Ghent University Academic Bibliography

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De novo enantioselective synthesis of hexafluorinated D-glucose

Sébastien Depienne (UGent) , Clément Q. Fontenelle, Mark E. Light, Kristof Van Hecke (UGent) and Bruno Linclau (UGent)

(2024) JOURNAL OF ORGANIC CHEMISTRY. 89(19). p.14291-14304
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Conformational analysis of 1,3-difluorinated alkanes

William G. Poole, Florent Peron, Stephen J. Fox, Neil Wells, Chris-Kriton Skylaris, Jonathan W. Essex, Ilya Kuprov and Bruno Linclau (UGent)

(2024) JOURNAL OF ORGANIC CHEMISTRY. 89(12). p.8789-8803
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Obtaining pure 1H NMR spectra of individual pyranose and furanose anomers of reducing deoxyfluorinated sugars

Gabija Poskaite, David E. Wheatley, Neil Wells, Bruno Linclau (UGent) and Davy Sinnaeve

(2023) JOURNAL OF ORGANIC CHEMISTRY. 88(19). p.13908-13925
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Suzuki-Miyaura cross-coupling of amides by N-C cleavage mediated by air-stable, well-defined [Pd(NHC)(sulfide)Cl2] catalysts : reaction development, scope, and mechanism

Shiyi Yang, Xiang Yu, Yaxu Liu, Michele Tomasini, Lucia Caporaso, Albert Poater, Luigi Cavallo, Catherine Cazin (UGent) , Steven Nolan (UGent) and Michal Szostak

(2023) JOURNAL OF ORGANIC CHEMISTRY. 88(15). p.10858-10868
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Dithioallyl cations in stereoselective dearomative (3 + 2) cycloadditions of benzofurans : mechanism and synthetic applications

Bram Ryckaert (UGent) , Jan Hullaert, Kristof Van Hecke (UGent) and Johan Winne (UGent)

(2023) JOURNAL OF ORGANIC CHEMISTRY. 88(20). p.14504-14514
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Azolium aurates as pre-catalysts for the oxidative coupling of terminal alkynes under mild conditions

Xinyuan Ma, Nikolaos Tzouras, Min Peng (UGent) , Kristof Van Hecke (UGent) and Steven Nolan (UGent)

(2022) JOURNAL OF ORGANIC CHEMISTRY. 87(7). p.4883-4893
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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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Skipped fluorination motifs : synthesis of building blocks and comparison of lipophilicity trends with vicinal and isolated fluorination motifs

Robert Troup, Benjamin Jeffries, Raphael El-Bekri Saudain, Eleni Georgiou, Johanna Fish, James S. Scott, Elisabetta Chiarparin, Charlene Fallan and Bruno Linclau (UGent)

(2021) JOURNAL OF ORGANIC CHEMISTRY. 86(2). p.1882-1900
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Stereodivergent synthesis of biologically active spironucleoside scaffolds via catalytic cyclopropanation of 4-exo-methylene furanosides

Zeina Neouchy (UGent) , Jonas Verhoeven, Hanchu Kong, Yongbin Zhao, Wenbin Wang, Marta Brambilla, Kristof Van Hecke (UGent) , Lieven Meerpoel, Jan Willem Thuring, Guido Verniest, et al.

(2021) JOURNAL OF ORGANIC CHEMISTRY. 86(23). p.17344-17361
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Synthesis of 2,3,4-trideoxy-2,3,4-trifluoroglucose

Lucas Quiquempoix, Zhong Wang, Jerome Graton, Peter G. Latchem, Mark Light, Jean-Yves Le Questel and Bruno Linclau (UGent)

(2019) JOURNAL OF ORGANIC CHEMISTRY. 84(9). p.5899-5906

Academic Bibliography

De novo enantioselective synthesis of hexafluorinated D-glucose

Conformational analysis of 1,3-difluorinated alkanes

Obtaining pure 1H NMR spectra of individual pyranose and furanose anomers of reducing deoxyfluorinated sugars

Suzuki-Miyaura cross-coupling of amides by N-C cleavage mediated by air-stable, well-defined [Pd(NHC)(sulfide)Cl2] catalysts : reaction development, scope, and mechanism

Dithioallyl cations in stereoselective dearomative (3 + 2) cycloadditions of benzofurans : mechanism and synthetic applications

Azolium aurates as pre-catalysts for the oxidative coupling of terminal alkynes under mild conditions

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

Skipped fluorination motifs : synthesis of building blocks and comparison of lipophilicity trends with vicinal and isolated fluorination motifs

Stereodivergent synthesis of biologically active spironucleoside scaffolds via catalytic cyclopropanation of 4-exo-methylene furanosides

Synthesis of 2,3,4-trideoxy-2,3,4-trifluoroglucose

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