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Volumn 43, Issue 44, 2002, Pages 7983-7985

Facile synthesis of enantiopure tricyclic furanyl derivatives via tungsten-mediated cycloalkenation reactions and Diels-Alder reactions

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXANE DERIVATIVE; ACETALDEHYDE; ALCOHOL DERIVATIVE; ALKADIENE; ALKENE; CYCLOALKENE; FUNCTIONAL GROUP; FURAN DERIVATIVE; HYDROGEN; NITROGEN DERIVATIVE; TUNGSTEN;

EID: 0037190866     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01815-4     Document Type: Article
Times cited : (7)

References (25)
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    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1999) Phytochemistry , vol.52 , pp. 1633
    • Flegel, M.1    Adam, K.-L.2    Becker, H.3
  • 2
    • 0001555531 scopus 로고
    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 4342
    • Finnegan, R.A.1    Djerassi, C.2
  • 3
    • 0343487881 scopus 로고    scopus 로고
    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6737
    • Astudillo, L.1    Gonzalez, A.2    Galindo, A.3    Mansilla, T.4
  • 4
    • 0000556185 scopus 로고
    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1984) Tetrahedron , vol.40 , pp. 4371
    • Hijfte, L.V.1    Vandewalle, M.2
  • 5
    • 0026496907 scopus 로고
    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1992) Tetrahedron , vol.48 , pp. 9789
    • Carda, M.1    Marco, J.A.2
  • 6
    • 0001136112 scopus 로고
    • For representative examples, see: (a) Flegel, M.; Adam, K.-L.; Becker, H. Phytochemistry 1999, 52, 1633; (b) Finnegan, R. A.; Djerassi, C. J. Am. Chem. Soc. 1960, 82, 4342; (c) Astudillo, L.; Gonzalez, A.; Galindo, A.; Mansilla, T. Tetrahedron Lett. 1997, 38, 6737; (d) Hijfte, L. V.; Vandewalle, M. Tetrahedron 1984, 40, 4371; (e) Carda, M.; Marco, J. A. Tetrahedron 1992, 48, 9789; (f) Talwar, K. K.; Singh, I. P.; Kalsi, P. S. Phytochemistry 1992, 31, 336.
    • (1992) Phytochemistry , vol.31 , pp. 336
    • Talwar, K.K.1    Singh, I.P.2    Kalsi, P.S.3
  • 16
    • 0000048482 scopus 로고
    • B.M. Trost. Oxford: Pergamon Press
    • . Review article of intramolecular Diels-Alder reaction, see: Roush W.R. Trost B.M., Comprehensive Organic Synthesis. 5:1991;513 Pergamon Press, Oxford.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 513
    • Roush, W.R.1
  • 24
    • 0010646837 scopus 로고    scopus 로고
    • Determination of the ee values of compounds of 16-18 is performed on a Merck Chiralsphere column (diisopropyl ether/hexane=1/15-1/5).
    • Determination of the ee values of compounds of 16-18 is performed on a Merck Chiralsphere column (diisopropyl ether/hexane=1/15-1/5).
  • 25
    • 0010691977 scopus 로고    scopus 로고
    • note
    • 3: C, 71.36; H, 5.61; Found: C, 71.32; H, 5.60%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.