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Volumn 58, Issue 43, 2002, Pages 8779-8791

Total synthesis of sphingofungin E from D-glucose derivative

Author keywords

Antifungals; D glucose; Sphingofungin E; Suzuki Miyaura reaction; Total synthesis

Indexed keywords

ANTIFUNGAL AGENT; GLUCOSE DERIVATIVE; SPHINGOFUNGIN E; UNCLASSIFIED DRUG;

EID: 0037152578     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01058-X     Document Type: Article
Times cited : (26)

References (38)
  • 14
  • 22
    • 0032527965 scopus 로고    scopus 로고
    • For total synthesis of sphingofungin F, see: Ref. 2c, (a) Trost B.M., Lee C.B. J. Am. Chem. Soc. 120:1998;6818-6819.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6818-6819
    • Trost, B.M.1    Lee, C.B.2
  • 25
    • 2042507954 scopus 로고
    • For a recent review on the B-alkyl Suzuki-Miyaura cross-coupling reaction, see: (b) Miyaura N., Suzuki A. Chem. Rev. 95:1995;2457.
    • (1995) Chem. Rev. , vol.95 , pp. 2457
    • Miyaura, N.1    Suzuki, A.2
  • 30
    • 0004288922 scopus 로고    scopus 로고
    • S. Hanessian. New York: Marcel Dekker
    • For a review on the synthesis of branched-chain sugars, see: (b) Hanessian S., Preparative Carbohydrate Chemistry. 1997;207-262 Marcel Dekker, New York.
    • (1997) Preparative Carbohydrate Chemistry , pp. 207-262
  • 32
    • 0011243429 scopus 로고    scopus 로고
    • α-Chloroepoxide 12 was obtained as a single diastereomer. The stereochemistry of the newly formed chiral center (α-position of the chloride) was not determined
    • α-Chloroepoxide 12 was obtained as a single diastereomer. The stereochemistry of the newly formed chiral center (α-position of the chloride) was not determined.
  • 36
    • 0011231814 scopus 로고    scopus 로고
    • 3)
    • 3).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.