Ghent University Academic Bibliography

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- Journal Article
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Synthesis of 4‐imidoyl‐, 4‐oxiranyl‐ and 4‐propargyloxyphenyl‐substituted β‐lactam building blocks

Sari Deketelaere (UGent) , Gurkirat Kaur (UGent) , Nicola Piens, Daan Deturck, Robin Depestel, Kristof Van Hecke (UGent) , Christian Stevens (UGent) , Vipan Kumar and Matthias D'hooghe (UGent)

(2023) JOURNAL OF HETEROCYCLIC CHEMISTRY. 60(3). p.423-430
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Practical ferrioxalate actinometry for the determination of photon fluxes in production-oriented photoflow reactors

Bavo Vandekerckhove (UGent) , Nicola Piens, Bert Metten, Christian Stevens (UGent) and Thomas Heugebaert (UGent)

(2022) ORGANIC PROCESS RESEARCH & DEVELOPMENT. 26(8). p.2392-2402
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Reactivity of 3-oxo-β-lactams with respect to primary amines

Sari Deketelaere (UGent) , Nicola Piens, Hannelore Goossens (UGent) , Dietmar Hertsen, Lieselotte Crul, Lotte Demeurisse, Jelle De Moor, Elias Van Den Broeck (UGent) , Karen Mollet (UGent) , Kristof Van Hecke (UGent) , et al.

(2019) 18th International Conference on Heterocycles in Bioorganic Chemistry, Abstracts.
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Reactivity of 3-oxo-β-lactams with respect to primary amines

Sari Deketelaere (UGent) , Nicola Piens, Hannelore Goossens (UGent) , Dietmar Hertsen, Lieselotte Crul, Lotte Demeurisse, Jelle De Moor, Elias Van Den Broeck (UGent) , Karen Mollet (UGent) , Kristof Van Hecke (UGent) , et al.

(2019) 2nd Chemical Research in Flanders, Abstracts.
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- Journal Article
- A1
- open access
Chemoenzymatic approach toward the synthesis of 3-O-(α/β)-glucosylated 3-hydroxy-β-lactams

Lena Decuyper, Jorick Franceus (UGent) , Shari Dhaene (UGent) , Maarten Debruyne (UGent) , Kevin Vandoorne, Nicola Piens, Griet Dewitte, Tom Desmet (UGent) and Matthias D'hooghe (UGent)

(2018) ACS OMEGA. 3(11). p.15235-15245
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- PhD Thesis
- open access
Synthesis of new β-lactam building blocks and their application in heterocyclic chemistry

Nicola Piens

(2017)
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- Journal Article
- A1
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Carbonylation of aziridines as a powerful tool for the synthesis of functionalized β-lactams

Nicola Piens and Matthias D'hooghe (UGent)

(2017) EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 40. p.5943-5960
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Cobalt carbonyl-catalyzed carbonylation of functionalized aziridines to versatile β-lactam building blocks

Nicola Piens, Kristof Van Hecke (UGent) , Dieter Vogt and Matthias D'hooghe (UGent)

(2017) ORGANIC & BIOMOLECULAR CHEMISTRY. 15(22). p.4816-4821
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Use of α,ω-dichloroketimine building blocks for the construction of 1-azabicyclo[3.1.0]hexanes, piperidines, pyridines, pyrroles and tetrahydroindoles

Nicola Piens, Wim Aelterman, Matthias D'hooghe (UGent) and Norbert De Kimpe (UGent)

(2017) SYNLETT. 28(2). p.207-213
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- Journal Article
- A1
- open access
Reactivity of 3-oxo-β-lactams with respect to primary amines : an experimental and computational approach

Nicola Piens, Hannelore Goossens (UGent) , Dietmar Hertsen, Sari Deketelaere (UGent) , Lieselotte Crul, Lotte Demeurisse, Jelle De Moor, Elias Van Den Broeck (UGent) , Karen Mollet (UGent) , Kristof Van Hecke (UGent) , et al.

(2017) CHEMISTRY-A EUROPEAN JOURNAL. 23(71). p.18002-18009

Academic Bibliography

Synthesis of 4‐imidoyl‐, 4‐oxiranyl‐ and 4‐propargyloxyphenyl‐substituted β‐lactam building blocks

Practical ferrioxalate actinometry for the determination of photon fluxes in production-oriented photoflow reactors

Reactivity of 3-oxo-β-lactams with respect to primary amines

Reactivity of 3-oxo-β-lactams with respect to primary amines

Chemoenzymatic approach toward the synthesis of 3-O-(α/β)-glucosylated 3-hydroxy-β-lactams

Synthesis of new β-lactam building blocks and their application in heterocyclic chemistry

Carbonylation of aziridines as a powerful tool for the synthesis of functionalized β-lactams

Cobalt carbonyl-catalyzed carbonylation of functionalized aziridines to versatile β-lactam building blocks

Use of α,ω-dichloroketimine building blocks for the construction of 1-azabicyclo[3.1.0]hexanes, piperidines, pyridines, pyrroles and tetrahydroindoles

Reactivity of 3-oxo-β-lactams with respect to primary amines : an experimental and computational approach

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