetty Synlett. 2007 2975
13. W.-J. Zhou K.-H. Wang J.-X. Wang Adv. Synth. Catal. 2009 351 1378
14. V. V. Grushin and H. Alper, in Activation of Unreactive Bonds and Organic Synthesis, ed., S. Murai, Springer, Berlin, 1999
15. A. F. Littke G. C. Fu Angew. Chem., Int. Ed. 2002 41 4176
16. R. B. Bedford C. S. J. Cazin D. Holder Coord. Chem. Rev. 2004 248 2283
17. A. F. Littke L. Schwarz G. C. Fu J. Am. Chem. Soc. 2002 124 6343
18. C. Wolf R. Lerebours J. Org. Chem. 2003 68 7551
19. W. Su S. Urgaonkar A. Patrick McLaughlin G. Verkade J. Am. Chem. Soc. 2004 126 16433
20. J. R. Naber S. L. Buchwald Adv. Synth. Catal. 2008 350 957
21. S. Doherty R. J. Errington N. Housley J. Ridland W. Clegg M. R. J. Elsegood Organometallics 1999 18 1018
22. H. Hatem D. B. Isabelle M. Perrin R. Lamartine J. Org. Chem. 2004 69 6521
23. S. W. Lim J. C. Lee D. S. Shon W. I. Lee I. M. Lee Chem. Mater. 2002 14 1548
24. D. Zhang G. X. Jin N. Hu Chem. Commun. 2002 574
25. D.-H. Lee J.-Y. Jung I. M. Lee M.-J. Jin Eur. J. Org. Chem. 2008 356
26. D.-H. Lee H. Qiu M.-H. Cho I. M. Lee M.-J. Jin Synlett. 2008 1657
27. F. T. Ladipo G. K. Anderson Organometallics 1994 13 303
28. S.-L. Ku X.-P. Hui C.-A. Chen Y.-Y. Kuo H.-M. Gau Chem. Commun. 2007 3847
29. G. C. Fu Acc. Chem. Res. 2008 41 1555
30. A. F. Pozharskii, A. T. Spldartenko and A. Katritzky, Heterocycles in Life and Society, Wiley, New York, 1997
31. E. Tyrell P. Brookes Synthesis 2004 4 469
32. I. J. S. Fairlamb Chem. Soc. Rev. 2007 36 1036