The first example of an enantiopure planar chiral hydroxyferrocene ligand

Tetrahedron Asymmetry

Volumn 10, Issue 21, 1999, Pages 4095-4097

  Pickett, Tom E ^a   Richards, Christopher J ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

FERROCENE DERIVATIVE; LIGAND;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOMER; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0033455625     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00450-4     Document Type: Article

References (19)

1. For recent reviews, see: (a) Richards, C. J.; Locke, A. J. Tetrahedron: Asymmetry 1998, 9, 2377. (b) Kagan, H. B.; Riant, O. Advances in Asymmetric Synthesis; Hassner, A., Ed.; JAI Press Inc.: Greenwich, CT, 1997; Vol. 2, pp. 189-235.
2. For recent reviews, see: (a) Richards, C. J.; Locke, A. J. Tetrahedron: Asymmetry 1998, 9, 2377. (b) Kagan, H. B.; Riant, O. Advances in Asymmetric Synthesis; Hassner, A., Ed.; JAI Press Inc.: Greenwich, CT, 1997; Vol. 2, pp. 189-235.
3. Schnyder, A.; Hintermann, L.; Togni, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 931.
4. Togni, A.; Breutel, C.; Schnyder, A.; Spindler, F.; Landert, H.; Tijani, A. J. Am. Chem. Soc. 1994, 116, 4062.
5. Nishibayashi, Y.; Singh, J. D.; Fukuzawa, S.; Uemura, S. J. Chem. Soc., Perkin Trans. 1 1995, 2871.
6. Nesmeyanov, A. N.; Sazonova, V. A.; Drozd, V. N. Tetrahedron Lett. 1959, 17, 13.
7. Nesmeyanov, A. N.; Sazonova, V. A.; Drozd, V. N. Chem. Ber. 1960, 93, 2717.
8. Epton, R.; Marr, G.; Rogers, G. K. J. Organomet. Chem. 1978, 150, 93.
9. Onishi, M.; Hiraki, K.; Iwamoto, A. J. Organomet. Chem. 1984, 262, C11.
10. (a) Richards, C. J.; Damalidis, T.; Hibbs, D. E.; Hursthouse, M. B. Synlett 1995, 74.
11. (b) Sammakia, T.; Latham, H. A.; Schaad, D. R. J. Org. Chem. 1995, 60, 10.
12. (c) Nishibayashi, Y.; Uemura, S. Synlett 1995, 79.
13. (d) Sammakia, T.; Latham, H. A. J. Org. Chem. 1995, 60, 6002.
14. Jackson, W. P. Synlett 1990, 536.
15. Herberhold, M.; Brendel, H.-D.; Hofmann, A.; Hofmann, B.; Milius, W. J. Organomet. Chem. 1998, 556, 173.
16. 2O and hexane) and drying gave 10 as a brown powder (1.0 g, 45%).
17. +, 14%), 283 (52), 268 (38), 211 (31), 121 (100).
18. +, 16%), 313 (72), 227 (71), 121 (100).
19. 2 requires: 313.0765).