Chiral Brønsted acid-catalyzed enantioselective addition of indoles to ketimines

Organic and Biomolecular Chemistry

Volumn 12, Issue 5, 2014, Pages 724-727

  Kano, Taichi ^a   Takechi, Ryosuke ^a   Kobayashi, Ryohei ^a   Maruoka, Keiji ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ENANTIOSELECTIVITY;

ENANTIOSELECTIVE ADDITION; KETIMINES; ORGANOCATALYTIC;

CATALYSIS;

EID: 84891869771     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob42190b     Document Type: Article

References (42)

1. P. I. Dalko L. Moisan Angew. Chem., Int. Ed. 2001 40 3726
2. P. I. Dalko L. Moisan Angew. Chem., Int. Ed. 2004 43 5138
3. A. Berkessel and H. Gröger, Asymmetric Organocatalysis: From Biomimetic Concepts to Applications in Asymmetric Synthesis, Wiley-VCH, Weinheim, 2005
4. Enantioselective Organocatalysis, ed., P. I. Dalko, Wiley-VCH, Weinheim, 2007
5. M. Terada Synthesis 2010 1929
6. W. Zhuang S. Saaby K. A. Jørgensen Angew. Chem., Int. Ed. 2004 43 4476
7. V. A. Sukach N. M. Golovach V. V. Pirozhenko E. B. Rusanov M. V. Vovk Tetrahedron: Asymmetry 2008 19 761
8. Z. Hou J. Wang X. Liu X. Feng Chem.-Eur. J. 2008 14 4484
9. B. Jiang J. J. Dong Y. G. Si X. L. Zhao Z. G. Huang M. Xua Adv. Synth. Catal. 2008 350 1360
10. C. Baudequin A. Zamfir S. B. Tsogoeva Chem. Commun. 2008 4637
11. D. Enders K. Gottfried G. Raabe Adv. Synth. Catal. 2010 352 3147
12. N. Hara R. Tamura Y. Funahashi S. Nakamura Org. Lett. 2011 13 16621
13. L. Li M. Han M. Xiao Z. Xie Synlett 2011 1727
14. Y.-L. Liu T.-D. Shi F. Zhou X.-L. Zhao X. Wang J. Zhou Org. Lett. 2011 13 3826
15. T. Kano S. Song Y. Kubota K. Maruoka Angew. Chem., Int. Ed. 2012 51 1191
16. N. Hara S. Nakamura M. Sano R. Tamura Y. Funahashi N. Shibata Chem.-Eur. J. 2012 18 9276
17. W. Yan D. Wang J. Feng P. Li D. Zhao R. Wang Org. Lett. 2012 14 2512
18. A. Parra R. Alfaro L. Marzo A. Moreno-Carrasco J. L. G. Ruano J. Alemán Chem. Commun. 2012 48 9759
19. F.-G. Zhang X.-Y. Zhu S. Li J. Niea J.-A. Ma Chem. Commun. 2012 48 11552
20. D. Wang J. Liang J. Feng K. Wang Q. Sun L. Zhao D. Li W. Yan R. Wang Adv. Synth. Catal. 2013 355 548
21. Y.-X. Jia J. Zhong S.-F. Zhu C.-M. Zhang Q.-L. Zhou Angew. Chem., Int. Ed. 2007 46 5565
22. M. Abid L. Teixeira B. Török Org. Lett. 2008 10 933
23. M. Rueping B. J. Nachtsheim Synlett 2010 119
24. M. Rueping S. Raja A. Núñez Adv. Synth. Catal. 2011 353 563
25. R. Husmann E. Sugiono S. Mersmann G. Raabe M. Rueping C. Bolm Org. Lett. 2011 13 1044
26. X. Yu Y. Wang G. Wu H. Song Z. Zhou C. Tang Eur. J. Org. Chem. 2011 3060
27. J. Hermeke P. H. Toy Tetrahedron 2011 67 4103
28. Q. Yin S.-L. You Chem. Sci. 2011 2 1344
29. M. Righi F. Bartoccini S. Lucarini G. Piersanti Tetrahedron 2011 67 7923
30. E. Aranzamendi N. Sotomayor E. Lete J. Org. Chem. 2012 77 2986
31. J. Feng W. Yan D. Wang P. Li Q. Sun R. Wang Chem. Commun. 2012 48 8003
32. Y. Qian C. Jing C. Zhai W.-h. Hu Adv. Synth. Catal. 2012 354 301
33. R. Bloch Chem. Rev. 1998 98 1407
34. D. A. Cogan J. A. Ellman J. Am. Chem. Soc. 1999 121 268
35. O. Riant J. Hannedouche Org. Biomol. Chem. 2007 5 873
36. M. Shibasaki M. Kanai Chem. Rev. 2008 108 2853
37. J. Clayden M. Donnard J. Lefranc D. Tetlow Chem. Commun. 2011 47 4624
38. M. Terada K. Sorimachi J. Am. Chem. Soc. 2007 129 292
39. Q. Kang Z.-A. Zhao S.-L. You J. Am. Chem. Soc. 2007 129 1484
40. H. Miyabe Y. Yamaoka Y. Takemoto J. Org. Chem. 2006 71 2099
41. S. Kobayashi J. Kobayashi H. Ishiani M. Ueno Chem.-Eur. J. 2002 8 4185
42. J. Wolfer T. Bekele C. J. Abraham C. Dogo-Isonagie T. Lectka Angew. Chem., Int. Ed. 2006 45 7398