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Volumn 44, Issue 45, 2003, Pages 8237-8239

A novel and stereospecific synthesis of (+)-exo-brevicomin

Author keywords

exo brevicomin; Internal nucleophile; Sulfinyl moiety

Indexed keywords

ALKENE DERIVATIVE; BREVICOMIN;

EID: 0141888361     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.09.082     Document Type: Article
Times cited : (16)

References (24)
  • 3
    • 0036374838 scopus 로고    scopus 로고
    • For some recent syntheses, refer to: (a) de Sousa, A. L.; Resck, I. S. J. Braz. Chem. Soc. 2002, 13, 233; (b) Mayer, S. F.; Mang, H.; Steinreiber, A.; Saf, R.; Faber, K. Can. J. Chem. 2002, 80, 362; (c) Gallos, J. K.; Kyradjoglou, L. C.; Koftis, T. V. Heterocycles 2001, 55, 781; (d) Burke, S. D.; Muller, N.; Beudry, C. M. Org. Lett. 1999, 1, 1827; (e) Hu, S.; Jayaraman, S.; Oehlschlager, A. C. J. Org. Chem. 1999, 64, 2524.
    • (2002) J. Braz. Chem. Soc. , vol.13 , pp. 233
    • De Sousa, A.L.1    Resck, I.S.2
  • 4
    • 0036240652 scopus 로고    scopus 로고
    • For some recent syntheses, refer to: (a) de Sousa, A. L.; Resck, I. S. J. Braz. Chem. Soc. 2002, 13, 233; (b) Mayer, S. F.; Mang, H.; Steinreiber, A.; Saf, R.; Faber, K. Can. J. Chem. 2002, 80, 362; (c) Gallos, J. K.; Kyradjoglou, L. C.; Koftis, T. V. Heterocycles 2001, 55, 781; (d) Burke, S. D.; Muller, N.; Beudry, C. M. Org. Lett. 1999, 1, 1827; (e) Hu, S.; Jayaraman, S.; Oehlschlager, A. C. J. Org. Chem. 1999, 64, 2524.
    • (2002) Can. J. Chem. , vol.80 , pp. 362
    • Mayer, S.F.1    Mang, H.2    Steinreiber, A.3    Saf, R.4    Faber, K.5
  • 5
    • 0035307197 scopus 로고    scopus 로고
    • For some recent syntheses, refer to: (a) de Sousa, A. L.; Resck, I. S. J. Braz. Chem. Soc. 2002, 13, 233; (b) Mayer, S. F.; Mang, H.; Steinreiber, A.; Saf, R.; Faber, K. Can. J. Chem. 2002, 80, 362; (c) Gallos, J. K.; Kyradjoglou, L. C.; Koftis, T. V. Heterocycles 2001, 55, 781; (d) Burke, S. D.; Muller, N.; Beudry, C. M. Org. Lett. 1999, 1, 1827; (e) Hu, S.; Jayaraman, S.; Oehlschlager, A. C. J. Org. Chem. 1999, 64, 2524.
    • (2001) Heterocycles , vol.55 , pp. 781
    • Gallos, J.K.1    Kyradjoglou, L.C.2    Koftis, T.V.3
  • 6
    • 0033518053 scopus 로고    scopus 로고
    • For some recent syntheses, refer to: (a) de Sousa, A. L.; Resck, I. S. J. Braz. Chem. Soc. 2002, 13, 233; (b) Mayer, S. F.; Mang, H.; Steinreiber, A.; Saf, R.; Faber, K. Can. J. Chem. 2002, 80, 362; (c) Gallos, J. K.; Kyradjoglou, L. C.; Koftis, T. V. Heterocycles 2001, 55, 781; (d) Burke, S. D.; Muller, N.; Beudry, C. M. Org. Lett. 1999, 1, 1827; (e) Hu, S.; Jayaraman, S.; Oehlschlager, A. C. J. Org. Chem. 1999, 64, 2524.
    • (1999) Org. Lett. , vol.1 , pp. 1827
    • Burke, S.D.1    Muller, N.2    Beudry, C.M.3
  • 7
    • 0033515569 scopus 로고    scopus 로고
    • For some recent syntheses, refer to: (a) de Sousa, A. L.; Resck, I. S. J. Braz. Chem. Soc. 2002, 13, 233; (b) Mayer, S. F.; Mang, H.; Steinreiber, A.; Saf, R.; Faber, K. Can. J. Chem. 2002, 80, 362; (c) Gallos, J. K.; Kyradjoglou, L. C.; Koftis, T. V. Heterocycles 2001, 55, 781; (d) Burke, S. D.; Muller, N.; Beudry, C. M. Org. Lett. 1999, 1, 1827; (e) Hu, S.; Jayaraman, S.; Oehlschlager, A. C. J. Org. Chem. 1999, 64, 2524.
    • (1999) J. Org. Chem. , vol.64 , pp. 2524
    • Hu, S.1    Jayaraman, S.2    Oehlschlager, A.C.3
  • 18
    • 85031059325 scopus 로고    scopus 로고
    • The sulfone 9 was prepared in four high yielding steps from ethyl acetoacetate
    • The sulfone 9 was prepared in four high yielding steps from ethyl acetoacetate.
  • 21
    • 85031058271 scopus 로고    scopus 로고
    • 3)
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.