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Volumn 44, Issue 37, 2003, Pages 7055-7059

A general, ring closure metathesis based enantiospecific approach to polyfunctional eudesmane, eremophilane and agarofuran sesquiterpenoids

Author keywords

[No Author keywords available]

Indexed keywords

AGAROFURAN DERIVATIVE; CARVONE; EREMOPHILANE DERIVATIVE; EUDESMANE DERIVATIVE; SESQUITERPENOID;

EID: 0041565402     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01757-X     Document Type: Article
Times cited : (34)

References (23)
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    • Reviews: (a) Fraga, B. M. Nat. Prod. Rep. 2002, 19, 650-672 and earlier contributions by the same author in this review series. (b) Faulkner, D. J. Nat. Prod. Rep. 2002, 19, 1-48 and earlier contributions by the same author in this review series.
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    • Selected examples of agarofuran natural products, see: (a) Maheshwari, M. L.; Jain, T. C.; Bates, R. B.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1079-1090; (b) Maheshwari, M. L.; Varma, K. R.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1519-1525; (c) Bruning, R.; Wagner, H. Phytochemistry 1978, 17, 1821-1858; (d) Kim, S. E.; Kim, Y. H.; Lee, J. J. J. Nat. Prod. 1998, 61, 108-111.
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    • Selected examples of agarofuran natural products, see: (a) Maheshwari, M. L.; Jain, T. C.; Bates, R. B.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1079-1090; (b) Maheshwari, M. L.; Varma, K. R.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1519-1525; (c) Bruning, R.; Wagner, H. Phytochemistry 1978, 17, 1821-1858; (d) Kim, S. E.; Kim, Y. H.; Lee, J. J. J. Nat. Prod. 1998, 61, 108-111.
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    • Selected examples of agarofuran natural products, see: (a) Maheshwari, M. L.; Jain, T. C.; Bates, R. B.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1079-1090; (b) Maheshwari, M. L.; Varma, K. R.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1519-1525; (c) Bruning, R.; Wagner, H. Phytochemistry 1978, 17, 1821-1858; (d) Kim, S. E.; Kim, Y. H.; Lee, J. J. J. Nat. Prod. 1998, 61, 108-111.
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    • Selected examples of agarofuran natural products, see: (a) Maheshwari, M. L.; Jain, T. C.; Bates, R. B.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1079-1090; (b) Maheshwari, M. L.; Varma, K. R.; Bhattacharyya, S. C. Tetrahedron 1963, 19, 1519-1525; (c) Bruning, R.; Wagner, H. Phytochemistry 1978, 17, 1821-1858; (d) Kim, S. E.; Kim, Y. H.; Lee, J. J. J. Nat. Prod. 1998, 61, 108-111.
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    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
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    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
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    • Tu, Y.Q.1    Sun, L.D.2
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    • 0035938347 scopus 로고    scopus 로고
    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3101-3103
    • Zhou, G.1    Gao, X.2    Li, W.Z.3    Li, Y.4
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    • 0035804410 scopus 로고    scopus 로고
    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 769-771
    • Spivey, A.C.1    Woodhead, S.J.2    Weston, M.3    Andrews, B.I.4
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    • 0037148002 scopus 로고    scopus 로고
    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 627-630
    • Xia, W.J.1    Li, D.R.2    Shi, L.3    Tu, Y.Q.4
  • 17
    • 0037064516 scopus 로고    scopus 로고
    • and earlier papers by this group
    • For some recent references towards the synthesis of agarofurans: (a) White, J. D.; Shin, H.; Kim, T.-S.; Cutshall, N. S. J. Am. Chem. Soc. 1997, 119, 2404-2419; (b) Tu, Y. Q.; Sun, L. D. Tetrahedron Lett. 1998, 39, 7935-7938; (c) Zhou, G.; Gao, X.; Li, W. Z.; Li, Y. Tetrahedron Lett. 2001, 42, 3101-3103 and earlier contributions of this group; (d) Spivey, A. C.; Woodhead, S. J.; Weston, M.; Andrews, B. I. Angew. Chem., Int. Ed. 2001, 40, 769-771; (e) Xia, W. J.; Li, D. R.; Shi, L.; Tu, Y. Q. Tetrahedron Lett. 2002, 43, 627-630; (f) Boyer, F.-D.; Descoins, C. L.; Descoins, C.; Prange, T.; Ducrot, P.-H. Tetrahedron Lett. 2002, 43, 8277-8279 and earlier papers by this group.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 8277-8279
    • Boyer, F.-D.1    Descoins, C.L.2    Descoins, C.3    Prange, T.4    Ducrot, P.-H.5
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    • note
    • abstract
  • 23
    • 85031142966 scopus 로고    scopus 로고
    • note
    • abstract


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.