메뉴 건너뛰기




Volumn 100, Issue 10, 1978, Pages 3208-3212

Stereochemical Studies of Isoprenoid Biosynthesis. Biosynthesis of Fomannosin from [1,2- 13C2] Acetate

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33645248193     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00478a042     Document Type: Article
Times cited : (52)

References (58)
  • 1
    • 0000356672 scopus 로고
    • For recent reviews and leading references see, M. Tanabe
    • For recent reviews and leading references see, M. Tanabe, Biosynthesis, 2, 241-299 (1973).; 3, 247-285 (1974).; 4, 204-247 (1976).
    • (1973) Biosynthesis , vol.2 , pp. 241-299
  • 11
    • 0015883841 scopus 로고
    • For 13C NMR studies of the stereochemistry of (a). β-lactam biosynthesis:
    • For 13C NMR studies of the stereochemistry of (a). β-lactam biosynthesis: N. Neuss, C. H. Nash, J. E. Baldwin, P. A. Lemke, and J. B. Grutzner, J. Am. Chem. Soc., 95, 3797 (1973).;
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 3797
    • Neuss, N.1    Nash, C.H.2    Baldwin, J.E.3    Lemke, P.A.4    Grutzner, J.B.5
  • 18
    • 0016843223 scopus 로고
    • Using 13C NMR: see also ref 4 and 9.
    • Using 13C NMR: D. E. Cane and R. H. Levin, J. Am. Chem. Soc., 97, 1282 (1975).; see also ref 4 and 9.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1282
    • Cane, D.E.1    Levin, R.H.2
  • 28
    • 85023268150 scopus 로고
    • Wissenschaftliche Beitraege von Dozentstripendiaten, Verband der Chemischen Industrie e. V., Eigenverlag, Frankfurt, 1975, p 31, for a similar conclusion based on CD measurements.
    • (1975) , pp. 31
  • 29
    • 84982342025 scopus 로고
    • and references cited therein.
    • H. Gerlach, Heiv. Chim. Acta, 51, 1587 (1968)., and references cited therein.
    • (1968) Heiv. Chim. Acta , vol.51 , pp. 1587
    • Gerlach, H.1
  • 31
    • 0003409299 scopus 로고
    • Carbon-13 Nuclear Magnetic Resonance for Organic Chemists
    • Wiley-lnterscience, New York, N.Y.
    • a). G. C. Levy and G. L. Nelson, “Carbon-13 Nuclear Magnetic Resonance for Organic Chemists”, Wiley-lnterscience, New York, N.Y., 1972;
    • (1972)
    • Levy, G.C.1    Nelson, G.L.2
  • 56
    • 0002116587 scopus 로고
    • For a biogenetically modeled synthesis of hirsutene as well as in vitro studies of humulene oyclizations, cf. Y. Ohfune, H. Shirahama, and T. Matsumoto, Tetrahedron Lett
    • For a biogenetically modeled synthesis of hirsutene as well as in vitro studies of humulene oyclizations, cf. Y. Ohfune, H. Shirahama, and T. Matsumoto, Tetrahedron Lett., 2795 (1976).;
    • (1976) , pp. 2795
  • 57
    • 3042972207 scopus 로고
    • H. linuma, T. Takita, K. Maeda, and H. Umezawa, Tetrahedron Lett.
    • S. Misumi, Y. Ohfune, A. Furusaki, H. Shirahama, and T. Matsumoto, H. linuma, T. Takita, K. Maeda, and H. Umezawa, Tetrahedron Lett., 2865 (1976).;
    • (1976) , pp. 2865
    • Misumi, S.1    Ohfune, Y.2    Furusaki, A.3    Shirahama, H.4    Matsumoto, T.5
  • 58
    • 0001981988 scopus 로고
    • H. linuma, T. Takita, K. Maeda, and H. Umezawa, Tetrahedron Lett.
    • Y. Ohfune, H. Shirahama, and T. Matsumoto, H. linuma, T. Takita, K. Maeda, and H. Umezawa, Tetrahedron Lett., 2869 (1976).
    • (1976) , pp. 2869
    • Ohfune, Y.1    Shirahama, H.2    Matsumoto, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.