Ytterbium triflate catalyzed synthesis of β-functionalized indole derivatives

Tetrahedron Letters

Volumn 52, Issue 5, 2011, Pages 568-571

  Epifano, Francesco ^a   Genovese, Salvatore ^a   Rosati, Ornelio ^b   Tagliapietra, Silvia ^c   Pelucchini, Caroline ^b   Curini, Massimo ^b  

^a UNIVERSITY OF CHIETI   (Italy)

^b UNIVERSITY OF PERUGIA   (Italy)

^c UNIVERSITY OF TURIN   (Italy)

Author keywords

Heterogeneous catalysis; Indole derivatives; Multicomponent reactions; Yonemitsu type reaction; Ytterbium triflate

Indexed keywords

ALDEHYDE; DIMETHYLMALONIC ACID; INDOLE; INDOLE DERIVATIVE; MALONIC ACID DERIVATIVE; SOLVENT; SULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; YTTERBIUM TRIFLATE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; CYCLOADDITION; POLYMERIZATION; RING OPENING; SUBSTITUTION REACTION; SYNTHESIS; YONEMITSU TYPE REACTION;

EID: 78651077508     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.11.128     Document Type: Article

References (18)

1. J. Zhu, and H. Bienaymé Multicomponent Reactions 2005 Wiley-VCH Weinheim pp. 1-21
2. For some recent reviews on multicomponent reactions, see: D.J. Ramon, and M. Yus Angew. Chem., Int. Ed. 44 2005 1602 1634
3. A. Dömling Chem. Rev. 106 2006 17 89
4. Y. Oikawa, H. Hirasawa, and O. Yonemitsu Tetrahedron Lett. 20 1978 1759 1764
5. E. Dardennes, A. Kovács-Kulyassa, A. Renzetti, J. Sapi, and J.Y. Laronze Tetrahedron Lett. 44 2003 221 223
6. F. Cochard, M. Laronze, P. Sigaut, J. Sapi, and J.Y. Laronze Tetrahedron Lett. 45 2004 1703 1708
7. E. Dardennes, A. Kovács-Kulyassa, M. Boisbrun, C. Petermann, J.Y. Laronze, and J. Sapi Tetrahedron: Asymmetry 16 2005 1329 1339
8. L. Jeannin, M. Boisbrun, C. Nemes, F. Cochard, M. Laronze, E. Dardennes, A. Kovács-Kulyassa, J. Sapi, and J.Y. Laronze C. R. Chim. 6 2003 517 528
9. C. Nemes, L. Jeannin, J. Sapi, M. Laronze, H. Seghir, F. Augé, and J.Y. Laronze Tetrahedron 56 2000 5479 5492
10. G. Appendino, L. Cicione, and A. Minassi Tetrahedron Lett. 50 2009 5559 5561
11. A. Renzetti, E. Dardennes, A. Fontana, P. De Maria, J. Sapi, and S. Gerard J. Org. Chem. 73 2008 6824 6827
12. S. Gerard, A. Renzetti, B. Lefvre, A. Fontana, P. De Maria, and J. Sapi Tetrahedron 66 2010 3065 3069
13. S. Kobayashi, M. Sugiura, H. Kitagawa, and W.L. Lam Chem. Rev. 102 2002 2227 2264
14. S. Kobayashi Chem. Lett. 1991 2187 2190
15. S. Genovese, F. Epifano, C. Pelucchini, and M. Curini Eur. J. Org. Chem. 2009 1132 1135 and references cited herein
16. F. Bonadies, A. Lattanzi, L.R. Orelli, S. Pesci, and A. Scettri Tetrahedron Lett. 34 1993 7649 7650
17. M. Fieser Reagents for Organic Synthesis Vol. 14 1989 Wiley-Interscience New York p. 188
18. K.S. Pitzer Acc. Chem. Res. 12 1974 271 276