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Volumn 44, Issue 30, 2003, Pages 5625-5628

Synthetic studies directed toward the total synthesis of dolabriferol

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; AMIDE; DOLABRIFEROL; EPOXIDE; LITHIUM DERIVATIVE; NATURAL PRODUCT; UNCLASSIFIED DRUG; ZINC DERIVATIVE;

EID: 0037829746     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01351-0     Document Type: Article
Times cited : (32)

References (32)
  • 3
    • 85031147376 scopus 로고    scopus 로고
    • note
    • The numbering of 1 as well as of each intermediate follows that suggested in Ref. 1.
  • 17
    • 33747849809 scopus 로고    scopus 로고
    • note
    • 2. (a) Gensler, W. J.; Johnson, F.; Sloam, A. D. B. J. Am. Chem. Soc. 1960, 82, 6074; (b) Oishi, T.; Nakata, T. Acc. Chem. Res. 1984, 17, 338; (c) Evans, D. A.; Kim, A. S.; Metternich, R.; Novack, V. J. J. Am. Chem. Soc. 1998, 120, 5921.
  • 18
    • 0025058974 scopus 로고
    • 13C NMR resonances at 19.0, 30.2, and 98.3 are characteristic of a syn acetonide and the large vicinal coupling constants, JHb-Hc=JHc-Hd=10.4 Hz are consistent with the preferred chair conformation. (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945; (b) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099; (c) Rychnovsky, S. D.; Rogers, B. N.; Richardson, T. I. Acc. Chem. Res. 1998, 31, 9.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 945
    • Rychnovsky, S.D.1    Skalitzky, D.J.2
  • 19
    • 0025608552 scopus 로고
    • 13C NMR resonances at 19.0, 30.2, and 98.3 are characteristic of a syn acetonide and the large vicinal coupling constants, JHb-Hc=JHc-Hd=10.4 Hz are consistent with the preferred chair conformation. (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945; (b) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099; (c) Rychnovsky, S. D.; Rogers, B. N.; Richardson, T. I. Acc. Chem. Res. 1998, 31, 9.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7099
    • Evans, D.A.1    Rieger, D.L.2    Gage, J.R.3
  • 20
    • 0001951357 scopus 로고    scopus 로고
    • 13C NMR resonances at 19.0, 30.2, and 98.3 are characteristic of a syn acetonide and the large vicinal coupling constants, JHb-Hc=JHc-Hd=10.4 Hz are consistent with the preferred chair conformation. (a) Rychnovsky, S. D.; Skalitzky, D. J. Tetrahedron Lett. 1990, 31, 945; (b) Evans, D. A.; Rieger, D. L.; Gage, J. R. Tetrahedron Lett. 1990, 31, 7099; (c) Rychnovsky, S. D.; Rogers, B. N.; Richardson, T. I. Acc. Chem. Res. 1998, 31, 9.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 9
    • Rychnovsky, S.D.1    Rogers, B.N.2    Richardson, T.I.3
  • 32
    • 85031146981 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR, HRMS, and analytical data. Yields refer to chromatographically and spectroscopically homogeneous materials.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.