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Synthesis 2012; 44(20): 3109-3128
DOI: 10.1055/s-0032-1316778
DOI: 10.1055/s-0032-1316778
review
1,6-Conjugate Addition of Nucleophiles to α,β,γ,δ-Diunsaturated Systems
Weitere Informationen
Publikationsverlauf
Received: 01. Juli 2012
Accepted after revision: 07. August 2012
Publikationsdatum:
12. September 2012 (online)
Abstract
Herein, an overview of the most important developments and concepts related to the 1,6-conjugate addition reactions are reviewed.
1 Introduction
2 Transition-Metal-Catalyzed 1,6-Conjugate Additions
2.1 Copper-Mediated Reactions
2.2 Iron-Mediated Reactions
2.3 Rhodium- and Iridium-Mediated Reactions
3 Organocatalyzed 1,6-Conjugate Additions
4 Other Methods
5 Conclusions
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References
- 1 Perlmutter P. Conjugate Addition Reactions in Organic Synthesis. Pergamon Press; Oxford: 1992
- 2a Vuagnoux-d’Augustin M, Alexakis A. Chem.–Eur. J. 2007; 13: 9647
- 2b Alexakis A, Benhaim C. Eur. J. Org. Chem. 2002; 3221
- 2c Krause N, Hoffmann-Röder A. Synthesis 2001; 171
- 2d Hayashi T. Acc. Chem. Res. 2000; 33: 354
- 3 Almasi D, Alonso DA, Najera C. Tetrahedron: Asymmetry 2007; 18: 299
- 4a Csákÿ AG, Herrán G, Murcia MC. Chem. Soc. Rev. 2010; 39: 4080
- 4b Frederik MA, Hulce M. Tetrahedron 1997; 53: 10197
- 4c Ralls JW. Chem. Rev. 1959; 59: 329
- 5 Krause N, Thorand S. Inorg. Chim. Acta 1999; 296: 1
- 6 Näf F, Degen P, Ohloff G. Helv. Chim. Acta 1972; 55: 82
- 7 Corey EJ, Kim CU, Chen RH. K, Takeda M. J. Am. Chem. Soc. 1972; 94: 4395
- 8 Yamamoto Y, Yamamoto S, Yatagai H, Ishihara Y, Maruyama K. J. Org. Chem. 1982; 47: 119
- 9a Hulce M. Tetrahedron Lett. 1988; 29: 5851
- 9b Cheng M, Hulce M. J. Org. Chem. 1990; 55: 964
- 9c Krause N. Chem. Ber. 1990; 123: 2173
- 9d Krause N, Gerold A. Angew. Chem., Int. Ed. Engl. 1997; 36: 186 ; and references therein
- 9e Canisius J, Gerold A, Krause N. Angew. Chem. Int. Ed. 1999; 38: 1644 ; and references therein
- 10 Uerdingen M, Krause N. Tetrahedron 2000; 56: 2799
- 11 Yoshikai N, Yamashita T, Nakamura E. Chem.–Asian J. 2006; 1: 322
- 12 Fillion E, Wilsily A, Liao E.-T. Tetrahedron: Asymmetry 2006; 17: 2957
- 13 Hartog T, Harutyunyan SR, Font D, Minnaard AJ, Feringa BL. Angew. Chem. Int. Ed. 2008; 47: 398
- 14 Hartog T, Dijken DJ, Minnaard AJ, Feringa BL. Tetrahedron: Asymmetry 2010; 21: 1574
- 15a Hénon H, Mauduit M, Alexakis A. Angew. Chem. Int. Ed. 2008; 47: 9122
- 15b Tissot M, Poggiali D, Hénon H, Müller D, Guénée L, Mauduit M, Alexakis A. Chem.–Eur. J. 2012; 18: 8731
- 16 Lee K, Hoveyda AH. J. Am. Chem. Soc. 2010; 132: 2898
- 17 Tissot M, Müller D, Belot S, Alexakis A. Org. Lett. 2010; 12: 2770
- 18 Wencel-Delord J, Alexakis A, Crévisy C, Mauduit M. Org. Lett. 2010; 12: 4335
- 19 Fukuhara K, Urabe H. Tetrahedron Lett. 2005; 46: 603
- 20 Okada S, Arayama K, Murayama R, Ishizuka T, Hara K, Hirone N, Hata T, Urabe H. Angew. Chem. Int. Ed. 2008; 47: 6860
- 21 Hayashi T, Tokunaga N, Inoue K. Org. Lett. 2004; 6: 305
- 22 Hayashi T, Yamamoto S, Tokunaga N. Angew. Chem. Int. Ed. 2005; 44: 4224
- 23 Herrán G, Murcia C, Csákÿ AG. Org. Lett. 2005; 7: 5629
- 24 Herrán G, Csákÿ AG. Synlett 2009; 585
- 25a Tseng N.-W, Mancuso J, Lautens M. J. Am. Chem. Soc. 2006; 128: 5338
- 25b Tseng N.-W, Lautens M. J. Org. Chem. 2009; 74: 2521
- 26 Baba H, Chen J, Shinokubo H, Osuka A. Chem.–Eur. J. 2008; 14: 4256
- 27 Nishimura T, Makino H, Nagaosa M, Hayashi T. J. Am. Chem. Soc. 2010; 132: 12865
- 28 Roscales S, Salado IG, Csákÿ AG. Synlett 2011; 2234
- 29 Nishimura T, Yasuhara Y, Hayashi T. Angew. Chem. Int. Ed. 2006; 45: 5164
- 30 Nishimura T, Yasuhara Y, Sawano T, Hayashi T. J. Am. Chem. Soc. 2010; 132: 7872
- 31 Nishimura T, Noishiki A, Hayashi T. Chem. Commun. 2012; 48: 973
- 32 Bernardi L, López-Cantarero J, Niess B, Jørgensen KA. J. Am. Chem. Soc. 2007; 129: 5772
- 33 Murphy JJ, Quintard A, McArdle P, Alexakis A, Stephens JC. Angew. Chem. Int. Ed. 2011; 50: 5095
- 34 Sun H.-W, Liao Y.-H, Wu Z.-J, Wang H.-Y, Zhang X.-M, Yuan W.-C. Tetrahedron 2011; 67: 3991
- 35 Tian X, Liu Y, Melchiorre P. Angew. Chem. Int. Ed. 2012; 51: 6439
- 36 Gong H, Andrews RS, Zuccarello JL, Lee SJ, Gagné MR. Org. Lett. 2009; 11: 879
- 37 Silva EM. P, Silva AM. S, Cavaleiro JA. S. Synlett 2011; 2740
- 38 Ballini R, Bosica G, Fiorini D. Tetrahedron Lett. 2001; 42: 8471
- 39 Caro B, Le Poul P, Robin-Le Guen F, Sénéchal-Tocquer M.-C, Saillard J.-Y, Kahlal S, Ouahab L, Golhen S. Eur. J. Org. Chem. 2000; 577
- 40 Kusama H, Sawada T, Okita A, Shiozawa F, Iwasawa N. Org. Lett. 2006; 8: 1077
- 41 Brooks JL, Caruana PA, Frontier AJ. J. Am. Chem. Soc. 2011; 133: 12454
- 42 Brocchini SJ, Lawton RG. Tetrahedron Lett. 1997; 38: 6319