DOI QR코드

DOI QR Code

Synthesis of 2,3,4-Trisubstituted 2,5-Dihydrofuran Derivatives

  • Gowrisankar, Saravanan (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Park, Da-Yeon (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
  • 발행 : 2005.11.20

초록

키워드

참고문헌

  1. Nakamura, M.; Liang, C.; Nakamura, E. Org. Lett. 2004, 6, 2015 https://doi.org/10.1021/ol0493554
  2. Bottex, M.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 175 https://doi.org/10.1021/jo0012997
  3. Marat, X.; Monteiro, N.; Balme, G Synlett 1997, 845
  4. Monteiro, N.; Balme, G. J. Org. Chem. 2000, 65, 3223 https://doi.org/10.1021/jo991817h
  5. Azoulay, S.; Monteiro, N.; Balme, G. Tetrahedron Lett. 2002, 43, 9311 https://doi.org/10.1016/S0040-4039(02)02383-3
  6. Roy, S. C.; Guin, C.; Rana, K. K.; Maiti, G. Tetrahedron 2002, 58, 2435 https://doi.org/10.1016/S0040-4020(02)00113-8
  7. Maiti, G.; Adhikari, S.; Roy, S. C. Tetrahedron 1995, 51, 8389 https://doi.org/10.1016/0040-4020(95)00450-M
  8. Adhikari, S.; Roy, S. C. Tetrahedron Lett. 1992, 33, 6025 https://doi.org/10.1016/S0040-4039(00)61118-8
  9. Roy, S. C.; Adhikari, S. Tetrahedron 1993, 49, 8415 https://doi.org/10.1016/S0040-4020(01)81924-4
  10. Clique, B.; Monteiro, N.; Balme, G. Tetrahedron Lett. 1999, 40, 1301 https://doi.org/10.1016/S0040-4039(98)02631-8
  11. Woods, M.; Monteiro, N.; Balme, G. Eur. J. Org. Chem. 2000, 1711
  12. Hojo, M.; Ishibashi, N.; Hosomi, A. Synlett 1996, 234
  13. Ma, S.; Gao, W. J. Org. Chem. 2002, 67, 6104 https://doi.org/10.1021/jo0163997
  14. Dunach, E.; Esteves, A. P.; Medeiros, M. J.; Olivero, S. Tetrahedron Lett. 2004, 45, 7935 https://doi.org/10.1016/j.tetlet.2004.08.131
  15. Esteves, A. P.; Goken, D. M.; Klein, L. J.; Lemos, M. A.; Medeiros, M. J.; Peters, D. G. J. Org. Chem. 2003, 68, 1024 https://doi.org/10.1021/jo026102k
  16. Maiti, G.; Adhikari, S.; Roy, S. C. J. Chem. Soc., Perkin Trans. 1 1995, 927
  17. Yang, C.; Murray, W. V.; Wilson, L. J. Tetrahedron Lett. 2003, 44, 1783 https://doi.org/10.1016/S0040-4039(03)00083-2
  18. Marco, J. A.; Carda, M.; Rodriguez, S.; Castillo, E.; Kneeteman, M. N. Tetrahedron 2003, 59, 4085 https://doi.org/10.1016/S0040-4020(03)00584-2
  19. Ma, S.; Zhang, J. J. Am. Chem. Soc. 2003, 125, 12386 https://doi.org/10.1021/ja036616g
  20. Garcon, S.; Vassiliou, S.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 4069 https://doi.org/10.1021/jo0017990
  21. Lee, Y. R.; Kim, N. S.; Kim, B. S. Tetrahedron Lett. 1997, 38, 5671 https://doi.org/10.1016/S0040-4039(97)01235-5
  22. Wenkert, E.; Khatuya, H.; Klein, P. S. Tetrahedron Lett. 1999, 40, 5171 https://doi.org/10.1016/S0040-4039(99)01007-2
  23. Ohe, K.; Matsuda, H.; Morimoto, T.; Ogoshi, S.; Chatani, N.; Murai, S. J. Am. Chem. Soc. 1994, 116, 4125 https://doi.org/10.1021/ja00088a077
  24. Gowrisankar, S.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2005, 46, 4859 https://doi.org/10.1016/j.tetlet.2005.05.057
  25. Jana, S.; Guin, C.; Roy, S. C. Tetrahedron Lett. 2005, 46, 1155 https://doi.org/10.1016/j.tetlet.2004.12.079

피인용 문헌

  1. Formal [3+2] cycloaddition of 1-cyanocyclopropane 1-ester with pyridine, quinoline or isoquinoline: a general and efficient strategy for construction of cyanoindolizine skeletons vol.50, pp.65, 2014, https://doi.org/10.1039/C4CC03267E
  2. One-pot synthesis of densely functionalized cyclic $$\beta $$ β -aminoesters containing four stereocenters, based on a $$\hbox {Et}_{3}$$ Et 3 N-promoted pseudo five-component reaction vol.19, pp.1, 2015, https://doi.org/10.1007/s11030-014-9554-2
  3. DBU-mediated [4 + 2] annulations of donor–acceptor cyclopropanes with 3-aryl-2-cyanoacrylates for the synthesis of fully substituted anilines vol.7, pp.61, 2017, https://doi.org/10.1039/C7RA07230A
  4. Synthesis of 2,3,4-Trisubstituted 2,5-Dihydrofuran Derivatives. vol.37, pp.14, 2005, https://doi.org/10.1002/chin.200614117
  5. Dynamic Kinetic Asymmetric Domino Oxa‐Michael/Carbocyclization by Combination of Transition‐Metal and Amine Catalysis: Catalytic Enantioselective Synthesis of Dihydrofurans vol.16, pp.47, 2005, https://doi.org/10.1002/chem.201001992
  6. Efficient and mild synthesis of highly substituted 2,5-dihydrofuran and furan derivatives via stepwise reaction vol.67, pp.19, 2005, https://doi.org/10.1016/j.tet.2011.03.038
  7. DBU‐Mediated [3+2] Cycloaddition Reactions of Donor–Acceptor Cyclopropanes with Nitromethane: Efficient Strategy for the Construction of Isoxazole Skeletons vol.2016, pp.14, 2016, https://doi.org/10.1002/ejoc.201600227
  8. DBU-Promoted Cascade Annulation of Nitroarylcyclopropane-1,1-dicarbonitriles and 3-Aryl-2-cyanoacrylates: An Access to Highly Functionalized Cyclopenta[b]furan Derivatives vol.83, pp.23, 2005, https://doi.org/10.1021/acs.joc.8b02325