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Volumn 61, Issue 1, 1996, Pages 2-3

Independent generation and reactivity of 2′-deoxyurid-1′-yl

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYURIDINE DERIVATIVE;

EID: 0030032563     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951769a     Document Type: Article
Times cited : (56)

References (22)
  • 14
    • 85033840021 scopus 로고    scopus 로고
    • note
    • 2O. This is attributed to a cationic rearrangement.
  • 15
    • 85033851726 scopus 로고    scopus 로고
    • Unpublished results, Colorado State University
    • Yoo, D. J.; Greenberg, M. M. Unpublished results, Colorado State University.
    • Yoo, D.J.1    Greenberg, M.M.2
  • 16
    • 0004344770 scopus 로고
    • The Benjamin/Cummings Publishing Co., Inc.: Menlo Park, CA, and references therein
    • Turro, N. J. Modern Molecular Photochemistry, The Benjamin/Cummings Publishing Co., Inc.: Menlo Park, CA, 1978; and references therein.
    • (1978) Modern Molecular Photochemistry
    • Turro, N.J.1
  • 17
    • 85033860730 scopus 로고    scopus 로고
    • note
    • Photolyses in the presence of cyclohexa-1,4-diene were carried out in a mixture of acetonitrile and water (3:2 by volume).
  • 19
    • 85033854899 scopus 로고    scopus 로고
    • note
    • Uracil and 2′-deoxyuridine were quantitated by reversed phase HPLC. 2′-Deoxjribonolactone was quantitated as its bis(trimethylsilyl) ether via GC/MS using selected ion monitoring. Response factors versus appropriate internal standards were measured for each product


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