Ruthenium-catalysed carbenoid cyclopropanation reactions with diazo compounds

Chemical Society Reviews

Volumn 33, Issue 3, 2004, Pages 183-190

  Maas, Gerhard ^a  

^a UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; AZO COMPOUND; CARBENOID; LIGAND; ORGANIC COMPOUND; RUTHENIUM DERIVATIVE; STYRENE;

CATALYSIS; CATALYST; COMPLEX FORMATION; CYCLOPROPANATION; ENANTIOSELECTIVITY; MODEL; REVIEW;

EID: 2342522127     PISSN: 03060012     EISSN: 14604744     Source Type: Journal    
DOI: 10.1039/b309046a     Document Type: Article

References (52)

1. M. P. Doyle, M. A. McKervey and T. Ye, Modern Catalytic Methods for Organic Synthesis with Diazo Compounds, John Wiley & Sons, New York, 1998
2. M. P. Doyle, M. Protopopova, Tetrahedron, 1998, 54, 7919
3. E. A. Seddon and K. R. Seddon, The Chemistry of Ruthenium, Elsevier, Amsterdam, 1984
4. A. J. Anciaux, A. J. Hubert, A. F. Noels, N. Petiniot, P. Teyssié, J. Org. Chem., 1980, 45, 695
5. W. H. Tamblyn, S. R. Hoffmann, M. P. Doyle, J. Organomet. Chem., 1981, 216, C64
6. A. Demonceau, E. Saive, Y. de Froidmont, A. F. Noels, A. J. Hubert, I. T. Chizhevsky, I. A. Lobanova, V. I. Bregadze, Tetrahedron Lett., 1992, 33, 2009
7. A. Demonceau, A. F. Noels, E. Saive, A. J. Hubert, J. Mol. Catal., 1992, 76, 123
8. A. F. Noels, A. Demonceau, J. Phys. Org. Chem., 1998, 11, 602
9. A. F. Noels, A. Demonceau, D. Jan, Russ. Chem. Bull., 1999, 48, 1206
10. G. Maas, T. Werle, M. Alt, D. Mayer, Tetrahedron, 1993, 49, 881
11. T. Werle, G. Maas, Adv. Synth. Catal., 2001, 343, 37
12. G. Maas, J. Seitz, Tetrahedron Lett., 2001, 42, 6137
13. G. Maas, M. Alt, D. Mayer, U. Bergsträsser, S. Sklenak, P. Xavier, Y. Apeloig, Organometallics, 2001, 20, 4607
14. A. Demonceau, E. Abreu Dias, C. A. Lemoine, A. W. Stumpf, A. F. Noels, C. Pietraszuk, J. Gulinski, B. Marciniec, Tetrahedron Lett., 1995, 36, 3519
15. H. M. Lee, C. Bianchini, G. Jia, P. Barbaro, Organometallics, 1999, 18, 1961
16. A. Demonceau, F. Simal, A. F. Noels, C. Viñas, R. Nuñez, F. Teixidor, Tetrahedron Lett., 1997, 38, 4079
17. R. M. Stoop, C. Bauer, P. Setz, M. Wörle, T. Y. H. Wong, A. Mezzetti, Organometallics, 1999, 18, 5691
18. N. E. Leadbeater, K. A. Scott, L. J. Scott, J. Org. Chem., 2000, 65, 3231
19. F. Simal, D. Jan, A. Demonceau, A. F. Noels, Tetrahedron Lett., 1999, 40, 1653
20. F. Simal, A. Demonceau, A. F. Noels, Tetrahedron Lett., 1998, 39, 3493
21. W. Baratta, W. A. Herrmann, R. M. Kratzer, P. Rigi, Organometallics, 2000, 19, 3664
22. F. Simal, A. Demonceau, A. F. Noels, D. R. T. Knowles, S. O'Leary, P. M. Maitlis, O. Gusev, J. Organomet. Chem., 1998, 558, 163
23. H. Nishiyama, Y. Itoh, Y. Sugawara, H. Matsumoto, K. Aoki, K. Itoh, Bull. Chem. Soc. Jpn., 1995, 68, 1247
24. J. H. Simpson, J. Godfrey, R. Fox, A. Kotnis, D. Kacsur, J. Hamm, M. Totelben, V. Rosso, R. Mueller, E. Delaney, R. P. Deshpande, Tetrahedron: Asymmetry, 2003, 14, 3569
25. S. Iwasa, S. Tsushima, K. Nishiyama, Y. Tsuchiya, F. Takezawa, H. Nishiyama, Tetrahedron: Asymmetry., 2003, 14, 855
26. S.-B. Park, M. Sakata, H. Nishiyama, Chem. Eur. J., 1996, 2, 303.
27. H. Nishiyama, K. Aoki, H. Itoh, T. Iwamura, N. Sakata, O. Kurihara, Y. Motoyama, Chem. Lett., 1996, 1071
28. H. Nishiyama, N. Soeda, T. Naito, Y. Motoyama, Tetrahedron: Asymmetry, 1998, 9, 2865
29. C. Bianchini, H. M. Lee, Organometallics, 2000, 19, 1833
30. G. Chelucci, A. Saba, D. Vignola, C. Solinas, Tetrahedron, 2001, 57, 1099
31. S.-W. Park, J.-H. Son, S.-G. Kim, K. H. Ahn, Tetrahedron: Asymmetry, 1999, 10, 1903
32. T. Ushida, R. Irie, T. Katsuki, Tetrahedron, 2000, 56, 3501
33. T. Ushida, R. Irie, T. Katsuki, Synlett, 1999, 1793
34. T. Ushida, R. Irie, T. Katsuki, Synlett, 1999, 1163
35. X. Yao, M. Qiu, W. Lü, H. Chen, Z. Zheng, Tetrahedron: Asymmetry, 2001, 12, 197
36. Z. Zheng, X. Yao, C. Li, H. Chen, X. Hu, Tetrahedron Lett., 2001, 42, 2847
37. I. J. Munslow, K. M. Gillespie, R. J. Deeth, P. Scott, Chem. Commun., 2001, 1638
38. E. Galardon, P. Le Maux, G. Simonneaux, Chem. Commun., 1997, 927
39. E. Galardon, P. Le Maux, G. Simonneaux, Tetrahedron, 2000, 56, 615
40. W. C. Lo, C.-M. Che, K.-F. Cheng, T. C. W. Mak, Chem. Commun., 1997, 1205
41. M. Frauenkron, A. Berkessel, Tetrahedron Lett., 1997, 38, 7175
42. C.-M. Che, J. S. Huang, F.-W. Lee, Y. Li, T.-S. Lai, H.-L. Kwong, P.-F. Teng, W.-S. Lee, W.-C. Lo, S. M. Peng, Z.-Y. Zhou, J. Am. Chem. Soc., 2001, 123, 4119
43. J.-L. Zhang, H.-B. Zhou, J.-S. Huang, C.-M. Che, Chem. Eur. J., 2002, 8, 1554
44. E. Galardon, S. Roué, P. Le Maux, G. Simonneaux, Tetrahedron Lett., 1998, 39, 2333
45. J.-L. Zhang, C.-M. Che, Org. Lett., 2002, 4, 1911
46. J.-L. Zhang, Y.-L. Liu, C.-M. Che, Chem. Commun., 2002, 2906
47. S.-B. Park, H. Nishiyama, Y. Itoh, K. Itoh, J. Chem. Soc., Chem. Commun., 1994, 1315
48. S. Bachmann, A. Mezzetti, Helv. Chim. Acta, 2001, 84, 3063
49. J. R. Wolf, C. G. Hamaker, J.-P. Djukic, T. Kodadek, L. K. Woo, J. Am. Chem. Soc., 1995, 117, 9194
50. J. M. Fraile, J. I. García, V. Martínez-Merino, J. A. Mayoral, L. Salvatella, J. Am. Chem. Soc., 2001, 123, 7616
51. T. Rasmussen, J. F. Jensen, N. Østergaard, D. Tanner, T. Ziegler, P.-O. Norrby, Chem. Eur, J., 2002, 8, 177
52. H. M. L. Davies, R. E. J. Beckwith, Chem. Rev., 2003, 103, 2861-2903