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Volumn 55, Issue 16, 1999, Pages 4999-5016

Synthetic studies on the starfish alkaloid imbricatine. A chiral synthesis of tri-O-methylimbricatine

Author keywords

Amino acids and derivatives; Imidazoles imidazolidinones; Isoquinolines; Thioethers

Indexed keywords

ALKALOID; BENZAMIDE DERIVATIVE; BENZENE DERIVATIVE; BENZYLTETRAHYDROISOQUINOLINE; IMBRICATINE; ISOQUINOLINE DERIVATIVE; METHYLAMINE; PYRAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033574468     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00199-4     Document Type: Article
Times cited : (22)

References (34)
  • 13
    • 0013524723 scopus 로고    scopus 로고
    • 3
    • 3.
  • 17
    • 0000939490 scopus 로고
    • Noland, W. E., Ed.; John Wiley & Sons Inc.: New York
    • (b) Lipton, M. F.; Basha, A.; Weinreb, S. M. Organic Syntheses Coll. Vol. 6; Noland, W. E., Ed.; John Wiley & Sons Inc.: New York, 1988; pp. 492-495.
    • (1988) Organic Syntheses Coll. , vol.6 , pp. 492-495
    • Lipton, M.F.1    Basha, A.2    Weinreb, S.M.3
  • 18
    • 37049071641 scopus 로고
    • 2) containing the tertiary amide as directed metalation group (DMG) failed to provide the desired product 20, although lithiation of the benzyl ether analogue bearing the oxazoline DMG at the same position is known to proceed and to give the corresponding ester on treatment with ethyl chloroformate: Kennedy, M; Moody, C. J.; Rees, C. W.; Vaquera, J. J. J. Chem. Soc., Perkin Trans. 1 1987, 1395-1398.
    • (1987) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1395-1398
    • Kennedy, M.1    Moody, C.J.2    Rees, C.W.3    Vaquera, J.J.4
  • 25
  • 29
    • 0013544125 scopus 로고    scopus 로고
    • For convenience, each position of the 4-methoxyphenyl ring or the 4-benzyloxyphenyl ring is indicated by a primed number
    • For convenience, each position of the 4-methoxyphenyl ring or the 4-benzyloxyphenyl ring is indicated by a primed number.
  • 31
    • 0013491972 scopus 로고    scopus 로고
    • A Merck-Schuchardt product was purchased through Kanto Chemical Co. (Japan) and purified by vacuum distillation before use
    • A Merck-Schuchardt product was purchased through Kanto Chemical Co. (Japan) and purified by vacuum distillation before use.
  • 32
    • 0013551863 scopus 로고    scopus 로고
    • For convenience, each aromatic carbon in the tetrasubstituted phenyl moiety is indicated by a primed number; that in the 4-methoxyphenyl moiety, by a double-primed number
    • For convenience, each aromatic carbon in the tetrasubstituted phenyl moiety is indicated by a primed number; that in the 4-methoxyphenyl moiety, by a double-primed number.
  • 34
    • 0013492336 scopus 로고    scopus 로고
    • For convenience, each skeletal atom in the histidine moiety is indicated by a primed number; each aromatic carbon in the 4-methoxyphenyl moiety, by a double-primed number
    • For convenience, each skeletal atom in the histidine moiety is indicated by a primed number; each aromatic carbon in the 4-methoxyphenyl moiety, by a double-primed number.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.