Reversibly photoswitchable nucleosides: Synthesis and photochromic properties of diarylethene-functionalized 7-deazaadenosine derivatives

Journal of the American Chemical Society

Volumn 132, Issue 24, 2010, Pages 8372-8377

  Singer, Marco ^a   Jäschke, Andres ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BUILDING BLOCKES; CLOSED-RING ISOMERS; CONFORMATIONAL CHANGE; CYCLOREVERSION; DESIGN STEPS; DIARYLETHENES; FLUORESCENCE QUENCHERS; FUNCTIONALIZED; MOLECULAR RECOGNITION PROPERTIES; MOLECULAR SWITCHES; NMR MEASUREMENTS; NUCLEOSIDE ANALOGUES; PHOTO-SWITCHABLE; PHOTOCHROMIC PROPERTIES; RING CLOSURES; SPECTRAL PROPERTIES; STRUCTURAL FEATURE; TARGET COMPOUND; THERMALLY STABLE; UV-LIGHT; UV-VIS SPECTROSCOPY; VISIBLE RANGE;

BIOMOLECULES; MOLECULAR RECOGNITION; NUCLEIC ACIDS; OLEFINS; PHOTOCHROMISM; THIOPHENE; ULTRAVIOLET SPECTROSCOPY;

ISOMERS;

ADENOSINE DERIVATIVE; ETHYLENE; NUCLEIC ACID; NUCLEOSIDE; THIOPHENE; THYMIDINE;

ARTICLE; CHEMICAL STRUCTURE; CONFORMATION; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ILLUMINATION; ISOMER; ISOMERIZATION; LIGHT; LIGHT EXPOSURE; MOLECULAR RECOGNITION; PROTON NUCLEAR MAGNETIC RESONANCE; SAMPLE; STIMULUS; SYNTHESIS; ULTRAVIOLET IRRADIATION; ULTRAVIOLET SPECTROSCOPY;

BASE PAIRING; ETHYLENES; LIGHT; PHOTOCHEMICAL PROCESSES; SPECTROPHOTOMETRY, ULTRAVIOLET; TUBERCIDIN;

EID: 77953625911     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja1024782     Document Type: Article

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