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Theoretical studies on conformational preferences of modified nucleic acid base N6-(N-glycylcarbonyl) adenine

✍ Scribed by Ravindra Tewari

Book ID
104582112
Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
714 KB
Volume
31
Category
Article
ISSN
0020-7608

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πŸ“œ SIMILAR VOLUMES

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Protonation-induced conformational changes are studied in the hypermodified nucleic acid base N6-(N-glycylcarbonyl) adenine, gc6Ade, using the quantum chemical perturbative configuration interaction using localised orbitals method. Protonation at the N(7) position of adenine in gc6Ade induces reorie

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The influence of protonation at N 1 on the conformational preferences Ε½ . 6 Ε½ . of the N 6 substituent in the modified nucleic acid base N -N-glycylcarbonyl adenine, gc 6 Ade, was investigated by the quantum chemical perturbative configuration interaction Ε½ . using localized orbitals PCILO method.

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