Reactivity of cationic 1-substituted dicarbonyl (η5-4- methoxycyclohexadienyl)(triphenylphosphine)iron complexes

Tetrahedron Letters

Volumn 39, Issue 16, 1998, Pages 2325-2326

  Millot, Nicolas ^a   Guillou, Catherine ^a   Thal, Claude ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE; CATION; IRON COMPLEX;

ARTICLE; COMPLEX FORMATION; DRUG SYNTHESIS; LIGAND BINDING; MOLECULAR INTERACTION;

EID: 0032537160     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00191-9     Document Type: Article

References (11)

1. 1) Preliminary results concerning this work were presented at the 6th Belgian Organic Synthesis Symposium (BOSS), Gent July 8-12, 1996.
2. 2) Pearson, A.J. Iron Compounds in Organic Synthesis, Best Synthetic Methods ; Academic Press 1994, pp. 97-138.
3. 3) Donaldson, W. A.; Shang, L. Tetrahedron Lett. 1995, 36, 1575-1576.
4. 4) Millot, N.; Guillou, C.; Thal, C. Tetrahedron 1997, 53, 12553-12564.
5. 5) a) Hudson, R.D.A.; Osborne, S.A.; Roberts, E.; Stephenson, G.R. Tetrahedron Lett. 1996, 37, 9009-9012.
6. b) Hudson, R.D.A.; Osborne, S.A.; Stephenson, G.R. Tetrahedron 1997, 53, 4095-4104.
7. 6) Pearson, A.J. ; Chandler, M. J. Chem. Soc. Perkin Trans 1, 1980, 2238-2243.
8. 7) Complexes 6e-g have been previously prepared. Guillou, C.; Millot, N. ; Rboul, V.; Thal, C. Tetrahedron Lett. 1996, 37, 4515-4518.
9. J5-P = 9.2 Hz; C5); 42.8 (C7'); 40.5 (C7'); 39.4 (C6).
10. 9) Howell, J.A.S.; Walton, G.; Tirvengadum, M.C.; Squibb, A.; Palin, M.G. J. Organomet. Chem. 1991, 401, 91-123.
11. 10) Whitesides, T.H; Budnil., R.A. Inorg. Chem. 1975, 174, 664-673.