Base-base recognition of nonionic dinucleotide analogues in an apolar environment studied by low-temperature NMR spectroscopy

Journal of the American Chemical Society

Volumn 132, Issue 11, 2010, Pages 3862-3869

  Xiao, Zhou ^a,b   Weisz, Klaus ^a  

^a UNIVERSITY OF GREIFSWALD   (Germany)

^b NANYANG TECHNOLOGICAL UNIVERSITY   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

APROTIC; APROTIC SOLVENTS; AQUEOUS ENVIRONMENT; BENZ[C]ACRIDINE; DINUCLEOTIDE DUPLEX; DINUCLEOTIDES; FOLDED STRUCTURES; FREE ENERGY OF BINDING; GLYCOSIDIC TORSION ANGLES; HOOGSTEEN DUPLEX; HYDROPHOBIC EFFECT; INTERCALATORS; LOW TEMPERATURES; NMR SPECTROSCOPY; NO BINDING; NON-AQUEOUS; NONIONIC; POLYCYCLIC AROMATICS; SECONDARY STRUCTURES; SOLVENT MIXTURES; STACKING INTERACTION; STRUCTURAL CHARACTERIZATION; SUGAR PUCKER; VAN DER WAALS; WATSON-CRICK BASE PAIRING;

BINDING ENERGY; BIOMOLECULES; COMPLEXATION; HYDROGEN BONDS; HYDROPHOBICITY; NUCLEAR MAGNETIC RESONANCE; SILICON; SUGAR (SUCROSE); VAN DER WAALS FORCES;

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;

ACRIDINE DERIVATIVE; ANTHRACENE DERIVATIVE; DINUCLEOTIDE;

ARTICLE; CHEMICAL INTERACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; COOLING; CROSS LINKING; ENVIRONMENTAL TEMPERATURE; HETERONUCLEAR MULTIPLE BOND CORRELATION; HYDROGEN BOND; HYDROPHOBICITY; INTERCALATION COMPLEX; LOW TEMPERATURE; MOLECULAR RECOGNITION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

DNA; HYDROGEN BONDING; LIGANDS; MAGNETIC RESONANCE SPECTROSCOPY; MUTAGENS; NUCLEOTIDES; POLYCYCLIC COMPOUNDS; SOLVENTS; TEMPERATURE;

EID: 77949866601     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910220s     Document Type: Article

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