메뉴 건너뛰기




Volumn 111, Issue 20, 1989, Pages 7932-7938

Biosynthesis of Antibiotic LL-C 10037α: The Steps beyond 3-Hydroxyanthranilic Acid

Author keywords

[No Author keywords available]

Indexed keywords

BIOSYNTHESIS; CHEMICAL REACTIONS--SYNTHESIS; DEUTERIUM COMPOUNDS; FUNGI; NUCLEAR MAGNETIC RESONANCE;

EID: 0024731071     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00202a039     Document Type: Article
Times cited : (24)

References (54)
  • 3
    • 85022877690 scopus 로고    scopus 로고
    • We have established the correct absolute stereochemistry as shown (unpublished results)
    • We have established the correct absolute stereochemistry as shown (unpublished results).
  • 7
    • 84981760064 scopus 로고
    • These compounds had previously been reported: However, the melting point of the material purported to be 5 was 80 °C lower than that of ours
    • These compounds had previously been reported: Kehrmann, F.; Bahatrian, G. Chem. Ber. 1898, 31, 2399. However, the melting point of the material purported to be 5 was 80 °C lower than that of ours.
    • (1898) Chem. Ber. , vol.31 , pp. 2399
    • Kehrmann, F.1    Bahatrian, G.2
  • 8
    • 0007870133 scopus 로고
    • Olah, G. A.; Narang, S. C.; Gupta, B. G. B.; Malhotra, R. J. Org. Chem. 1979, 44, 1247. Vickery, E. H.; Pahler, L. F.; Eisenbraun, E. J. J. Org. Chem. 1979, 44, 4444
    • Morita, T.; Okamoto, Y.; Sakurai, H. J. Chem. Soc., Chem. Commun. 1978, 874. Olah, G. A.; Narang, S. C.; Gupta, B. G. B.; Malhotra, R. J. Org. Chem. 1979, 44, 1247. Vickery, E. H.; Pahler, L. F.; Eisenbraun, E. J. J. Org. Chem. 1979, 44, 4444.
    • (1978) J. Chem. Soc., Chem. Commun. , pp. 874
    • Morita, T.1    Okamoto, Y.2    Sakurai, H.3
  • 11
    • 85022825123 scopus 로고
    • 5th ed.; Chapman and Hall: London
    • Dictionary of Organic Compounds, 5th ed.; Chapman and Hall: London, 1982; Vol. 1, p 146.
    • (1982) Dictionary of Organic Compounds , vol.1 , pp. 146
  • 34
    • 0021014489 scopus 로고
    • An authentic sample was prepared by oxidation of 1 with pyridinium chlorochromate
    • An authentic sample was prepared by oxidation of 1 with pyridinium chlorochromate: Box, S. J.; Gilpin, M. L.; Gwynn, M.; Hanscomb, G.; Spear, S. R.; Brown, A. G. J. Antibiot. 1983, 36, 1631.
    • (1983) J. Antibiot. , vol.36 , pp. 1631
    • Box, S.J.1    Gilpin, M.L.2    Gwynn, M.3    Hanscomb, G.4    Spear, S.R.5    Brown, A.G.6
  • 37
    • 0019356976 scopus 로고
    • For comprehensive papers, see: Scott, A. I.; Zamir, L.; Phillips, G. T.; Yalpani, M. Bioorg. Chem. 1973, 2, 124
    • For comprehensive papers, see: Neway, J.; Gaucher, G. M. Can. J. Microbiol. 1981, 27, 206. Scott, A. I.; Zamir, L.; Phillips, G. T.; Yalpani, M. Bioorg. Chem. 1973, 2, 124.
    • (1981) Can. J. Microbiol. , vol.27 , pp. 206
    • Neway, J.1    Gaucher, G.M.2
  • 50
    • 83455210966 scopus 로고    scopus 로고
    • 14C]gentisylquinone was incorporated into whole wild-type P. urticae cells. Neither toluquinone nor gentisaldehyde quinone has been fed to fermentations or cell-free extracts of the mutant that accumulates isoepoxydon and phyllostine
    • 14C]gentisylquinone was incorporated into whole wild-type P. urticae cells. Neither toluquinone nor gentisaldehyde quinone has been fed to fermentations or cell-free extracts of the mutant that accumulates isoepoxydon and phyllostine. Gaucher, G. M. Personal communication.
    • Personal communication
    • Gaucher, G.M.1
  • 53
    • 85022742211 scopus 로고    scopus 로고
    • Beilstein Vol. 13, 371.
    • Beilstein , vol.13 , pp. 371
  • 54
    • 85022769845 scopus 로고
    • 5th ed.; Chapman and Hall: London
    • Dictionary of Organic Compounds, 5th ed.; Chapman and Hall: London, 1982; vol. 1, p 304.
    • (1982) Dictionary of Organic Compounds , vol.1 , pp. 304


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.