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Volumn 22, Issue 5-8, 2003, Pages 1669-1672

Conformationally restricted 2-substituted wyosine derivatives. 1H, 13C, and 15N NMR study

Author keywords

North conformation preference; Restricted conformation 1H, 13C, 15N NMR study; Wyosine derivatives

Indexed keywords

4,9 DIHYDRO 4,6 DIMETHYL 9 OXO 3 (2',3',5' TRI O ACETYL BETA DEXTRO RIBOFURANOSYL) IMIDAZO[1,2 A]PURINE; IMIDAZOLE DERIVATIVE; PURINE DERIVATIVE; SUGAR; UNCLASSIFIED DRUG;

EID: 0141819114     PISSN: 15257770     EISSN: None     Source Type: Journal    
DOI: 10.1081/NCN-120023109     Document Type: Conference Paper
Times cited : (3)

References (10)
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    • de Leeuw, H.P.M.; Hasnoot, C.A.G.; Altona, C. Empirical correlations between conformational parameters in β-D-furanoside fragments derived from a statistical survey of crystal structures of nucleic acid constituents. Full description of nucleoside molecular geometries in terms of four parameters. Isr. J. Chem. 1980, 20, 108-126.
    • (1980) Isr. J. Chem. , vol.20 , pp. 108-126
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  • 2
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    • Hoffmann, R.A.; van Wijk, I.; Leeflang, B.R.; Kamerling, J.P.; Altona, C.; Vliegenthart, J.F.G. Conformational analysis of the α -L-arabinofuranosides present in wheat arabinoxylans from proton-proton coupling constants. J. Am. Chem. Soc. 1992, 114, 3710-3714.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 3710-3714
    • Hoffmann, R.A.1    Van Wijk, I.2    Leeflang, B.R.3    Kamerling, J.P.4    Altona, C.5    Vliegenthart, J.F.G.6
  • 4
    • 0015511563 scopus 로고
    • Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation
    • Altona, C.; Sundaralingam, M. Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation. J. Am. Chem. Soc. 1972, 94, 8205-8212.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 8205-8212
    • Altona, C.1    Sundaralingam, M.2
  • 5
    • 0015913888 scopus 로고
    • Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constants
    • Altona, C.; Sundaralingam, M. Conformational analysis of the sugar ring in nucleosides and nucleotides. Improved method for the interpretation of proton magnetic resonance coupling constants. J. Am. Chem. Soc. 1973, 95, 2333-2344.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 2333-2344
    • Altona, C.1    Sundaralingam, M.2
  • 6
    • 0001120142 scopus 로고
    • How do the gauche and anomeric effect drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides?
    • Plavec, J.; Tong, W.; Chattopadhyaya, J. How do the gauche and anomeric effect drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides? J. Am. Chem. Soc. 1993, 115, 9734-9746.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 9734-9746
    • Plavec, J.1    Tong, W.2    Chattopadhyaya, J.3
  • 7
    • 0027942479 scopus 로고
    • Quantitation of the anomeric effect in adenosine and guanosine by comparison of the thermodynamics of the pseudorotational equilibrium of the pentofuranose moiety in N- and C-nucleosides
    • Thibaudeau, C.; Plavec, J.; Chattopadhyaya, J. Quantitation of the anomeric effect in adenosine and guanosine by comparison of the thermodynamics of the pseudorotational equilibrium of the pentofuranose moiety in N- and C-nucleosides. J. Am. Chem. Soc. 1994, 116, 8033-8037.
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  • 10
    • 84989070934 scopus 로고
    • Structure and conformation of hypermodified purine nucleoside. Wyosine and its isomers: A comparison of coupling constants and distance geometry solutions
    • Sierzputowska-Gracz, H.; Guenther, R.H.; Agris, P.F.; Folkman, W.; Golankiewicz, B. Structure and conformation of hypermodified purine nucleoside. Wyosine and its isomers: A comparison of coupling constants and distance geometry solutions. Magn. Reson. Chem. 1991, 29, 885-892.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.