Erratum: Application of tautomerism of ferrocenyl secondary phosphine oxides in Suzuki - Miyaura cross coupling reactions (Organometallics (2009) 28 (6044) DOI: 10.1021/om900435y);Application of tautomerism of ferrocenyl secondary phosphine oxides in Suzuki-Miyaura cross-coupling reactions

Organometallics

Volumn 28, Issue 20, 2009, Pages 6044-6053

  Jung, Lin Ying ^a   Tsai, Shih Hung ^a   Hong, Fung E ^a  

^a NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; DIMERS; IRON COMPOUNDS; ORGANOMETALLICS; PHOSPHORUS COMPOUNDS; SINGLE CRYSTALS; X RAY DIFFRACTION;

ISOMERIC FORMS; PALLADIUM ACETATE; PALLADIUM-CATALYZED; SECONDARY PHOSPHINES; SINGLE CRYSTAL X-RAY DIFFRACTION METHOD; SUZUKI-MIYAURA CROSS-COUPLING REACTION; SUZUKI-MIYAURA REACTION; TAUTOMERIC EQUILIBRIA;

PALLADIUM COMPOUNDS;

EID: 70350291405     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9009685     Document Type: Erratum

References (54)

1. (a) Albenco, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007,107, 174-238.
2. (b) Coibet, J.-P.; Mignani, G. Chem, Rev. 2006,106,2651-2710.
3. (c) Hassan, J.; Sévingnon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Chem. Rev. 2002,102,1359-1469.
4. (d) Houk, K. N.; Sessler, H.; Lehn, J.-M.; Ley, S. V.; de Meijere, A.; Schreiber, S. L.; Thiem, J.; Trost, B. M.; Vögtle, F.; Yamamoto, H., Eds. Cross-Coupling Reactions-A Practical Guide in Topics in Current Chemistry; Springer-Verlag: Heidelberg, 2002; Vol. 219.
5. (a) Espinet, P.; Echavarren, A. M. Angew. Chem., Int. Ed, 2004, 43,4704-4734.
6. (b) Littke, A. F.;Fu, G. C. Angew. Chem., Int. Ed. 2002,41, 4176-4211.
7. (c) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95,2457-2483.
8. (a) Over 470 boronic acids and their derivatives are listed in the Alfa Äesar brochure Boronic Acids-Properties and Applications; Alfa Aesar: Germany, 2008.
9. (b) Hall, D. G., Ed. Boronic Acids; Wiley-VCH: Weinheim, 2005.
10. (c) Chemler, S. R.; Trauner, D.; Danishefsky, S. J. Angew. Chem., Int. Ed. 2001, 40, 4544-4568.
11. (d) Tsuji, J. Palladium. Reagents and Catalysts: New Perspectives for the 21st Century; John Wiley & Sons Ltd: England, 2004.
12. (a) Dixon, K. R.; Rattray, A. D. Can. J. Chem. 1971, 49, 3997-4004.
13. (b) Silver, B.; Luz, Z. J. Am. Chem. Soc. 1962, 84, 1091-1905.
14. (c) Luz, Z.; Silver,B. J. Am. Chem. Soc. 1962,84,1095-1098.
15. (d) Doak, G. O.; Freedman, L. D. Chem. Rev. 1961,61, 31-44.
16. (e) Luz, Z.; Silver, B. J. Am. Chem. Soc. 1961, 83, 4518-4521.
17. (a) Yang, D. X.; Colletti, S. L.; Wu, K.; Song, M.; Li, G. Y.; Shen, H. C. Org. Lett. 2009, 11, 381-384.
18. (b) Pryjomska, I.; Bechowski, H. B.; Ciunik, Z.; Trzeciak, A. M.; Ziólkowski, J. J. Dalton Trans. 2006,213-220.
19. (c) Ackennann, L.; Bom, R.; Spatz, J. H.; Meyer, D. Angew. Chem. 2005, 117, 7382-7386.
20. Angew. Chem., Int. Ed. 2005, 44, 7216-7219.
21. (d) Ackermann, L.; Born, R. Angew. Chem. 2005, 117, 2497-2500.
22. Angew. Chem., Int. Ed. 2005,44,2444-2447.
23. (e) Wolf, C.; Lerebours, R. Org. Lett. 2004,6,1147-11.50.
24. (f) Li, G. Y. J. Org. Chem. 2002,67,3643-3650.
25. (g)Li, G. Y. Angew. Chem, 2001,113,1561-1564.
26. Angew. Chem., Int. Ed. 2001, 40,1513-1516.
27. (h) Li, G. Y.; Zheng, G.; Noonan, A. F. J. Org. Chem. 2001, 66,8677-8681.
28. (a) Xu, H.; Ekoue-Kovi, K.; Wolf, C. J. Org. Chem. 2008, 73, 7638-7650.
29. (b) Ekoue-Kovi, K.; Xu, H.; Wolf, C. Tetrahedron Lett. 2008, 49, 5773-5776.
30. (c) Wei, C.-H.; Wu, C.-E.; Huang, Y.-L.; Kultyshev, R. G.; Hong, F.-E. Chem-Eur. J. 2007, 1.3, 1583-1593.
31. (d) Ackermann, L. Synlett 2007, 507-526.
32. (e) Ackermann, L. Synthesis 2006, 1557-1574.
33. (f) Ackermann, L.; Gschrei, C J.; Althammer, A.; Riederer, M. Chem. Commun. 2006, 1419-1421.
34. (g) Wolf, C.; Ekoue-Kovi, K. Eur. J. Org. Chem. 2006, 1917-1925.
35. (a) Baba, G.; Pilard, J.-F.; Tantaoul, K.; Gaumont, A.-C.; Denis, J.-M. Tetrahedron Lett. 1995, 36, 4421-4424.
36. (b) Pilard, J.-.F.; Baba, G.; Gaumont, A.-C.; Denis, J.-M. Synlett 1995, 1168-1170.
37. Intramolecular hydrogen bonding of related cases: (a) Wolf, C.; Lerebours, R. Org. Lett. 2004, 6, 1147-1150.
38. (b) Cobley, C. J.; van den Heuvel, M.; Abbadi, A.; de Vries, J. G. Tetrahedron Lett. 2000, 4.1,2467-2470.
39. 6a.
40. Amoroso, D.; Bell, A.; Protasiewicz, J. D. Organometallics 2005, 24,4099-4102.
41. (a) Goldman, E. R.; Medintz, I. L.; Whitley, J. L.; Hayhurst, A.; Clapp, A. R.; Uyeda, H. T.; Deschamps, J. R.; Lassman, M. E.; Mattoussi, H. J. Am. Chem. Soc 2005, 127, 6744-675.1.
42. (b) Braga, A. A. C.; Morgón, N. H.; Ujaque, G.; Maseras, F. J. Am. Chem. Soc. 2005,127, 9298-9307.
43. (a) Amatore, C.; Jutand, A. Acc. Chem. Res. 2000,33, 314-321.
44. (b) Amatare, C.; Carré, E.; Jutand, A.; M'Barki, M. A.; Meyer, G. Organometallics 1995,14,5605-5614.
45. (a) Dubbaka, S. R.; Vogel, P. Org. Lett. 2004, 6, 95-98.
46. (b) Grasa, G. A.; Hillier, A.C.; Nolan, S. P. Org. Lett. 2001, 3, 1077-1080.
47. (c) Miyaura, N.; Yamada, K.; Suginome, H.; Suzuki, A. J. Am. Chem. Soc. 1985, 107, 972-980.
48. Kataoka, N.; Shelby, Q.; Stambuli, J. P.; Hartwig, J. F. J. Org. Chem. 2002, 67, 5553-5566.
49. (a) Singh, R.; Viciu, M. S.; Kramareva, N.; Navarro, O.; Nolan, S. P. Org. Lett. 2005, 7, 1829-1832.
50. (b) Limmert, M. E.; Roy, A. H.; Hartwig, J. F. J. Org. Chem. 2005, 70,9364-9370.
51. (c) Xiong, Z.; Wang,N.; Dai, M.; Li, A.; Chen, J.; Yang, Z. Org. Lett. 2004,6,95-98.
52. (d) Dai, C.; Fu, G. C J. Am. Chem. Soc. 2001, 123, 2719-2724.
53. Sheldrick, G. M. SHELXTL PLUS User's Manual,.Revision4.1 ; Nicolet XRD Corporation: Madison, WI, 1991.
54. The hydrogen atoms were riding on carbons or oxygens, in their idealized positions and held fixed with C-H distances of 0.96 Å.