Advances in Asymmetric Borrowing Hydrogen Catalysis

ChemSusChem

Volumn , Issue , 2014, Pages 2411-2413

  Hollmann, Dirk ^a  

^a LEIBNIZ INSTITUT FÜR KATALYSE E V AN DER UNIVERSITÄT ROSTOCK   (Germany)

Author keywords

asymmetric catalysis; borrowing hydrogen; enantioselectivity; organocatalysis; synthetic methods

Indexed keywords

EID: 84927917015     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.201402320     Document Type: Article

References (30)

1. R. A. Sheldon, Chem. Commun. 2008, 3352–3365.
2. S. Bähn, S. Imm, L. Neubert, M. Zhang, H. Neumann, M. Beller, ChemCatChem 2011, 3, 1853–1864;
3. A. J. A. Watson, J. M. J. Williams, Science 2010, 329, 635–636;
4. G. Guillena, D. J. Ramón, M. Yus, Chem. Rev. 2010, 110, 1611–1641.
5. J. Schranck, A. Tlili, M. Beller, Angew. Chem. Int. Ed. 2013, 52, 7642–7644;
6. Angew. Chem. 2013, 125, 7795–7797.
7. Y. Zhao, S. W. Foo, S. Saito, Angew. Chem. Int. Ed. 2011, 50, 3006–3009;
8. Angew. Chem. 2011, 123, 3062–3065.
9. D. J. Shermer, P. A. Slatford, D. D. Edney, J. M. J. Williams, Tetrahedron: Asymmetry 2007, 18, 2845–2848.
10. Moderate enantiomeric excess (<70 %) was reported by Oe and co-workers: A. Eka Putra, Y. Oe, T. Ohta, Eur. J. Org. Chem. 2013, 6146–6151.
11. A. Quintard, T. Constantieux, J. Rodriguez, Angew. Chem. Int. Ed. 2013, 52, 12883–12887;
12. Angew. Chem. 2013, 125, 13121–13125.
13. Y. Zhang, C.-S. Lim, D. S. B. Sim, H.-J. Pan, Y. Zhao, Angew. Chem. Int. Ed. 2014, 53, 1399–1403;
14. Angew. Chem. 2014, 126, 1423–1427.
15. S. Bertelsen, K. A. Jørgensen, Chem. Soc. Rev. 2009, 38, 2178–2189.
16. A. Pagnoux-Ozherelyeva, N. Pannetier, M. D. Mbaye, S. Gaillard, J.-L. Renaud, Angew. Chem. Int. Ed. 2012, 51, 4976–4980;
17. Angew. Chem. 2012, 124, 5060–5064 and references therein.
18. R. J. Phipps, G. L. Hamilton, F. D. Toste, Nat. Chem. 2012, 4, 603–614.
19. W. Tang, S. Johnston, J. A. Iggo, N. G. Berry, M. Phelan, L. Lian, J. Bacsa, J. Xiao, Angew. Chem. Int. Ed. 2013, 52, 1668–1672;
20. Angew. Chem. 2013, 125, 1712–1716.
21. M. Rueping, R. M. Koenigs, I. Atodiresei, Chem. Eur. J. 2010, 16, 9350–9365.
22. C. Gunanathan, D. Milstein, Angew. Chem. Int. Ed. 2008, 47, 8661–8664;
23. Angew. Chem. 2008, 120, 8789–8792;
24. D. Pingen, C. Müller, D. Vogt, Angew. Chem. Int. Ed. 2010, 49, 8130–8133;
25. Angew. Chem. 2010, 122, 8307–8310.
26. O. Saidi, A. J. Blacker, M. M. Farah, S. P. Marsden, J. M. J. Williams, Angew. Chem. Int. Ed. 2009, 48, 7375–7378;
27. Angew. Chem. 2009, 121, 7511–7514;
28. D. Hollmann, S. Baehn, A. Tillack, M. Beller, Angew. Chem. Int. Ed. 2007, 46, 8291–8294;
29. Angew. Chem. 2007, 119, 8440–8444.
30. S. Mukherjee, J. W. Yang, S. Hoffmann, B. List, Chem. Rev. 2007, 107, 5471–5569.