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Volumn 39, Issue 16, 1998, Pages 2223-2226

Synthetic studies toward diazonamide A. Preparation of the benzofuranone-indolyloxazole fragment

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; BENZOFURAN DERIVATIVE; DIAZONAMIDE A; UNCLASSIFIED DRUG;

EID: 0032537213     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00231-7     Document Type: Article
Times cited : (71)

References (29)
  • 2
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    • 2. For a partial compilation of other oxazole-containing natural products, see: Wipf, P.; Venkatraman, S. Synlett 1997, 1.
    • (1997) Synlett , pp. 1
    • Wipf, P.1    Venkatraman, S.2
  • 3
    • 0028866791 scopus 로고
    • 3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
    • (1995) J. Am. Chem, Soc. , vol.117 , pp. 558
    • Hennoxazole, A.1    Wipf, P.2    Lim, S.3
  • 4
    • 0001620021 scopus 로고    scopus 로고
    • 3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
    • (1996) Chimia , vol.50 , pp. 157
    • Wipf, P.1    Lim, S.2
  • 5
    • 0029847930 scopus 로고    scopus 로고
    • 3. Hennoxazole A: Wipf, P.; Lim, S. J. Am. Chem, Soc. 1995, 117, 558; Wipf, P.; Lim, S. Chimia 1996, 50, 157. Muscoride A: Wipf, P.; Venkatraman, S. J. Org. Chem. 1996, 61, 6517.
    • (1996) J. Org. Chem. , vol.61 , pp. 6517
    • Muscoride, A.1    Wipf, P.2    Venkatraman, S.3
  • 13
    • 0010730490 scopus 로고    scopus 로고
    • We thank Dr. S. Lim for preliminary studies on the preparation of oxazole 7
    • 9. We thank Dr. S. Lim for preliminary studies on the preparation of oxazole 7.
  • 20
    • 33748647785 scopus 로고
    • (b) de Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. Engl. 1994, 33, 2379. For a related benzofuranone cyclization, see: Anacardio, R.; Arcadi, A.; D'Anniballe, G.; Marinelli, F. Synthesis 1995, 831.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2379
    • De Meijere, A.1    Meyer, F.E.2
  • 22
    • 0010647216 scopus 로고    scopus 로고
    • Enantiomeric excess was determined by chiral HPLC of the O-MTPA-ester or the free alcohol derivative of 12 on a Chiralcel OD column
    • 14. Enantiomeric excess was determined by chiral HPLC of the O-MTPA-ester or the free alcohol derivative of 12 on a Chiralcel OD column.
  • 27
    • 0030972808 scopus 로고    scopus 로고
    • We thank Prof. Shibasaki for a sample of (S)-BINAs
    • 19. Kojima, A.; Boden, C. D. J.; Shibasaki, M. Tetrahedron Lett. 1997, 38, 3459. We thank Prof. Shibasaki for a sample of (S)-BINAs.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 3459
    • Kojima, A.1    Boden, C.D.J.2    Shibasaki, M.3
  • 28
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    • 13C NMR, IR and HRMS
    • 13C NMR, IR and HRMS.
  • 29
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    • 4: (equation presented)
    • 4: (equation presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.