Solution Conformational Characteristics of Chemically Modified Purine(β)Pentosides
暂无分享,去创建一个
[1] W. Olson. How flexible is the furanose ring? 2. An updated potential energy estimate , 1982 .
[2] M. J. Robins,et al. Arabinose Conformations of 9-β -ᴅ-Arabinofuranosyladenine (ARA-A) Analogues Modified at the 2',3' or 5' Positions , 1980 .
[3] M. J. Robins,et al. Xylose Conformations of 9-β-ᴅ-Xylofuranosyladenine Analogues Modified at the 2'3' or 5'-Positions and Lyxose Conformations of 9-β-ᴅ-Lyxofuranosyladenine , 1980 .
[4] M. J. Robins,et al. Ribose Conformations of Adenosine Analogs Modified at the 2', 3' or 5' Positions , 1979 .
[5] I. Ekiel,et al. Correlations of conformational parameters and equilibrium conformational states in a variety of beta-D-arabinonucleosides and their analogues. , 1979, Biochimica et biophysica acta.
[6] I. Ekiel,et al. Coupling constants between cisoidal protons in pentose nucleosides. Limitations of range of application of Karplus relation, and solution conformations of .beta.-arabinofuranosyl and .beta.-xylofuranosyl nucleosides , 1978 .
[7] I. Ekiel,et al. Solution conformation and relative acidities of the sugar hydroxyls of the O'-methylated derivates of the antimetabolite 9-beta-D-xylofuranosyladenine. , 1978, Biochemistry.
[8] E. Westhof,et al. Solution conformational analysis of 2'-amino-2''deoxyadenosine, 3'-amino-3'-deoxyadenosine and puromycin by pulsed nuclear-magnetic-resonance methods. , 1977, European journal of biochemistry.
[9] E. Westhof,et al. Proton magnetic resonance studies of 2'-,3'-, and 5'-deoxyadenosine conformations in solution. , 1977, Nucleic acids research.
[10] A. Bloch. Chemistry, biology, and clinical uses of nucleoside analogs , 1975 .
[11] E. Westhof,et al. A dynamic correlation between ribose conformation and glycosyl torsion angle of dissolved xanthosine studies by continuous-wave-mode and pulsed nuclear-magnetic-resonance methods. , 1974, European Journal of Biochemistry.
[12] M. Sundaralingam,et al. Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation. , 1972, Journal of the American Chemical Society.
[13] F. Hruska,et al. A nuclear magnetic resonance study of the molecular conformation of beta-pseudouridine in aqueous solution. , 1970, Journal of the American Chemical Society.