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Issue 83, 2014
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Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols

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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.

Graphical abstract: Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols

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Supplementary files

Article information


Submitted
06 Aug 2014
Accepted
10 Sep 2014
First published
16 Sep 2014

RSC Adv., 2014,4, 43931-43933
Article type
Communication

Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols

M. Cordaro, P. Mineo, F. Nastasi and G. Magazzù, RSC Adv., 2014, 4, 43931 DOI: 10.1039/C4RA08213C

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