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Volumn 2, Issue 8, 2000, Pages 1033-1035

Progress toward synthesis of diazonamide A. Preparation of a 3-(oxazol-5-yl)-4-trifluoromethyl-sulfonyloxyindole and its use in biaryl coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

1 (TERT BUTOXYCARBONYL) 4 TRIFLUOROMETHYLSULFONYLOXY 3 (OXAZOL 5 YL)INDOLE; 1-(TERT-BUTOXYCARBONYL)-4-TRIFLUOROMETHYLSULFONYLOXY-3-(OXAZOL-5-YL)INDOLE; DIAZONAMIDE A; FUSED HETEROCYCLIC RINGS; MESYLIC ACID DERIVATIVE; OXAZOLE DERIVATIVE;

EID: 0034689852     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005548p     Document Type: Article
Times cited : (83)

References (26)
  • 9
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    • (h) Magnus, P.; Kreisberg, J. D. Tetrahedron Lett. 1999, 40, 451. Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 831. Chan, F.; Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 835.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 451
    • Magnus, P.1    Kreisberg, J.D.2
  • 10
    • 0034606908 scopus 로고
    • (h) Magnus, P.; Kreisberg, J. D. Tetrahedron Lett. 1999, 40, 451. Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 831. Chan, F.; Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 835.
    • (1200) Tetrahedron Lett. , vol.41 , pp. 831
    • Magnus, P.1    McIver, E.G.2
  • 11
    • 0034606983 scopus 로고
    • (h) Magnus, P.; Kreisberg, J. D. Tetrahedron Lett. 1999, 40, 451. Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 831. Chan, F.; Magnus, P.; McIver, E. G. Tetrahedron Lett. 1200, 41, 835.
    • (1200) Tetrahedron Lett. , vol.41 , pp. 835
    • Chan, F.1    Magnus, P.2    McIver, E.G.3
  • 16
    • 0003048811 scopus 로고
    • and references therein
    • (c) Iwao, M. Heterocycles 1993, 36, 29 and references therein.
    • (1993) Heterocycles , vol.36 , pp. 29
    • Iwao, M.1
  • 22
    • 2042507954 scopus 로고
    • For a review of Suzuki coupling reactions, see: Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457.
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 23
    • 85037520821 scopus 로고    scopus 로고
    • Structure 6, preceding paper. See ref 3
    • Structure 6, preceding paper. See ref 3.
  • 26
    • 85037513494 scopus 로고    scopus 로고
    • unpublished results
    • According to the method of ref 12b, treatment of the 3-(oxazol-5-yl)indole 24 with 2.15 equiv n-butyllithium in THF/DMPU at -78°C followed by slow addition of N-chlorosuccinimide in dichloromethane and warming to room temperature gave 25 in 60% yield: Vedejs, E.; Zajac, M., unpublished results.
    • Vedejs, E.1    Zajac, M.2


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