메뉴 건너뛰기




Volumn 13, Issue 4, 2005, Pages 1231-1238

NMR conformational analysis of p-tolyl furanopyrimidine 2′-deoxyribonucleoside and crystal structure of its 3′,5′-di- O-acetyl derivative

Author keywords

Conformation; Furanopyrimidine; Nucleosides

Indexed keywords

3',5' DI O ACETYL 3 (2' DEOXY BETA DEXTRO RIBOFURANOSYL) 6 (4 METHYLPHENYL) 2,3 DIHYDROFURO[2,3 D]PYRIMIDIN 2 ONE; 4 TOLYLFURANOPYRIMIDINE; ANTIVIRUS AGENT; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 12844286981     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2004.11.013     Document Type: Article
Times cited : (13)

References (62)
  • 7
    • 12844278648 scopus 로고    scopus 로고
    • The Development of C-5 Propyne Oligonucleotides as Inhibitors of Gene Function
    • C.A. Stein A.M. Krieg Wiley-Liss New York
    • M.W. Flanagan, and R.W. Wagner The Development of C-5 Propyne Oligonucleotides as Inhibitors of Gene Function C.A. Stein A.M. Krieg Applied Antisense Oligonucleotide Technology 1998 Wiley-Liss New York 174 191
    • (1998) Applied Antisense Oligonucleotide Technology , pp. 174-191
    • Flanagan, M.W.1    Wagner, R.W.2
  • 37
    • 0002769275 scopus 로고    scopus 로고
    • Cross-coupling Reactions to sp Carbon Atoms
    • F. Sonogashira Diederich P.J. Stang Wiley-VCH Weinheim
    • K. Sonogashira Cross-coupling Reactions to sp Carbon Atoms F. Sonogashira Diederich P.J. Stang Metal-Catalyzed Cross-Coupling Reactions 1998 Wiley-VCH Weinheim 203 230
    • (1998) Metal-Catalyzed Cross-Coupling Reactions , pp. 203-230
    • Sonogashira, K.1
  • 48
    • 9444259952 scopus 로고
    • Numbering of the six-membered ring for furanopyrimidine used in this work differs from the parent pyrimidine (uridine) ring and follows RF 10623: American Chemical Society, Chemical Abstracts Service: Columbus
    • Numbering of the six-membered ring for furanopyrimidine used in this work differs from the parent pyrimidine (uridine) ring and follows RF 10623: Ring Systems Handbook, American Chemical Society, Chemical Abstracts Service: Columbus, 1993; p 498RSF
    • (1993) Ring Systems Handbook
  • 53
    • 12844259463 scopus 로고    scopus 로고
    • note
    • 2 (sin 36°+ sin 72°)
  • 54
    • 12844256356 scopus 로고    scopus 로고
    • note
    • Numbering used in original reference given in parentheses
  • 56
    • 12844256355 scopus 로고    scopus 로고
    • note
    • 13C signals of 88.8 ppm with H-4′ and 88.3 ppm with H-1′ proton
  • 57
    • 12844249358 scopus 로고    scopus 로고
    • note
    • 13C NMR.
  • 58
    • 12844288627 scopus 로고    scopus 로고
    • m/z for most intense peak of isotope envelope
    • m/z for most intense peak of isotope envelope
  • 59
    • 12844287519 scopus 로고    scopus 로고
    • 3 group
    • 3 group
  • 60
    • 0004150157 scopus 로고    scopus 로고
    • University of Göttingen, Germany
    • Sheldrick, G. M. SHELXL-97. University of Göttingen, Germany, 1997
    • (1997) SHELXL-97
    • Sheldrick, G.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.