Fluorogenic Transformations Based on Formation of CC Bonds Catalyzed by Palladium: An Efficient Approach for High Throughput Optimizations and Kinetic Studies

We have developed novel fluorogenic transformations based on formation of CC bonds catalyzed by palladium using iodocoumarin 1 as a model aryl iodide, where fluorescence is quenched completely due to effects of the heavy, polarizable iodine atom. Substitution of the iodine atom for the carbon using...

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Bibliographic Details
Published inAdvanced synthesis & catalysis Vol. 350; no. 1; pp. 71 - 75
Main Authors Rozhkov, Roman V., Davisson, V. Jo, Bergstrom, Donald E.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 04.01.2008
WILEY‐VCH Verlag
Wiley
Subjects
Chemistry
Chemistry, Applied
Chemistry, Organic
CC coupling
fluorescence
homogeneous catalysis
palladium
Physical Sciences
Science & Technology
C-C coupling
DESIGN
ASSAY
ARYLATION
LIBRARY
LIGATION
RESONANCE ENERGY-TRANSFER
SENSORS
homogeneous catalysis
fluorescence
COUPLING REACTIONS
CHEMISTRY
palladium
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Summary:We have developed novel fluorogenic transformations based on formation of CC bonds catalyzed by palladium using iodocoumarin 1 as a model aryl iodide, where fluorescence is quenched completely due to effects of the heavy, polarizable iodine atom. Substitution of the iodine atom for the carbon using Sonogashira, Suzuki–Miyaura and Heck couplings results in a dramatic fluorescence enhancement. This approach has been used successfully for the optimization of reaction conditions and kinetic studies in high throughput format.
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ISSN:1615-4150
1615-4169
DOI:10.1002/adsc.200700384