Ghent University Academic Bibliography

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Quantitative analysis of 2D EXSY NMR spectra of strongly coupled spin systems in transmembrane exchange

Dmitry Shishmarev, Clement Q. Fontenelle, Bruno Linclau (UGent) , Ilya Kuprov and Philip W. Kuchel

(2024) CHEMBIOCHEM. 25(3).
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Synthesis and structural characteristics of all mono- and difluorinated 4,6-dideoxy-D-xylo-hexopyranoses

David E. Wheatley, Clement Q. Fontenelle, Ramakrishna Kuppala, Robert Szpera, Edward L. Briggs, Jean-Baptiste Vendeville, Neil J. Wells, Mark E. Light and Bruno Linclau (UGent)

(2021) JOURNAL OF ORGANIC CHEMISTRY. 86(11). p.7725-7756
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Rapid screening of diverse biotransformations for enzyme evolution

Emily E. Kempa, James L. Galman, Fabio Parmeggiani, James R. Marshall, Julien Malassis, Clement Q. Fontenelle, Jean-Baptiste Vendeville, Bruno Linclau (UGent) , Simon J. Charnock, Sabine L. Flitsch, et al.

(2021) JACS AU. 1(4). p.508-516
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Anomerisation of fluorinated sugars by mutarotase studied using F-19 NMR two-dimensional exchange spectroscopy

Dmitry Shishmarev, Lucas Quiquempoix, Clement Q. Fontenelle, Bruno Linclau (UGent) and Philip W. Kuchel

(2020) AUSTRALIAN JOURNAL OF CHEMISTRY. 73(2-3). p.117-128
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Review of mutarotase in 'metabolic subculture' and analytical biochemistry : prelude to F-19 NMR studies of its substrate specificity and mechanism

Dmitry Shishmarev, Lucas Quiquempoix, Clement Q. Fontenelle, Bruno Linclau (UGent) and Philip W. Kuchel

(2020) AUSTRALIAN JOURNAL OF CHEMISTRY. 73(2-3). p.112-116
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Profiling substrate promiscuity of wild-type sugar kinases for multi-fluorinated monosaccharides

Tessa Keenan, Fabio Parmeggiani, Julien Malassis, Clement Q. Fontenelle, Jean-Baptiste Vendeville, Wendy Offen, Peter Both, Kun Huang, Andrea Marchesi, Alex Heyam, et al.

(2020) CELL CHEMICAL BIOLOGY. 27(9). p.1199-1206
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Transmembrane exchange of fluorosugars : characterization of red cell GLUT1 kinetics using( 19)F NMR

Dmitry Shishmarev, Clement Q. Fontenelle, Ilya Kuprov, Bruno Linclau (UGent) and Philip W. Kuchel

(2018) BIOPHYSICAL JOURNAL. 115(10). p.1906-1919
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Investigating the influence of (deoxy) fluorination on the lipophilicity of non-UV-active fluorinated alkanols and carbohydrates by a new log P determination method

Bruno Linclau (UGent) , Zhong Wang, Guillaume Compain, Vincent Paumelle, Clement Q. Fontenelle, Neil Wells and Alex Weymouth-Wilson

(2016) ANGEWANDTE CHEMIE-INTERNATIONAL EDITION. 55(2). p.674-678
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Enantioselective synthesis of dideoxy-tetrafluorinated hexoses

Samuel Golten, Clement Q. Fontenelle, Roxana S. Timofte, Laura Bailac, Mark Light, Muriel Sebban, Hassan Oulyadi and Bruno Linclau (UGent)

(2016) JOURNAL OF ORGANIC CHEMISTRY. 81(11). p.4434-4453
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Intramolecular OH⋅⋅⋅fluorine hydrogen bonding in saturated, acyclic fluorohydrins : the γ-fluoropropanol motif

Bruno Linclau (UGent) , Florent Peron, Elena Bogdan, Neil Wells, Zhong Wang, Guillaume Compain, Clement Q. Fontenelle, Nicolas Galland, Jean-Yves Le Questel and Jerome Graton

(2015) CHEMISTRY-A EUROPEAN JOURNAL. 21(49). p.17808-17816

Academic Bibliography

Quantitative analysis of 2D EXSY NMR spectra of strongly coupled spin systems in transmembrane exchange

Synthesis and structural characteristics of all mono- and difluorinated 4,6-dideoxy-D-xylo-hexopyranoses

Rapid screening of diverse biotransformations for enzyme evolution

Anomerisation of fluorinated sugars by mutarotase studied using F-19 NMR two-dimensional exchange spectroscopy

Review of mutarotase in 'metabolic subculture' and analytical biochemistry : prelude to F-19 NMR studies of its substrate specificity and mechanism

Profiling substrate promiscuity of wild-type sugar kinases for multi-fluorinated monosaccharides

Transmembrane exchange of fluorosugars : characterization of red cell GLUT1 kinetics using( 19)F NMR

Investigating the influence of (deoxy) fluorination on the lipophilicity of non-UV-active fluorinated alkanols and carbohydrates by a new log P determination method

Enantioselective synthesis of dideoxy-tetrafluorinated hexoses

Intramolecular OH⋅⋅⋅fluorine hydrogen bonding in saturated, acyclic fluorohydrins : the γ-fluoropropanol motif

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