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Volumn 39, Issue 18, 1998, Pages 2861-2864

A concise total synthesis of (+)-curacin A, a novel cyclopropyl- substituted thiazoline from the cyanobacterium Lyngbya majuscula

Author keywords

[No Author keywords available]

Indexed keywords

CURACIN A; THIAZOLE DERIVATIVE;

EID: 0032580414     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00318-9     Document Type: Article
Times cited : (36)

References (26)
  • 3
    • 0029014405 scopus 로고
    • 3. For the first synthesis of curacin A and assignment of absolute stereochemistry see: White, J. D.; Kim, T -S. and Nambu, M. J. Am. Chem. Soc., 1995, 117, 5612-5613 and J. Am. Chem. Soc., 1997, 119, 103-111.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5612-5613
    • White, J.D.1    Kim, T.-S.2    Nambu, M.3
  • 4
    • 0031055522 scopus 로고    scopus 로고
    • 3. For the first synthesis of curacin A and assignment of absolute stereochemistry see: White, J. D.; Kim, T -S. and Nambu, M. J. Am. Chem. Soc., 1995, 117, 5612-5613 and J. Am. Chem. Soc., 1997, 119, 103-111.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 103-111
  • 5
  • 6
    • 0030749388 scopus 로고    scopus 로고
    • 4. (a) Hoemann, M. Z.; Agrios, K. A.; Aubé, J. Tetrahedron Lett., 1996, 37, 953-956; Hoemann, M. Z.; Agrios, K. A.; Aubé, J. Tetrahedron, 1997, 53, 11087-11098;
    • (1997) Tetrahedron , vol.53 , pp. 11087-11098
    • Hoemann, M.Z.1    Agrios, K.A.2    Aubé, J.3
  • 7
  • 8
  • 10
    • 0030580437 scopus 로고    scopus 로고
    • (c) Onoda, T.; Shirai, R.; Koiso, Y.; Iwasaki, S. Tetrahedron Lett., 1996, 37, 4397-4400; Onoda, T.; Shirai, R.; Koiso, Y.; Iwasaki, S. Tetrahedron, 1996, 52, 14543-14562;
    • (1996) Tetrahedron , vol.52 , pp. 14543-14562
    • Onoda, T.1    Shirai, R.2    Koiso, Y.3    Iwasaki, S.4
  • 13
    • 0029160613 scopus 로고
    • 5. For our contemporaneous applications of this approach to thiazoline-based cyclopeptides see: Boden, C. D. J.; Pattenden, G. Tetrahedron Lett., 1995, 36, 6153-6156; Boden, C. D. J.; Norley, M. C.; Pattenden, G. Tetrahedron Lett., 1996, 37, 9111-9114.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6153-6156
    • Boden, C.D.J.1    Pattenden, G.2
  • 14
    • 0030577467 scopus 로고    scopus 로고
    • 5. For our contemporaneous applications of this approach to thiazoline-based cyclopeptides see: Boden, C. D. J.; Pattenden, G. Tetrahedron Lett., 1995, 36, 6153-6156; Boden, C. D. J.; Norley, M. C.; Pattenden, G. Tetrahedron Lett., 1996, 37, 9111-9114.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 9111-9114
    • Boden, C.D.J.1    Norley, M.C.2    Pattenden, G.3
  • 17
    • 0010683115 scopus 로고    scopus 로고
    • note
    • 8. All compounds showed satisfactory spectroscopic data and microanalytical and/or mass spectrometry data.
  • 19
    • 0003161893 scopus 로고
    • 10. Garner, P.; Park, J. M. Organic Syntheses, 1992, 70, 18-26; McKillop, A.; Taylor, R. J. K.; Watson, R. J.; Lewis, N. Synthesis, 1994, 1, 31-33.
    • (1992) Organic Syntheses , vol.70 , pp. 18-26
    • Garner, P.1    Park, J.M.2
  • 23
    • 0027367957 scopus 로고
    • and references cited Hierein
    • 13. See for example: (a) Zacharie, B.; Sauvé, G.; Penney, C. Tetrahedron, 1993, 49, 10489-10500 and references cited Hierein;
    • (1993) Tetrahedron , vol.49 , pp. 10489-10500
    • Zacharie, B.1    Sauvé, G.2    Penney, C.3
  • 25
    • 0027955980 scopus 로고
    • 14. Wipf, P.; Fritch, P. C. Tetrahedron Lett., 1994, 35, 5397-5400; Atkins, G. M. Jr ; Burgess, E. M. J. Am. Chem. Soc., 1968, 90, 4744-4745.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 5397-5400
    • Wipf, P.1    Fritch, P.C.2
  • 26


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.