Recent development for enantioselective synthesis of aromatic compounds from alkynes via metallacyclopentadienes

Journal of Heterocyclic Chemistry

Volumn 48, Issue 3, 2011, Pages 517-528

  Li, Shi ^a   Zhou, Lishan ^a   Kanno, Ken Ichiro ^a   Takahashi, Tamotsu ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; AROMATIC COMPOUND; CYCLOPENTADIENE DERIVATIVE; HETEROCYCLIC COMPOUND; METAL COMPLEX; METALLACYCLOPENTADIENE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHIRALITY; ENANTIOSELECTIVITY; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 79957460689     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.555     Document Type: Article

References (39)

1. (a), Vollhardt, K. P. C., Acc Chem Res 1977, 10, 1
2. (b), Vollhardt, K. P. C., Angew Chem Int Ed Engl 1984, 23, 539
3. (c), Schore, N. E., Chem Rev 1988, 88, 1081
4. (d), Ojima, I.; Tzamarioudaki, M.; Li, Z.; Donovan, R. J., Chem Rev 1996, 96, 635
5. (e), Kotha, S.; Brahmachary, E.; Lahiri, K. E., J Org Chem 2005, 4741
6. (f), Chopadea, P. R.; Louie, J., Adv Synth Catal 2006, 348, 2307.
7. Sato, Y.; Nishimata, T.; Mori, M., J Org Chem 1994, 59, 6133.
8. (a), Tanaka, K., Synlett 2007, 13, 1977
9. (b), Peña, D.; Pérez, D.; Guitián, E., Chem Record 2007, 7, 326
10. (c), Shibata, T.; Tsuchikama, K., Org Biomol Chem 2008, 6, 1317
11. (d), Ogasawara, M.; Watanabe, S., Synthesis 2009, 11, 1761.
12. (a), Gutnov, A.; Heller, B.; Fischer, C.; Drexler, H.-J.; Spannenberg, A.; Sundermann, B.; Sundermann, C., Angew Chem Int Ed 2004, 43, 3795
13. (b), Tanaka, K.; Nishida, G.; Wada, A.; Noguchi, K., Angew Chem Int Ed 2004, 43, 6510
14. (c), Shibata, T.; Fujimoto, T.; Yokota, K.; Takagi, K., J Am Chem Soc 2004, 126, 8382.
15. Heller, B.; Gutnov, A.; Fischer, C.; Drexler, H.-J.; Spannenberg, A.; Redkin, D.; Sundermann, C.; Sundermann, B., Chem Eur J 2007, 13, 1117.
16. (a), Tanaka, K.; Nishida, G.; Ogino, M.; Hirana, M.; Noguchi, K., Org Lett 2005, 7, 3119
17. (b), Nishida, G.; Noguchi, K.; Hirano, M.; Tanaka, K., Angew Chem Int Ed 2007, 46, 3951
18. (c), Tanaka, K.; Wada, A.; Noguchi, K., Org Lett 2005, 7, 4737
19. (d), Tanaka, K.; Takeichi, K.; Noguchi, K., J Am Chem Soc 2006, 128, 4586
20. (e), Tanaka, K.; Takeichi, K., Synthesis 2007, 18, 2920.
21. Suda, T.; Noguchi, K.; Hirano, M.; Tanaka, K., Chem Eur J 2008, 14, 6593.
22. Shibata, T.; Arai, Y.; Takami, K.; Tsuchikama, K.; Fujimoto, T.; Takebayashi, S.; Takagi, K., Adv Synth Catal 2006, 348, 2475.
23. Nishida, G.; Suzuki, N.; Noguchi, K.; Tanaka, K., Org Lett 2006, 8, 3489.
24. Nishida, G.; Ogaki, S.; Yusa, Y.; Yokozawa, T.; Noguchi, K.; Tanaka, K., Org Lett 2008, 10, 2849.
25. Doherty, S.; Smyth, C. H.; Harrington, R. W.; Clegg, W., Organometallics 2008, 27, 4837.
26. Shibata, T.; Yoshida, S.; Arai, Y.; Otsuka, M.; Endo, K., Tetrahedron 2008, 64, 821.
27. Shibata, T.; Tsuchikama, K.; Otsuka, M., Tetrahedron Asymmetry 2006, 17, 614.
28. Sehnal, P.; Krausová, Z.; Teplý, F.; Stará, I. G.; Starý, I.; Rulíšek, L.; Šaman, D.; Císařová, I., J Org Chem. 2008, 73, 2074.
29. Tanaka, K.; Suda, T.; Noguchi, K.; Hirano, M., J Org Chem 2007, 72, 2243.
30. Oppenheimer, J,;, Hsung, R. P.; Figueroa, R.; Johnson, W. L., Org Lett 2007, 9, 3969.
31. (a), Tanaka, K.; Suzuki, N.; Nishida, G., Eur J Org Chem 2006, 3917
32. (b), Tanaka, K.; Osaka, T.; Noguchi, K.; Hirano, M., Org Lett 2007, 9, 1307
33. (c), Wada, A.; Noguchi, K.; Hirano, M.; Tanaka, K., Org Lett 2007, 9, 1295.
34. Nishida, G.; Noguchi, K.; Hirano, M.; Tanaka, K., Angew Chem Int Ed 2008, 47, 3410.
35. (a), Tanaka, K.; Sagae, H.; Toyoda, K.; Noguchi, K.; Hirano, M., J Am Chem Soc 2007, 129, 1522
36. (b), Tanaka, K.; Sagae, H.; Toyoda, K.; Hirano, M., Tetrahedron 2008, 64, 831.
37. Teplý, F.; Stará, I. G.; Starý, I.; Kollárovič, A.; Šaman, D.; Vyskočil, Š.; Fiedler, P., J Org Chem 2003, 68, 5193.
38. Caeiro, J.; Peña, D.; Cobas, A.; Perez, D.; Guitián, E., Adv Synth Catal 2006, 348, 2466.
39. Tanaka, K.; Kamisawa, A.; Suda, T.; Noguchi, K.; Hirano, M., J Am Chem Soc 2007, 129, 12078.