Chiral Tricarbonyl(η6Arene)Chromium(0) Complexes in Stereoselective Hetero Diels-Alder Reactions

Synlett

Volumn 1996, Issue 3, 1996, Pages 258-260

  Baldoli, Clara ^a   Del Buttero, Paola ^a   Di Ciolo, Michela ^a   Maiorana, Stefano ^a   Papagni, Antonio ^a  

^a CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 1542740617     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1996-5382     Document Type: Article

References (18)

1. Carruthers, W. in Cycloaddition Reaction in Organic Synthesis; Tetrahedron Organic Chemistry Series Vol. 8; Pergamon Press: Oxford, UK 1990. De Simoni, G.; Tacconi, G. Chem Rev. 1975, 75, 651.
2. Carruthers, W. in Cycloaddition Reaction in Organic Synthesis; Tetrahedron Organic Chemistry Series Vol. 8; Pergamon Press: Oxford, UK 1990. De Simoni, G.; Tacconi, G. Chem Rev. 1975, 75, 651.
3. Danishefsky, S.J.; De Ninno, M.P.; Angew. Chem. Int. Ed. Engl. 1987, 26, 15. Danishefsky, S. J. Chemtracts 1989, 273.
4. Danishefsky, S.J.; De Ninno, M.P.; Angew. Chem. Int. Ed. Engl. 1987, 26, 15. Danishefsky, S. J. Chemtracts 1989, 273.
5. Waldmann, H. Synthesis 1994, 535.
6. Uemura, M.; Hayashi, Y; Hayashy, Y.; Tetrahedron: Asymmetry 1993, 4, 2291.
7. a) Baldoli, C.; Del Buttero, P.; Maiorana, S.; Moret, M.; Zecchi, G. Tetrahedron Lett. 1993, 34, 2529.
8. b) Baldoli, C.; Del Buttero, P.; Licandro, E.; Maiorana, S.; Papagni, A.; Albinati, A. Tetrahedron: Asymmetry 1995, 6, 1711.
9. A preliminary account of this work was presented as poster communication at "XVIth International Conference on Organometallic Chemistry" University of Sussex, Brighton 10-15 July 1994.
10. Baldoli, C.; Del Buttero, P. J. Chem. Soc. Chem. Commun. 1991, 982.
11. All new compounds gave satisfactory spectroscopic and analytical data.
12. 3); 5.04 (d, 1H, J=6.2 Hz, arom.); 5.10 (t, 1H, J=6.4 Hz, arom.); 5.20 (d, 1H, J=7.90 Hz, CH); 5.29 (d, 1H, J=7.84 Hz, CH=); 5.35 (t, 1H, J=6.2 Hz, arom.); 5.58 (d, 1H, J=6.4 Hz, arom.); 6.9-7.3 (m, 4H, arom.); 7.54 (d, 1H, J=7.84 Hz, CH=).
13. 3); 5.21 (d, 1H, J=7.71 Hz, CH=); 5.32 (dd, 1H, J=4.7 Hz, J=7.76 Hz, CH); 6.7-7.4 (m, 8H, arom.); 7.58 (d, 1H, J=7.71 Hz, CH=).
14. Baldoli, C.; Del Buttero, P.; Licandro, E.; Maiorana, S.; Papagni, A. Synlett 1994, 183.
15. 3); 4.92 (t, 1H, J=6.3 Hz, arom.); 5.05 (d, 1H, J=6.8 Hz, arom.); 5.45 (dd, 1H, J=14.2 Hz, J=4.1 Hz, CH); 5.51-5.57 (m, 2H, arom+CH=); 5.8 (d, 1H, J=6.30 Hz, arom.); 7.53 (d, 1H, J= 6.1 Hz, CH=).
16. 3).
17. Danishefsky, S. J.; Kerwin, F. K. Jr.; Kobayashi, S. J. Am. Chem. Soc. 1982, 104, 358. Danishefsky, S. J.; Larson, E. R. J. Am. Chem. Soc. 1982, 104, 6458.
18. Danishefsky, S. J.; Kerwin, F. K. Jr.; Kobayashi, S. J. Am. Chem. Soc. 1982, 104, 358. Danishefsky, S. J.; Larson, E. R. J. Am. Chem. Soc. 1982, 104, 6458.