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Volumn 6, Issue 8, 1998, Pages 1233-1241

Biomimetic Diels-Alder cyclizations for the construction of the brevianamide, paraherquamide, sclerotamide, asperparaline and VM55599 ring systems

Author keywords

[No Author keywords available]

Indexed keywords

ASPERPARALINE; BICYCLO COMPOUND; BREVIANAMIDE; PARAHERQUAMIDE; SCLEROTAMIDE; UNCLASSIFIED DRUG; VM 55599;

EID: 0031710510     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(98)00102-3     Document Type: Article
Times cited : (55)

References (39)
  • 31
    • 0344899025 scopus 로고    scopus 로고
    • The syn-/anti-relationship refers to the relative stereochemistry between the C-19 stereogenic center (brevianamide numbering) and the cyclic amino acid residue (proline, β-methylproline, or pipecolic acid):
    • The syn-/anti-relationship refers to the relative stereochemistry between the C-19 stereogenic center (brevianamide numbering) and the cyclic amino acid residue (proline, β-methylproline, or pipecolic acid):
  • 34
    • 0342927518 scopus 로고
    • It should be noted that deoxybrevianamide E, the minor isomer from this procedure could be used with equal efficacy in this synthesis.
    • Kametani, T.; Kanaya, N.; Ihara, M. J. Chem. Soc. Perkin Trans. I 1981, 959. It should be noted that deoxybrevianamide E, the minor isomer from this procedure could be used with equal efficacy in this synthesis.
    • (1981) J. Chem. Soc. Perkin Trans. I , pp. 959
    • Kametani, T.1    Kanaya, N.2    Ihara, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.