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Volumn 40, Issue 22, 1999, Pages 4267-4270

Eight membered ethers via diene metathesis: Synthetic approach to laureatin natural products

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE; ETHER DERIVATIVE; LAUREATIN; LAUREATIN DERIVATIVE; NATURAL PRODUCT; RUTHENIUM; UNCLASSIFIED DRUG;

EID: 0033612164     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00703-0     Document Type: Article
Times cited : (68)

References (25)
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    • (1968) Tetrahedron Lett. , pp. 2091-2096
    • Irie, T.1    Izawa, M.2    Kurosawa, E.3
  • 3
    • 0013570110 scopus 로고
    • Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron Lett. 1968, 2091-2096; Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron Lett. 1968, 2735-2738; Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron 1970, 26, 851-870.
    • (1968) Tetrahedron Lett. , pp. 2735-2738
    • Irie, T.1    Izawa, M.2    Kurosawa, E.3
  • 4
    • 0001232749 scopus 로고
    • Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron Lett. 1968, 2091-2096; Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron Lett. 1968, 2735-2738; Irie, T.; Izawa, M.; Kurosawa, E. Tetrahedron 1970, 26, 851-870.
    • (1970) Tetrahedron , vol.26 , pp. 851-870
    • Irie, T.1    Izawa, M.2    Kurosawa, E.3
  • 7
    • 0026042052 scopus 로고
    • Fukuzawa, A.; Takasugi, Y.; Murai, A. Tetrahedron Lett. 1991, 32, 5597-5598; Ishihara, J.; Kanoh, N.; Murai, A. Tetrahedron Lett. 1995, 36, 737-740; Ishihara, J.; Shimada, Y.; Kanoh, N.; Takasugi, Y.; Fukuzawa, A.; Murai. A. Tetrahedron 1997, 53, 8371-8382.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 5597-5598
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  • 8
    • 0028876783 scopus 로고
    • Fukuzawa, A.; Takasugi, Y.; Murai, A. Tetrahedron Lett. 1991, 32, 5597-5598; Ishihara, J.; Kanoh, N.; Murai, A. Tetrahedron Lett. 1995, 36, 737-740; Ishihara, J.; Shimada, Y.; Kanoh, N.; Takasugi, Y.; Fukuzawa, A.; Murai. A. Tetrahedron 1997, 53, 8371-8382.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 737-740
    • Ishihara, J.1    Kanoh, N.2    Murai, A.3
  • 9
    • 0030991887 scopus 로고    scopus 로고
    • Fukuzawa, A.; Takasugi, Y.; Murai, A. Tetrahedron Lett. 1991, 32, 5597-5598; Ishihara, J.; Kanoh, N.; Murai, A. Tetrahedron Lett. 1995, 36, 737-740; Ishihara, J.; Shimada, Y.; Kanoh, N.; Takasugi, Y.; Fukuzawa, A.; Murai. A. Tetrahedron 1997, 53, 8371-8382.
    • (1997) Tetrahedron , vol.53 , pp. 8371-8382
    • Ishihara, J.1    Shimada, Y.2    Kanoh, N.3    Takasugi, Y.4    Fukuzawa, A.5    Murai, A.6
  • 12
    • 0029006233 scopus 로고
    • and references therein
    • Burton, J. W.; Clark, J. S.; Derrer, S.; Stork, T. C.; Bendall, J. G.; Holmes, A. B. J. Am. Chem. Soc. 1997, 119, 7483-7498; Bratz, M.; Bullock, W. H.; Overnnan, L. E.; Takemoto, T. J. Am. Chem. Soc. 1995, 117, 5958 and references therein.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5958
    • Bratz, M.1    Bullock, W.H.2    Ovennan, L.E.3    Takemoto, T.4
  • 14
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    • Kling, M. R.; McNaughlon-Smith, G. A.; Taylor, R. J. K. J. Chem. Soc., Chem. Commun. 1993, 1593-1595; McNaughton-Smith, G. A.; Taylor, R. J. K. Tetrahedron 1996, 52, 2113-2124.
    • (1996) Tetrahedron , vol.52 , pp. 2113-2124
    • McNaughton-Smith, G.A.1    Taylor, R.J.K.2
  • 17
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    • note
    • All new compounds were fully characterised by high field NMR spectroscopy and by elemental analysis and/or HRMS.
  • 18
    • 0013598459 scopus 로고    scopus 로고
    • note
    • Cyclisation precursors (7), (10) and (12) were prepared by standard organometallic and alkylation methodology.
  • 21
    • 0000081509 scopus 로고    scopus 로고
    • Linderman, R. J.; Siedlecki, J.; O'Neill, S. A.; Sun, H. J. Am. Chem. Soc. 1997, 119, 6919-6920; Crimmins, M. T.; Choy, A. L. J. Org. Chem. 1997, 62, 7548-7549.
    • (1997) J. Org. Chem. , vol.62 , pp. 7548-7549
    • Crimmins, M.T.1    Choy, A.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.