A general access to 1,1-cyclopropane aminoketones and their conversion into 2-benzoyl quinolines

Chemical Communications

Volumn 48, Issue 79, 2012, Pages 9927-9929

  Mao, Zhenjun ^a   Qu, Haijun ^a   Zhao, Yanyan ^a   Lin, Xufeng ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1,1 CYCLOPROPANE AMINOKETONE DERIVATIVE; 2 BENZOYLQUINOLINE DERIVATIVE; AMINOKETONE; CYCLOPROPANE DERIVATIVE; QUINOLINE DERIVATIVE; SULFONIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; METHODOLOGY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION OPTIMIZATION; STRUCTURE ANALYSIS; X RAY ANALYSIS;

EID: 84866252612     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c2cc35235d     Document Type: Article

References (28)

1. H.-W. Liu and C. T. Walsh, The Chemistry of the Cyclopropyl Group, ed. Z. Rappoport, John Wiley & Sons Ltd., New York, 1987
2. L. A. Wessjohann, W. Brandt, Chem. Rev., 2003, 103, 1625.
3. H. U. Reissig, R. Zimmer, Chem. Rev., 2003, 103, 1151.
4. F. Gnad, O. Reiser, Chem. Rev., 2003, 103, 1603.
5. H. Lebel, J. F. Marcoux, C. Molinaro, A. B. Charette, Chem. Rev., 2003, 103, 977.
6. W. A. Donaldson, Tetrahedron, 2001, 57, 8589.
7. J. Nurbo, S. D. Peterson, G. Dahl, U. H. Danielson, A. Karlena, A. Sandstrom, Bioorg. Med. Chem., 2008, 16, 5590.
8. K. Mitsuru, S. Hirosada, M. Iwao, K. Kiyohisa, K. Seiji, N. Shunsaku, S. Yasushi, Chem. Pharm. Bull., 1981, 29, 1912.
9. J. Gosselck, L. Béress, H. Schenk, Angew. Chem., Int. Ed. Engl., 1966, 5, 596.
10. M. G. Unthank, N. Hussain, V. K. Aggarwal, Angew. Chem., Int. Ed., 2006, 45, 7066.
11. M. G. Unthank, B. Tavassoli, V. K. Aggarwal, Org. Lett., 2008, 10, 1501.
12. M. Yar, E. McGarrigle, V. K. Aggarwal, Org. Lett., 2009, 11, 257.
13. M. Yar, E. McGarrigle, V. K. Aggarwal, Angew. Chem., Int. Ed., 2008, 47, 3784.
14. C. S. Xie, D. Y. Han, J. H. Liu, T. Xie, Tetrahedron Lett., 2010, 51, 5238.
15. H. Yamanaka, T. Muaiyama, Chem. Lett., 2003, 32, 1192.
16. H. Yamanaka, J. I. Matsuo, A. Kawana, T. Muaiyama, Chem. Lett., 2003, 32, 626.
17. J. I. Matsuo, H. Yamanaka, A. Kawana, T. Muaiyama, Chem. Lett., 2003, 32, 392.
18. H. Yamanaka, J. I. Matsuo, A. Kawana, T. Muaiyama, ARKIVOC, 2004, 42.
19. S. P. Fritz, J. F. Moya, M. G. Unthank, E. M. McGarrigle, V. K. Aggarwal, Synthesis, 2012, 1584.
20. J. Gosselck, H. Ahlbrecht, F. Dost, H. Schenk, G. Schmidt, Tetrahedron Lett., 1968, 9, 995.
21. J. Gosselck, G. Schmidt, Angew. Chem., Int. Ed. Engl., 1968, 7, 456.
22. J. Gosselck, G. Schmidt, L. Beress, H. Schenk, Tetrahedron Lett., 1968, 9, 331.
23. J. Gosselck, G. Schmidt, Tetrahedron Lett., 1969, 10, 2615.
24. X. F. Lin, Z. J. Mao, X. Dai, P. Lu, Y. G. Wang, Chem. Commun., 2011, 47, 6620.
25. D. J. Blythin, S. Kuo, H. Shue, A. Mcphail, R. Chapman, W. Kreutner, C. Rizzo, H. She, R. West, Bioorg. Med. Chem. Lett., 1996, 6, 1529.
26. J. P. Michael, Nat. Prod. Rep., 1997, 14, 605.
27. M. Movassaghi, M. D. Hill, J. Am. Chem. Soc., 2006, 128, 4592.
28. O. Tsuge, H. Watanabe, Heterocycles, 1976, 4, 1905.