Selective boronic acid fluorescent sensors for saccharide detection

Boronic acids in orgamc chemistry are extensively used as building blocks in coupling reactions. Moreover, boronic acids also act as Lewis acids which enable them to easily form reversible covalent complexes with sugars, amino acids and other Lewis base donors. Taking this unique characteristic that...

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Main Author: Wang, Hui-Chen
Published: University of Bath 2012
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582865
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5828652015-03-20T05:21:15ZSelective boronic acid fluorescent sensors for saccharide detectionWang, Hui-Chen2012Boronic acids in orgamc chemistry are extensively used as building blocks in coupling reactions. Moreover, boronic acids also act as Lewis acids which enable them to easily form reversible covalent complexes with sugars, amino acids and other Lewis base donors. Taking this unique characteristic that two phenylboronic acids separated by a six-carbon amino linker are especially selective for D-glucose. The major part of this research is to modify boronic acid sensors with various fluorophores and material supports, not just for saccharide detection, but also for other applications such as protein / peptide separation in electrophoresis or surface plasmon resonance analysis. Saccharides also form glycoconjugates which are involved in cell-cell recognition / interactions in biological systems; therefore, the development of new boronic acid fluorescent sensors for bioimaging is also included within the research.547.037University of Bathhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582865Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 547.037
spellingShingle 547.037
Wang, Hui-Chen
Selective boronic acid fluorescent sensors for saccharide detection
description Boronic acids in orgamc chemistry are extensively used as building blocks in coupling reactions. Moreover, boronic acids also act as Lewis acids which enable them to easily form reversible covalent complexes with sugars, amino acids and other Lewis base donors. Taking this unique characteristic that two phenylboronic acids separated by a six-carbon amino linker are especially selective for D-glucose. The major part of this research is to modify boronic acid sensors with various fluorophores and material supports, not just for saccharide detection, but also for other applications such as protein / peptide separation in electrophoresis or surface plasmon resonance analysis. Saccharides also form glycoconjugates which are involved in cell-cell recognition / interactions in biological systems; therefore, the development of new boronic acid fluorescent sensors for bioimaging is also included within the research.
author Wang, Hui-Chen
author_facet Wang, Hui-Chen
author_sort Wang, Hui-Chen
title Selective boronic acid fluorescent sensors for saccharide detection
title_short Selective boronic acid fluorescent sensors for saccharide detection
title_full Selective boronic acid fluorescent sensors for saccharide detection
title_fullStr Selective boronic acid fluorescent sensors for saccharide detection
title_full_unstemmed Selective boronic acid fluorescent sensors for saccharide detection
title_sort selective boronic acid fluorescent sensors for saccharide detection
publisher University of Bath
publishDate 2012
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582865
work_keys_str_mv AT wanghuichen selectiveboronicacidfluorescentsensorsforsaccharidedetection
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