Bulletin of the Korean Chemical Society

  • 제29권1호
  • /
  • Pages.265-268
  • /
  • 2008
  • /
  • 0253-2964(pISSN)
  • /
  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
권호 표지
DOI QR코드

DOI QR Code

An Expedient Synthesis of β-Phenyl Substituted Baylis-Hillman and Aza-Baylis-Hillman Adducts

  • Kim, Seong-Jin (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Lee, Hyun-Seung (Department of Chemistry and Institute of Basic Science, Chonnam National University) ;
  • Kim, Jeong-Mi (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 : 2008.01.20
PDF 다운로드
⟨ 이전 논문 다음 논문 ⟩

초록

키워드

참고문헌

  1. Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891 https://doi.org/10.1021/cr010043d
  2. Ciganek, E. In Organic Reactions; Paquette, L. A., Ed.; John Wiley & Sons: New York, 1997; Vol. 51, pp 201-350
  3. Basavaiah, D.; Rao, P. D.; Hyma, R. S. Tetrahedron 1996, 52, 8001-8062 https://doi.org/10.1016/0040-4020(96)00154-8
  4. Kim, J. N.; Lee, K. Y. Curr. Org. Chem. 2002, 6, 627-645 https://doi.org/10.2174/1385272023374094
  5. Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 1481-1490 https://doi.org/10.5012/bkcs.2005.26.10.1481
  6. Ramachandran, P. V.; Rudd, M. T.; Burghardt, T. E.; Reddy, M. V. R. J. Org. Chem. 2003, 68, 9310-9316 https://doi.org/10.1021/jo034954u
  7. Ramachandran, P. V.; Reddy, M. V. R.; Rudd, M. T. Chem. Commun. 1999, 1979-1980
  8. Li, G.; Wei, H.-X.; Willis, S. Tetrahedron Lett. 1998, 39, 4607-4610 https://doi.org/10.1016/S0040-4039(98)00850-8
  9. Concellon, J. M.; Huerta, M. J. Org. Chem. 2005, 70, 4714-4719 https://doi.org/10.1021/jo0504969
  10. Li, Q.; Shi, M.; Lyte, J. M.; Li, G. Tetrahedron Lett. 2006, 7699-7702
  11. Shi, Y.-L.; Xu, Y.-M.; Shi, M. Adv. Synth. Catal. 2004, 346, 1220-1230 https://doi.org/10.1002/adsc.200404045
  12. Schmidt, R. R.; Speer, H. Synthesis 1979, 797-798
  13. Thibonnet, J.; Knochel, P. Tetrahedron Lett. 2000, 41, 3319-3322 https://doi.org/10.1016/S0040-4039(00)00387-7
  14. Thibonnet, J.; Vu, V. A.; Berillon, L.; Knochel, P. Tetrahedron 2002, 58, 4787-4799 https://doi.org/10.1016/S0040-4020(02)00439-8
  15. Sato, Y.; Hitomi, K. J. Chem. Soc., Chem. Commun. 1983, 170-171
  16. Semmelhack, M. F.; Stauffer, R. D.; Yamashita, A. J. Org. Chem. 1977, 42, 3180-3188 https://doi.org/10.1021/jo00439a015
  17. Trost, B. M.; Chung, C. K. J. Am. Chem. Soc. 2006, 128, 10358-10359 https://doi.org/10.1021/ja064011p
  18. Park, D. Y.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2007, 48, 1633-1636 https://doi.org/10.1016/j.tetlet.2006.12.146
  19. Park, D. Y.; Gowrisankar, S.; Kim, J. N. Tetrahedron Lett. 2006, 47, 6641-6645 https://doi.org/10.1016/j.tetlet.2006.06.180
  20. Park, D. Y.; Kim, S. J.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2006, 47, 6315-6319 https://doi.org/10.1016/j.tetlet.2006.06.147
  21. Park, D. Y.; Lee, M. J.; Kim, T. H.; Kim, J. N. Tetrahedron Lett. 2005, 46, 8799-8803 https://doi.org/10.1016/j.tetlet.2005.10.034
  22. Lee, M. J.; Kim, S. C.; Kim, J. N. Bull. Korean Chem. Soc. 2006, 27, 439-442 https://doi.org/10.5012/bkcs.2006.27.3.439
  23. Kim, S. C.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 1001-1004 https://doi.org/10.5012/bkcs.2005.26.6.1001
  24. Basavaiah, D.; Pandiaraju, S.; Padmaja, K. Synlett 1996, 393-395
  25. Basavaiah, D.; Krishnamacharyulu, M.; Hyma, R. S.; Pandiaraju, S. Tetrahedron Lett. 1997, 38, 2141-2144 https://doi.org/10.1016/S0040-4039(97)00266-9
  26. Lee, H. J.; Seong, M. R.; Kim, J. N. Tetrahedron Lett. 1998, 39, 6223-6226 https://doi.org/10.1016/S0040-4039(98)01280-5
  27. Kabalka, G. W.; Venkataiah, B.; Dong, G. Org. Lett. 2003, 5, 3803-3805 https://doi.org/10.1021/ol0351798
  28. Shanmugam, P.; Rajasingh, P. Chem. Lett. 2005, 34, 1494-1495 https://doi.org/10.1246/cl.2005.1494
  29. Matsuo, K.; Hasuike, Y. Chem. Pharm. Bull. 1989, 37, 2803-2806 https://doi.org/10.1248/cpb.37.2803
  30. Couche, E.; Fkyerat, A.; Tabacchi, R. Helv. Chim. Acta 2003, 86, 210-221 https://doi.org/10.1002/hlca.200390014
  31. Mal, D.; Dey, S. Tetrahedron 2006, 62, 9589-9602 https://doi.org/10.1016/j.tet.2006.07.090
  32. Du, Y.; Han, X.; Lu, X. Tetrahedron Lett. 2004, 45, 4967-4971 https://doi.org/10.1016/j.tetlet.2004.04.135
  33. Cho, C.-W.; Kong, J.-R.; Krische, M. J. Org. Lett. 2004, 6, 1337-1339 https://doi.org/10.1021/ol049600j
  34. Gong, J. H.; Kim, H. R.; Ryu, E. K.; Kim, J. N. Bull. Korean Chem. Soc. 2002, 23, 789-790 https://doi.org/10.1007/BF02705929
  35. Chen, H.-Y.; Patkar, L. N.; Ueng, S.-H.; Lin, C.-C.; Lee, A. S.-Y. Synlett 2005, 2035-2038
  36. Eagen, M. C.; Cromwell, N. H. J. Org. Chem. 1974, 39, 3863-3866 https://doi.org/10.1021/jo00940a013
  37. Lee, K. Y.; Lee, Y. J.; Kim, J. N. Bull. Korean Chem. Soc. 2007, 28, 143-146 https://doi.org/10.5012/bkcs.2007.28.1.143
  38. Carter, N. B.; Mabon, R.; Richecoeur, A. M. E.; Sweeney, J. B. Tetrahedron 2002, 58, 9117-9129 https://doi.org/10.1016/S0040-4020(02)00995-X
  39. Krauser, S. F.; Watterson, A. C., Jr. J. Org. Chem. 1978, 43, 3400-3402 https://doi.org/10.1021/jo00411a034
  40. Scheiper, B.; Bonnekessel, M.; Krause, H.; Furstner, A. J. Org. Chem. 2004, 69, 3943-3949 https://doi.org/10.1021/jo0498866

피인용 문헌

  1. ChemInform Abstract: An Expedient Synthesis of β-Phenyl-Substituted Baylis-Hillman and Aza-Baylis-Hillman Adducts vol.39, pp.23, 2008, https://doi.org/10.1002/chin.200823030
  2. -Aryl Aza Baylis–Hillman Adducts via Nitroso-Ene Reaction vol.77, pp.16, 2012, https://doi.org/10.1021/jo301266f
  3. Analysis of Bromination of Ethylbenzene Using a 45 MHz NMR Spectrometer: An Undergraduate Organic Chemistry Laboratory Experiment vol.91, pp.8, 2014, https://doi.org/10.1021/ed400365p
  4. A Single-Flask Synthesis of Morita–Baylis–Hillman Adducts from Ethoxyacetylene and Carbonyl Compounds: Synthesis of Subamolides D and E vol.18, pp.16, 2016, https://doi.org/10.1021/acs.orglett.6b01772