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Tetrasubstituted Olefinic Xanthene Dyes: Synthesis via Pd-Catalyzed 6-<i>exo-dig</i> Cyclization/C–H Activation of 2-Bromobenzyl-<i>N</i>-propargylamines and Solid State Fluorescence Properties
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2013
Year
DerivativesEngineeringPhotochemistryAlkene MetathesisNew Xanthene DerivativesInternal RotationDiversity-oriented SynthesisNatural SciencesPhotoredox ProcessSynthetic PhotochemistryOrganic ChemistryCatalysisAggregation StateChemistryHeterocycle ChemistryOlefinic Xanthene DyesEnantioselective SynthesisBiomolecular Engineering
Tetrasubstituted olefin based new xanthene derivatives have been synthesized via palladium-catalyzed carbopalladation/C–H activation of 2-bromobenzyl-N-propargylamine derivatives. The synthesized compounds display a pronounced solid state fluorescence due to their restricted internal rotation of a C–Ar bond in the solid or aggregation state.
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