New chiral phosphoramidite allenylidene complexes of ruthenium obtained with chirality transfer

Tetrahedron Letters

Volumn 50, Issue 39, 2009, Pages 5485-5488

  Costin, Stephen ^a   Rath, Nigam P ^a,b   Bauer, Eike B ^a  

^a UNIVERSITY OF MISSOURI ST LOUIS   (United States)

^b UNIVERSITY OF MISSOURI ST LOUIS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLENE DERIVATIVE; METAL COMPLEX; PHOSPHORAMIDOUS ACID; RUTHENIUM COMPLEX;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; COMPLEX FORMATION; DIASTEREOISOMER; LIGAND BINDING; PRECURSOR; REACTION ANALYSIS; SYNTHESIS; X RAY ANALYSIS;

EID: 68349137693     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.07.069     Document Type: Article

References (32)

1. Reviews and recent examples:. Winter R.F., and Záliš S. Coord. Chem. Rev. 248 (2004) 1565
2. Bruce M.I. Chem. Rev. 98 (1998) 2797
3. Werner H. Chem. Commun. (1997) 903
4. Cadierno V., Gamasa M.P., Gimeno J., González-Cueva M., Lastra E., Borge J., García-Granda S., and Pérez-Carrenõ E. Organometallics 15 (1996) 2137
5. Pino-Chamorro J.A., Bustelo E., Puerta M.C., and Valerga P. Organometallics 28 (2009) 1546
6. Kessler F., Szesni N., Põhako K., Weibert B., and Fischer H. Organometallics 28 (2009) 348
7. Castarlenas R., Esteruelas M.A., Lalrempuia R., Oliván M., and Oñate E. Organometallics 27 (2008) 795
8. Fischer E.O., Kalder H.J., Frank A., Kohler H., and Huttner G. Angew. Chem., Int. Ed. Engl. 15 (1976) 623
9. Berke H. Angew. Chem., Int. Ed. Engl. 15 (1976) 624
10. Selegue J.P. Organometallics 1 (1982) 217
11. Castarlenas R., Vovard C., Fischmeister C., and Dixneuf P.H. J. Am. Chem. Soc. 128 (2006) 4079
12. Bruneau C., and Dixneuf P.H. Angew. Chem., Int. Ed 45 (2006) 2176
13. Nishibayashi Y., and Uemura S. Curr. Org. Chem. 10 (2006) 135
14. Cadierno V., Gamasa M.P., and Gimeno J. Eur. J. Inorg. Chem. (2001) 571
15. Representative example:. Yada Y., Miyake Y., and Nishibayashi Y. Organometallics 27 (2008) 3614
16. Representative examples:. Nishibayashi Y., Milton M.D., Inada Y., Yoshikawa M., Wakiji I., Hidai M., and Uemura S. Chem. Eur. J. 11 (2005) 1433
17. Cadierno V., Diez J., Garcia-Garrido S.E., and Gimeno J. Chem. Commun. (2004) 2716
18. Fukamizu K., Miyake Y., and Nishibayashi Y. J. Am. Chem. Soc. 130 (2008) 10498
19. Cadierno V., Conejero S., Gamasa M.P., and Gimeno J. Dalton Trans. (2003) 3060
20. Cadierno V., Conejero S., Gamasa M.P., Gimeno J., Falvello L.R., and Llusar R.M. Organometallics 21 (2002) 3716
21. García-Fernández A., Gimeno J., Lastra E., Madrigal C.A., Graiff C., and Tiripicchio A. Eur. J. Inorg. Chem. (2007) 732
22. Zhong Y.-W., Matsuo Y., and Nakamura E. Chem. Asian J. 2 (2007) 358
23. Costin S., Rath N.P., and Bauer E.B. Inorg. Chim. Acta 362 (2009) 1935
24. Costin S., Rath N.P., and Bauer E.B. Adv. Synth. Catal. 350 (2008) 2414
25. Hulst R., de Vries N.K., and Feringa B.L. Tetrahedron: Asymmetry 5 (1994) 699
26. Feringa B.L. Acc. Chem. Res. 33 (2000) 346
27. Representative example:. Minnaard A.J., Feringa B.L., Lefort L., and de Vries J.G. Acc. Chem. Res. 40 (2007) 1267
28. 31P), HRMS, IR and most of them by elemental analyses, and full experimental details and characterization data are given in the Supplementary data.
29. Oro L.A., Ciriano M.A., and Campo M. J. Organomet. Chem. 289 (1985) 117
30. 2 = 0.1271/0.1063/0.0862 (all data).
31. Cadierno V., Conejero S., Gamasa M.P., Gimeno J., and Rodríguez M.A. Organometallics 21 (2002) 203
32. Cadierno V., Gamasa M.P., Gimeno J., Borge J., and García-Granda S. Organometallics 16 (1997) 3178