Expanding the synthetic portfolio of organolithiums: Direct use in catalytic cross-coupling reactions

ChemCatChem

Volumn 6, Issue 6, 2014, Pages 1516-1519

  Pace, Vittorio ^a   Luisi, Renzo ^b  

^a UNIVERSITY OF VIENNA   (Austria)

^b UNIVERSITY OF BARI   (Italy)

Author keywords

C C couplings; organolithium; organometallics; palladium; synthetic methods

Indexed keywords

PALLADIUM;

C-C COUPLING; CARBON-CARBON BOND FORMATION; CROSS COUPLING REACTIONS; ORGANOLITHIUM REAGENT; ORGANOLITHIUMS; PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS; SYNTHETIC METHODS; SYNTHETIC PROCEDURES;

ORGANOMETALLICS;

EID: 84902292937     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201402014     Document Type: Article

References (28)

1. Metal-Catalyzed Cross-Coupling Reactions and More, Vol. 1, 2 and 3 (Eds.:, A. de Meijere, S. Brase, M. Oestreich,), Wiley-VCH, Weinheim, 2014.
2. E.-i. Negishi, Angew. Chem. Int. Ed. 2011, 50, 6738-6764
3. Angew. Chem. 2011, 123, 6870-6897
4. A. Suzuki, Angew. Chem. Int. Ed. 2011, 50, 6722-6737
5. Angew. Chem. 2011, 123, 6854-6869
6. C. C. C. Johansson Seechurn, M. O. Kitching, T. J. Colacot, V. Snieckus, Angew. Chem. Int. Ed. 2012, 51, 5062-5085
7. Angew. Chem. 2012, 124, 5150-5174.
8. J. Clayden, Organolithiums: Selectivity for Synthesis Pergamon, Oxford, 2002
9. The Chemistry of Organolithium Compounds, Vol. 1 and 2 (Eds.:, Z. Rappoport, I. Marek,), Wiley-VCH, Chichester, 2004
10. Lithium Compounds in Organic Synthesis: From Fundamentals to Applications (Eds.:, R. Luisi, V. Capriati,), Wiley-VCH, Weinheim, 2014.
11. S. Murahashi, M. Yamamura, K. Yanagisawa, N. Mita, K. Kondo, J. Org. Chem. 1979, 44, 2408-2417.
12. S.-I. Murahashi, J. Organomet. Chem. 2002, 653, 27-33.
13. T. Luu, Y. Morisaki, N. Cunningham, R. R. Tykwinski, J. Org. Chem. 2007, 72, 9622-9629.
14. K. Fuji, S. Tamba, K. Shono, A. Sugie, A. Mori, J. Am. Chem. Soc. 2013, 135, 12208-12211.
15. A. Nagaki, A. Kenmoku, Y. Moriwaki, A. Hayashi, J.-i. Yoshida, Angew. Chem. Int. Ed. 2010, 49, 7543-7547
16. Angew. Chem. 2010, 122, 7705-7709
17. A. Nagaki, Y. Moriwaki, S. Haraki, A. Kenmoku, N. Takabayashi, A. Hayashi, J.-I. Yoshida, Chem. Asian J. 2012, 7, 1061-1068.
18. A. B. Smith, A. T. Hoye, D. Martinez-Solorio, W.-S. Kim, R. Tong, J. Am. Chem. Soc. 2012, 134, 4533-4536.
19. M. Giannerini, M. Fañanás-Mastral, B. L. Feringa, Nat. Chem. 2013, 5, 667-672.
20. M. Pérez, M. Fañanás-Mastral, P. H. Bos, A. Rudolph, S. R. Harutyunyan, B. L. Feringa, Nat. Chem. 2011, 3, 377-381.
21. M. Giannerini, V. Hornillos, C. Vila, M. Fañanás-Mastral, B. L. Feringa, Angew. Chem. Int. Ed. 2013, 52, 13329-13333
22. Angew. Chem. 2013, 125, 13571-13575.
23. F. R. Leroux, L. Bonnafoux, C. Heiss, F. Colobert, D. A. Lanfranchi, Adv. Synth. Catal. 2007, 349, 2705-2713.
24. V. Hornillos, M. Giannerini, C. Vila, M. Fañanás-Mastral, B. L. Feringa, Org. Lett. 2013, 15, 5114-5117.
25. C. Vila, M. Giannerini, V. Hornillos, M. Fañanás-Mastral, B. L. Feringa, Chem. Sci. 2014, 5, 1361-1367.
26. A. Stoit, W. I. Iwema Bakker, H. Coolen, M. van Dongen, N. J. Leflemme, PCT patent application WO 2012004378 (A1), 2012
27. K. L. Woon, M. P. Aldred, P. Vlachos, G. H. Mehl, T. Stirner, S. M. Kelly, M. O'Neill, Chem. Mater. 2006, 18, 2311-2317
28. L. Liu, C.-L. Ho, W.-Y. Wong, K.-Y. Cheung, M.-K. Fung, W.-T. Lam, A. B. Djurišic̈, W.-K. Chan, Adv. Funct. Mater. 2008, 18, 2824-2833.