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Volumn 40, Issue 15, 1999, Pages 3063-3066

Studies on the total synthesis of the saponaceolides. 1. Enantioselective synthesis of the spiroketal subunit

Author keywords

Fungi; Natural products; Spiro compounds; Terpenoids

Indexed keywords

ACETAL; DIKETONE; NATURAL PRODUCT; PYRAN DERIVATIVE; SAPONACEOLIDE; SPIRO COMPOUND; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033537820     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00366-4     Document Type: Article
Times cited : (13)

References (17)
  • 9
    • 0013547986 scopus 로고    scopus 로고
    • note
    • 2), 75.0 (C-O), 76.1 (CH-O), 78.2 (C-O), 120.4 (CH), 120.6 (CH), 125.5 (CH), 125.7 (CH), 126.1 (CH), 126.3 (CH), 128.7 (CH), 132.3 (C), 134.1 (C), 141.0 C), 154.9 (C=O), 204.3 CH)
  • 13
    • 0013514323 scopus 로고    scopus 로고
    • note
    • Yields refer to homogeneous compounds fully characterized by analytical and spectroscopic data.
  • 14
    • 0000610844 scopus 로고
    • and references cited therein
    • Kishi Y. Pure Appl. Chem. 1992;64:343-350 and references cited therein.
    • (1992) Pure Appl. Chem. , vol.64 , pp. 343-350
    • Kishi, Y.1
  • 17
    • 0013506046 scopus 로고    scopus 로고
    • note
    • 2O), 72.6 (C-O), 77.5 (C-O), 96.8 (C-O), 100.8 (C-O), 127.8 (2 CH), 129.8 (2 CH), 132.7 (C), 144.8 (C).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.