메뉴 건너뛰기




Volumn 41, Issue 1, 1988, Pages 53-67

NMR studies of chromomycins, olivomycins, and their derivatives

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOMYCIN; CHROMOMYCIN A3; OLIVOMYCIN; OLIVOMYCIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0023848920     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.7164/antibiotics.41.53     Document Type: Article
Times cited : (28)

References (20)
  • 1
    • 0014771246 scopus 로고
    • The stereochemistry of antibiotics of the aureolic acid group
    • Berlin, Yu. A.; M. N. Kolosov & L. A. Piotrovich: The stereochemistry of antibiotics of the aureolic acid group. Tetrahedron Lett. 1970: 1329~1331, 1970.
    • (1970) Tetrahedron Lett. , vol.1970 , pp. 1329-1331
    • Berlin, Y.A.1    Kolosov, M.N.2    Piotrovich, L.A.3
  • 3
    • 84982427347 scopus 로고
    • Olivomycin and related antibiotics
    • Structure of olivomycins A, B, C and D.
    • Berlin, Yu. A.; S. E. Epipov & M. N. Kolosov: Olivomycin and related antibiotics. XVIII. Structure of olivomycins A, B, C and D. Khim. Prir. Soedin 5: 567~572, 1969.
    • (1969) Khim. Prir. Soedin , vol.5 , Issue.18 , pp. 567-572
    • Berlin, Y.A.1    Epipov, S.E.2    Kolosov, M.N.3
  • 4
    • 84915860501 scopus 로고
    • Chem. Abstr. 73: 25823r, 1970.
    • (1970) Chem. Abstr. , vol.73 , pp. 25823r
  • 5
    • 0142208141 scopus 로고
    • Studies on the structure of chromomycin A3 by 1H and 13C nuclear magnetic resonance spectroscopy
    • Thiem, J. & B. Meyer: Studies on the structure of chromomycin A3 by 1H and 13C nuclear magnetic resonance spectroscopy. J. Chem. Soc. Perkin Trans. II 1979: 1331~1336, 1979.
    • (1979) J. Chem. Soc. Perkin Trans. , vol.1979 , Issue.2 , pp. 1331-1336
    • Thiem, J.1    Meyer, B.2
  • 6
    • 0019435186 scopus 로고
    • Studies on the structure of olivomycin A and mithramycin by 1H and 13C nuclear magnetic resonance spectroscopy
    • Thiem, J. & B. Meyer: Studies on the structure of olivomycin A and mithramycin by 1H and 13C nuclear magnetic resonance spectroscopy. Tetrahedron 37: 551~558, 1981.
    • (1981) Tetrahedron , vol.37 , pp. 551-558
    • Thiem, J.1    Meyer, B.2
  • 7
    • 0020355935 scopus 로고
    • Circular dichroic method for determining the position of glycosidic linkage of deoxy sugar moieties antitumor antibiotic chromomycin A3
    • Riccio, R. & K. Nakanishi: Circular dichroic method for determining the position of glycosidic linkage of deoxy sugar moieties antitumor antibiotic chromomycin A3. J. Org. Chem. 47: 4589~4592, 1982.
    • (1982) J. Org. Chem. , vol.47 , pp. 4589-4592
    • Riccio, R.1    Nakanishi, K.2
  • 9
    • 0014668302 scopus 로고
    • A method for Determining the chirality of two aromatic chromophores and the absolute configurations of chromomycin A3 and related antibiotics
    • Harada, N.; K. Nakanishi & S. Tatsuoka: A method for Determining the chirality of two aromatic chromophores and the absolute configurations of chromomycin A3 and related antibiotics. J. Am. Chem. Soc. 91:5896~5898, 1969.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 5896-5898
    • Harada, N.1    Nakanishi, K.2    Tatsuoka, S.3
  • 10
    • 0023868480 scopus 로고
    • New aureolic acid antibiotics
    • Screening, isolation, characterization and biological properties.
    • Koenuma, M.; N. Uchida, K. Yamaguchi, Y. Kawamura & K. Matsumoto: New aureolic acid antibiotics. I. Screening, isolation, characterization and biological properties. J. Antibiotics 41: 45~52, 1988.
    • (1988) J. Antibiotics , vol.41 , Issue.1 , pp. 45-52
    • Koenuma, M.1    Uchida, N.2    Yamaguchi, K.3    Kawamura, Y.4    Matsumoto, K.5
  • 11
    • 0023870398 scopus 로고
    • New aureolic acid antibiotics
    • Structure determination.
    • Koenuma, M.; Y. Yoshimura, K. Matsumoto & Y. Terui: New aureolic acid antibiotics. II. Structure determination. J. Antibiotics 41: 68~72, 1988.
    • (1988) J. Antibiotics , vol.41 , Issue.2 , pp. 68-72
    • Koenuma, M.1    Yoshimura, Y.2    Matsumoto, K.3    Terui, Y.4
  • 12
    • 42049122153 scopus 로고
    • Carbon-13 chemical shifts of isoprenoid-β-D-glucopyranosides and -β-o-mannopyranosides
    • Stereochemical influences of aglycone alcohols.
    • Kasai, R.; M. Suzuo, J. Asakawa & O. Tanaka: Carbon-13 chemical shifts of isoprenoid-β-D-glucopyranosides and -β-o-mannopyranosides. Stereochemical influences of aglycone alcohols. Tetrahedron Lett. 1977: 175~178, 1977.
    • (1977) Tetrahedron Lett. , vol.1977 , pp. 175-178
    • Kasai, R.1    Suzuo, M.2    Asakawa, J.3    Tanaka, O.4
  • 13
    • 33947094112 scopus 로고    scopus 로고
    • Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy
    • (errata; 102: 2512 & 7618, 1980)
    • Seo, S.; Y. Tomita, K. Tori & Y. Yoshimura: Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in carbon-13 nuclear magnetic resonance spectroscopy. J. Am. Chem. Soc. 100: 3331~3339, 1978 (errata; 102: 2512 & 7618, 1980).
    • J. Am. Chem. Soc. , vol.100 , pp. 3331-3339
    • Seo, S.1    Tomita, Y.2    Tori, K.3    Yoshimura, Y.4
  • 14
    • 0001616433 scopus 로고
    • Nuclear magnetic resonance spectroscopy
    • Carbon-13 spectra of some common oligosaccharides.
    • Dorman, D. E. & J. D. Roberts: Nuclear magnetic resonance spectroscopy. Carbon-13 spectra of some common oligosaccharides. J. Am. Chem. Soc. 93: 4463 ~ 4472, 1971.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 4463-4472
    • Dorman, D.E.1    Roberts, J.D.2
  • 15
    • 0018855811 scopus 로고
    • Preparation and antitumor activity of olivomycin A analogues
    • Kumar, V.; W. A. Remers & W. T. Bradner: Preparation and antitumor activity of olivomycin A analogues. J. Med. Chem. 23: 376~379, 1980.
    • (1980) J. Med. Chem. , vol.23 , pp. 376-379
    • Kumar, V.1    Remers, W.A.2    Bradner, W.T.3
  • 16
    • 0001029349 scopus 로고
    • Esterification shifts in carbon-13 NMR spectra of alcohols
    • Terui, Y.; K. Tori & N. Tsuji: Esterification shifts in carbon-13 NMR spectra of alcohols. Tetrahedron Lett. 1976: 621~622, 1976.
    • (1976) Tetrahedron Lett. , vol.1976 , pp. 621-622
    • Terui, Y.1    Tori, K.2    Tsuji, N.3
  • 17
    • 0001310099 scopus 로고
    • Carbon-13 magnetic resonance
    • Steric perturbation of the carbon-13 chemical shift.
    • Grant, D. M. & B. V. Cheney: Carbon-13 magnetic resonance. VII. Steric perturbation of the carbon-13 chemical shift. J. Am. Chem. Soc. 89: 5315~5318, 1967.
    • (1967) J. Am. Chem. Soc. , vol.89 , Issue.7 , pp. 5315-5318
    • Grant, D.M.1    Cheney, B.V.2
  • 18
    • 0001215056 scopus 로고
    • A reinterpretation of beta, gamma, and delta substituent effect on 13C chemical shift
    • Beierbeck, H. & J. K. Saunders: A reinterpretation of beta, gamma, and delta substituent effect on 13C chemical shift. Can. J. Chem. 54: 2985~2995, 1976.
    • (1976) Can. J. Chem. , vol.54 , pp. 2985-2995
    • Beierbeck, H.1    Saunders, J.K.2
  • 19
    • 49549161249 scopus 로고
    • Separable contribution of induction and polarization to the chemical shift
    • Symmetrical, saturated hydrocarbons having no internal rotation
    • Boaz, H.: Separable contribution of induction and polarization to the chemical shift. I. Symmetrical, saturated hydrocarbons having no internal rotation. Tetrahedron Lett. 1973: 55~58, 1973.
    • (1973) Tetrahedron Lett. , Issue.1 , pp. 55-58
    • Boaz, H.1
  • 20
    • 0001490896 scopus 로고
    • The conformational properties of glycosidic linkages
    • Lemieux, R. U. & S. Koto: The conformational properties of glycosidic linkages. Tetrahedron 30: 1933~1944, 1974.
    • (1974) Tetrahedron , vol.30 , pp. 1933-1944
    • Lemieux, R.U.1    Koto, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.