Supramolecular approach to enantioselective DNA recognition using enantiomerically resolved cationic 4-amino-1,8-naphthalimide-based Tröger's bases

Journal of Organic Chemistry

Volumn 79, Issue 19, 2014, Pages 9272-9283

  Banerjee, Swagata ^a   Bright, Sandra A ^a   Smith, Jayden A ^a   Burgeat, Jeremy ^a   Martinez Calvo, Miguel ^a   Williams, D Clive ^a   Kelly, John M ^a   Gunnlaugsson, Thorfinnur ^a  

^a TRINITY COLLEGE DUBLIN   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; CELL CULTURE; DICHROISM; DNA; ENANTIOMERS; FUNCTIONAL GROUPS; ION EXCHANGE; SPECTROSCOPIC ANALYSIS; VAN DER WAALS FORCES;

CATION EXCHANGE CHROMATOGRAPHY; DOUBLE-HELICAL STRUCTURES; PHOTOPHYSICAL STUDIES; PREFERENTIAL BINDING; SPECTROSCOPIC METHOD; THERMAL DENATURATIONS; VAN DER WAALS INTERACTIONS; VISIBLE-LIGHT IRRADIATION;

X RAY CRYSTALLOGRAPHY;

4 AMINO 1,8 NAPHTHALIMIDE BASED TROGER BASE; BASE; DNA; DOUBLE STRANDED DNA; ETHIDIUM BROMIDE; NAPHTHALIMIDE DERIVATIVE; POLYNUCLEOTIDE; SEPHADEX; UNCLASSIFIED DRUG; 1 NAPHTHYLAMINE; 4-AMINO-1,8-NAPHTHALIMIDE; CATION; QUINOLONE DERIVATIVE;

ABSORPTION; ARTICLE; AT RICH SEQUENCE; CELL VIABILITY; CIRCULAR DICHROISM; CONTROLLED STUDY; DNA BINDING; DNA DENATURATION; ENANTIOMER; ENANTIOSELECTIVITY; ION EXCHANGE CHROMATOGRAPHY; IONIC STRENGTH; LINEAR DICHROISM; MOLECULAR RECOGNITION; RACEMIZATION; SOLID STATE; SPECTROSCOPY; SUPRAMOLECULAR CHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY; ANALOGS AND DERIVATIVES; ANIMAL; BINDING SITE; CELL LINE; CHEMICAL STRUCTURE; CHEMISTRY; DNA CLEAVAGE; HUMAN; LIGHT; NUCLEOTIDE SEQUENCE; PHOTOCHEMISTRY; RADIATION RESPONSE; SALMON; STEREOISOMERISM;

1-NAPHTHYLAMINE; ANIMALS; BASE SEQUENCE; BINDING SITES; CATIONS; CELL LINE; CIRCULAR DICHROISM; CRYSTALLOGRAPHY, X-RAY; DNA; DNA CLEAVAGE; HUMANS; LIGHT; MOLECULAR STRUCTURE; NAPHTHALIMIDES; PHOTOCHEMICAL PROCESSES; QUINOLONES; SALMON; STEREOISOMERISM;

EID: 84907790135     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo501711g     Document Type: Article

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