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Spectrochimica Acta - Part A Molecular and Biomolecular Spectroscopy

Volumn 57, Issue 1, 2001, Pages 55-72

Quantum chemistry predicted correlations between geometric isomerism (conformation) of -OH and =NH substituents and typical group frequencies of nucleic acid bases: Cytosine

(2) Ha, T K a Gunthard, H H a

a ETH ZURICH (Switzerland)

Author keywords

Cytosine; Group mode frequencies; Hydroxy and imino substituents

Indexed keywords

ADENINE; CYTOSINE; DRUG DERIVATIVE; GUANINE; ISOCYTOSINE; URACIL; XANTHINE;

ARTICLE; CALORIMETRY; CHEMICAL STRUCTURE; CHEMISTRY; CONFORMATION; ISOMERISM; QUANTUM THEORY;

ADENINE; CALORIMETRY; CYTOSINE; GUANINE; ISOMERISM; MODELS, MOLECULAR; MOLECULAR CONFORMATION; QUANTUM THEORY; URACIL; XANTHINE;

CONFORMATIONS; ELECTRIC FIELDS; ISOMERS; MOLECULAR STRUCTURE; NUCLEIC ACIDS; PERTURBATION TECHNIQUES; QUANTUM THEORY; RELAXATION PROCESSES; VECTORS;

CYTOSINE; QUANTUM CHEMISTRY;

NITROGEN COMPOUNDS;

EID: 0034742781 PISSN: 13861425 EISSN: None Source Type: Journal
DOI: 10.1016/S1386-1425(00)00332-2 Document Type: Article

Times cited : (5)

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