An efficient strategy for the synthesis of o-((ethyl)aminomethyl) phenyl boronic acid anchored on a BODIPY core is reported. Kinetic studies highlight the association with diols and fructose; BODIPY fluorescence is quenched upon substrate binding, showing an unusual turn-off response.
Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols
MINEO, PLACIDO;
2014-01-01
Abstract
An efficient strategy for the synthesis of o-((ethyl)aminomethyl) phenyl boronic acid anchored on a BODIPY core is reported. Kinetic studies highlight the association with diols and fructose; BODIPY fluorescence is quenched upon substrate binding, showing an unusual turn-off response.File in questo prodotto:
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