Facile synthesis of indenones by cyclopalladated ferrocenylimine-catalyzed annulation of internal alkynes

Applied Organometallic Chemistry

Volumn 25, Issue 9, 2011, Pages 675-679

  Zhang, Junli ^a   Yang, Fan ^a   Wu, Yangjie ^a  

^a ZHENGZHOU UNIVERSITY   (China)

Author keywords

annulation; indenones; internal alkynes; palladium catalysis

Indexed keywords

ANNULATION; BENZOIC ACID; FACILE SYNTHESIS; FERROCENYLIMINE; GOOD YIELD; INDENONES; INTERNAL ALKYNES; PALLADIUM CATALYSIS; REACTION PROCESS; SPEED-UPS;

CARBOXYLIC ACIDS; CATALYSIS; ORGANOMETALLICS; PALLADIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

ACETYLENE;

EID: 80052026718     PISSN: 02682605     EISSN: 10990739     Source Type: Journal    
DOI: 10.1002/aoc.1826     Document Type: Article

References (24)

1. a) E. F. Ullmm, W. A. Henderson Jr, J. Am. Chem. Soc. 1966, 88, 4942
2. b) G. M. Anstead, J. L. Ensign, C. S. Peterson, J. A. Katzenellenbogen, J. Org. Chem. 1989, 54, 1485.
3. G. Zeni, R. C. Larock, Chem. Rev. 2006, 106, 4644 and references therein.
4. W. Tao, L. J. Siverberg, A. L. Rheingold, R. F. Heck, Oganometallics 1989, 8, 2550.
5. J. Vicente, J.-A. Abad, J. Gil-Rubio, J. Organomet. Chem. 1992, 436, C9.
6. R. C. Larock, M. J. Doty, S. Cacchi, J. Org. Chem. 1993, 58, 4579.
7. a) W. A. Herrmann, V. P. M. Böhm, C.-P. Reisinger, J. Organomet. Chem. 1999, 576, 23
8. b) J. Dupont, M. Pfeffer, J. Spencer, Eur. J. Inorg. Chem. 2001, 1917
9. c) R. B. Bedford, C. S. J. Cazin, D. Holder, Coord. Chem. Rev. 2004, 248, 2283
10. d) I. P. Beletskaya, A. V. Cheprakov, J. Organomet. Chem. 2004, 689, 4055
11. e) E. Alacid, D. A. Alonso, L. Botella, C. Nájera, M. C. Pacheco, Chem. Rec. 2006, 6, 117.
12. a) D. A. Alonso, C. Nájera, M. C. Pacheco, Adv. Synth. Catal. 2002, 344, 172
13. b) E. Alacid, C. Nájera, ARKIVOC 2008, viii, 50.
14. a) S.-Q, Huo, Y.-J. Wu, C.-X. Du, Y. Zhu, H.-Z. Yuan, X.-A. Mao, J. Organomet. Chem. 1994, 483, 139
15. b) F. Yang, J.-L. Zhang, Y.-J. Wu, Tetrahedron 2011, 67, 2969
16. c) Y.-J. Wu, F. Yang, J.-L. Zhang, X.-L. Cui, J.-F. Gong, M.-P. Song, T.-S. Li, Chin. Sci. Bull. 2010, 55, 2784
17. d) Y.-T. Leng, F. Yang, K. Wei, Y.-J. Wu, Tetrahedron 2010, 66, 1244
18. e) G.-R. Ren, X.-L. Cui, E.-B. Yang, F. Yang, Y.-J. Wu, Tetrahedron 2010, 66, 4022
19. f) F. Yang, Y.-J. Wu, Eur. J. Org. Chem. 2007, 3476
20. g) F. Yang, X.-L. Cui, Y.-N. Li, J.-L. Zhang, G.-R. Ren, Y.-J. Wu, Tetrahedron 2007, 63, 1963.
21. V. Gevorgyan, L.-G. Quan, Y. Yamamoto, Tetrahedron Lett. 1999, 40, 4089.
22. G. A. Grasa, R. Singh, E. D. Stevens, S. P. Nolan, J. Organomet. Chem. 2003, 687, 269.
23. L. S. Liebeskind, M. S. South, J. Org. Chem. 1980, 45, 5426.
24. M. Antonio, I. Mauro, Tetrahedron Lett. 1965, 34, 3023.