CARBON NUCLEAR MAGNETIC RESONANCE;
CONFERENCE PAPER;
ELECTRON TRANSPORT;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PROTEIN CONFORMATION;
PROTEIN STRUCTURE;
PROTON NUCLEAR MAGNETIC RESONANCE;
RESTRICTION MAPPING;
STEREOCHEMISTRY;
SUBSTITUTION REACTION;
CARBON ISOTOPES;
GUANOSINE;
HYDROGEN;
IMIDAZOLES;
INDICATORS AND REAGENTS;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR CONFORMATION;
NITROGEN;
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
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.
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.
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.
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.
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.
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.