Pauson-Khand reaction of activated olefins

Tetrahedron Letters

Volumn 40, Issue 30, 1999, Pages 5503-5506

  Ahmar, Mohammed ^a   Antras, Frédéric ^a   Cazes, Bernard ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

Activated olefins; Cobalt complexes; Cycloadditions; Pauson Khand reactions

Indexed keywords

ALKENE DERIVATIVE; ALKYNE DERIVATIVE; CYCLOPENTENONE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; ORGANIC CHEMISTRY;

EID: 0033165960     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01069-2     Document Type: Article

References (17)

1. Khand, I.U.; Knox, G.R.; Pauson, P.L.; Watts, W.E.; Foreman, M.I. J. Chem. Soc. Perkin Trans 1 1973, 977-981.
2. a) Pauson, P.L. Tetrahedron 1985, 41, 5855-5860;
3. b) Shore, N.E. Chem. Rev. 1988, 88, 1081-1119;
4. c) Shore, N.E. In Comprehensive Organic Synthesis, Trost, B.M.; Fleming, I. Eds; Pergamon Press: Oxford 1991, Vol 5 pp. 1037-1064;
5. e) Ingate, S.T.; Marco-Contelles, J. Org. Prep. Proced. Int. 1998, 30, 121-143.
6. Smit, W.A.; Gybin, A.S.; Shashkov, A.S.; Strykov, Y.T.; Michaelian, G.S.; Caple, R.; Swanson, E.D. Tetrahedron Lett. 1986, 27, 1241-1244.
7. Shambayati, S.; Crow, W.E.; Schreiber, S.L. Tetrahedron Lett. 1990, 31, 5289-5292.
8. Chung, Y.K.; Lee, B.Y.; Jeong, N.; Hundecek, M; Pauson, P.L. Organometallics 1993, 12, 220-223.
9. Khand, I.U.; Pauson, P.L. J. Chem. Soc. Chem. Commun. 1974, 379;
10. b) Khand, I.U.; Pauson, P.L. Heterocycles 1978, 11, 59-67.
11. Costa, M.; Mor, A. Tetrahedron Lett. 1995, 36, 2867-2870.
12. In previous work, cyclopentenone 8 was obtained as the major product (15-53% yield) together with the intramolecular Michael addition product generated from 8 and alkyne cyclotrimerization products.
13. +• 55 (51).
14. Mavrov, M.V.; Kucherov, V.F. Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.) 1964,145-146. (Chem. Abstr. 1964, 60, 9160f).
15. Mavrov, M.V.; Kucherov, V.F. Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.) 1964,145-146. (Chem. Abstr. 1964, 60, 9160f).
16. 1H NMR.
17. 7,8