Reaction of organozinc halides with aryl isocyanates

Tetrahedron

Volumn 69, Issue 12, 2013, Pages 2588-2593

  Yang, Haoran ^a   Huang, Danfeng ^a   Wang, Ke Hu ^a   Xu, Changming ^a   Niu, Teng ^a   Hu, Yulai ^a,b  

^a NORTHWEST NORMAL UNIVERSITY   (China)

^b LANZHOU UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; HALIDE; ISOCYANIC ACID DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CRYSTAL STRUCTURE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 84874107472     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.01.053     Document Type: Article

References (49)

1. P. Knochel, M.C.P. Yeh, S.C. Berk, and J. Talbert J. Org. Chem. 53 1988 2390 2392
2. M. Chen, X. Zheng, W. Li, J. He, and A. Lei J. Am. Chem. Soc. 132 2010 4101 4103
3. B.A. Haag, Z.-G. Zhang, J.-S. Li, and P. Knochel Angew. Chem., Int. Ed. 49 2010 9513 9516
4. M.R. Luzung, J.S. Patel, and J. Yin J. Org. Chem. 75 2010 8330 8332
5. G. Manolikakes, C.M. Hernandez, M.A. Schade, A. Metzger, and P. Knochel J. Org. Chem. 73 2008 8422 8436
6. C.S. Yeung, and V.M. Dong J. Am. Chem. Soc. 130 2008 7826 7827
7. P. Knochel Handbook of Functionalized Organometallics 2005 Wiley-VCH Weinhein, Germany
8. A. Leprêtre, A. Turck, N. Plé, P. Knochel, and G. Quéguiner Tetrahedron 56 2000 265 274
9. P. Knochel, and R.D. Singer Chem. Rev. 93 1993 2117 2188
10. E. Erdik Tetrahedron 48 1992 9577 9648
11. P. Knochel, J.J. Almena Perea, and P. Jones Tetrahedron 54 1998 8275 8317
12. K.B. Urkalan, and M.S. Sigman J. Am. Chem. Soc. 131 2009 18042 18043
13. N. Hadei, G.T. Achondul, C. Valente, C.J. O'Brien, and M.G. Organ Angew. Chem., Int. Ed. 50 2011 3896 3899
14. A. Metzger, L. Melzig, C. Despotopoulou, and P. Knochel Org. Lett. 11 2009 4228 4231
15. N. Hadei, E.A.B. Kantchev, C.J. O'Brien, and M.G. Organ J. Org. Chem. 70 2005 8503 8507
16. X. Zeng, M. Qian, Q. Hu, and E. Negishi Angew. Chem., Int. Ed. 43 2004 2259 2263
17. E. Negishi Acc. Chem. Res. 15 1982 340 348
18. M. Li, X.-X. Yan, W. Hong, X.-Z. Zhu, B.-X. Cao, J. Sun, and X.-L. Hou Org. Lett. 6 2004 2833 2835
19. D. Wang, and Z. Zhang Org. Lett. 5 2003 4645 4648
20. L. Melzig, A. Metzger, and P. Knochel J. Org. Chem. 75 2010 2131 2133
21. L.-G. Xie, and Z.-X. Wang Angew. Chem., Int. Ed. 50 2011 4901 4904
22. B.-J. Li, Y.-Z. Li, X.-Y. Lu, J. Liu, B.-T. Guan, and Z.-J. Shi Angew. Chem., Int. Ed. 47 2008 10124 10127
23. C. Fischer, and G.C. Fu J. Am. Chem. Soc. 127 2005 4594 4595
24. V.B. Phapale, E. Buñuel, M. García-Iglesias, and D.J. Cárdenas Angew. Chem., Int. Ed. 46 2007 8790 8795
25. A. Gavryushin, C. Kofink, G. Manolikakes, and P. Knochel Org. Lett. 7 2005 4871 4874
26. H. Ochiai, M. Jang, K. Hirano, H. Yorimitsu, and K. Oshima Org. Lett. 10 2008 2681 2683
27. J. Esquivias, R.G. Arráyas, and J.C. Carretero Angew. Chem., Int. Ed. 46 2007 9257 9260
28. M.C.P. Yeh, and P. Knochel Tetrahedron Lett. 30 1989 4799 4802
29. M.C.P. Yeh, P. Knochel, and L.E. Santa Tetrahedron Lett. 29 1988 3887 3890
30. C.K. Reddy, and P. Knochel Angew. Chem., Int. Ed. 35 1996 1700 1701
31. I. Kazmierski, M. Bastienne, C. Gosmini, J.-M. Paris, and J. Périchon J. Org. Chem. 69 2004 936 942
32. H. Fillon, C. Gosmini, and J. Perichon J. Am. Chem. Soc. 125 2003 3867 3870
33. C. Gosmini, Y. Rollin, J.Y. Nedelec, and J. Perichon J. Org. Chem. 65 2000 6024 6026
34. Z.-Y. Peng, F.-F. Ma, L.-F. Zhu, X.-M. Xie, and Z. Zhang J. Org. Chem. 74 2009 6855 6858
35. A. Metzger, S. Bernhardt, G. Manolikakes, and P. Knochel Angew. Chem., Int. Ed. 49 2010 4665 4668
36. K. Kobayashi, and Y. Kondo Org. Lett. 11 2009 2035 2037
37. A. Zakarian, A. Batch, and R.A. Holton J. Am. Chem. Soc. 125 2003 7822 7824
38. I. Kadota, H. Takamura, K. Sato, and Y. Yamamoto J. Org. Chem. 67 2002 3494 3498
39. Q. Dai, X. Xie, S. Xu, D. Ma, S. Tang, and X. She Org. Lett. 13 2011 2302 2305
40. S.K. Pandey, and C.V. Ramana J. Org. Chem. 76 2011 2315 2318
41. A.F. Petri, J.S. Schneekloth, A.K. Mandal, and C.M. Crews Org. Lett. 9 2007 3001 3004
42. J.-X. Wang, Y. Fu, and Y. Hu Angew. Chem., Int. Ed. 41 2002 2757 2760
43. Y. Hu, J. Yu, S. Yang, J.-X. Wang, and Y. Yin Synlett 1998 1213 1214
44. Y. Hu, J.-X. Wang, and W. Li Chem. Lett. 2001 174 175
45. J.-X. Wang, Y. Fu, Y. Hu, and K. Wang Synthesis 2003 1506 1510
46. Y.-J. Wei, H. Ren, and J.-X. Wang Tetrahedron Lett. 49 2008 5697 5699
47. J.-X. Wang, K. Wang, L. Zhao, H. Li, Y. Fu, and Y. Hu Adv. Synth. Catal. 348 2006 1262 1270
48. D. Huang, and J.-X. Wang Synlett 2007 2272 2276
49. Y. Fu, J.-X. Wang, K. Wang, and Y. Hu Tetrahedron 64 2008 11124 11128