Morgan Regnier

ORCID: 0000-0003-0946-1084
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About
Contact & Profiles
Research Areas
  • Surfactants and Colloidal Systems
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Lipid Membrane Structure and Behavior
  • Water Quality Monitoring Technologies
  • Electrostatics and Colloid Interactions
  • Nanopore and Nanochannel Transport Studies
  • Advanced Polymer Synthesis and Characterization
  • Dendrimers and Hyperbranched Polymers
  • Enhanced Oil Recovery Techniques
  • Microfluidic and Bio-sensing Technologies
  • Advanced biosensing and bioanalysis techniques
  • RNA Interference and Gene Delivery
  • Cyclopropane Reaction Mechanisms
  • Protein Structure and Dynamics
  • Catalytic C–H Functionalization Methods
  • Molecular spectroscopy and chirality
  • Spectroscopy and Quantum Chemical Studies
  • Wastewater Treatment and Nitrogen Removal
  • Membrane Separation Technologies
  • Catalytic Cross-Coupling Reactions
  • CO2 Reduction Techniques and Catalysts
  • Heat Transfer and Boiling Studies
  • Chemical Synthesis and Reactions
  • Electrochemical Analysis and Applications
  • Oxidative Organic Chemistry Reactions

Centrum Wiskunde & Informatica
2025

University of Amsterdam
2023-2025

Novartis (Switzerland)
2021-2024

University of Helsinki
2023-2024

Université de Montpellier
2021

Centre National de la Recherche Scientifique
2021

A sustainable C(sp 2 )–C(sp 3 ) cross-electrophile coupling was developed between readily available 5-bromophthalide and 1-benzyl-4-iodopiperidine under micellar conditions, leading to a key intermediate of one our development compounds.

10.1039/d3cc05916b article EN Chemical Communications 2024-01-01

Peptides or proteins containing small biomolecular aggregates, such as micelles, bicelles, droplets and nanodiscs, are pivotal in many fields ranging from structural biology to pharmaceutics. Monitoring dynamics of systems has been limited by the lack experimental methods that could directly detect their fast (picosecond nanosecond) timescale dynamics. Spin relaxation times NMR experiments sensitive motions, but interpretation for aggregates is not straightforward. Here we show dynamic...

10.1038/s42004-024-01115-4 article EN cc-by Communications Chemistry 2024-02-13

Abstract Cyclopropanes are valuable motifs in organic synthesis, widely featured pharmaceuticals and functional materials. Herein, we report an efficient electrochemical methodology for the cyclopropanation of alkenes, leveraging a nickel‐catalyzed process continuous‐flow. The developed protocol demonstrates broad substrate scope, accommodating both electron‐rich electron‐poor alkenes with high group tolerance. Beyond dichloromethane as feedstock methylene source, enables synthesis...

10.1002/anie.202500203 article EN cc-by Angewandte Chemie International Edition 2025-01-31

Cyclopropanes are valuable motifs in organic synthesis, widely featured pharmaceuticals and functional materials. Herein, we report an efficient electrochemical methodology for the cyclopropanation of alkenes, leveraging a nickel‐catalyzed process continuous‐flow. The developed protocol demonstrates broad substrate scope, accommodating both electron‐rich electron‐poor alkenes with high group tolerance. Beyond dichloromethane as feedstock methylene source, enables synthesis methylated,...

10.1002/ange.202500203 article EN Angewandte Chemie 2025-01-30

We report a metallaphotocatalytic strategy for the selective methylation of (hetero)aryl bromides via nickel-catalyzed cross-coupling with bis(trimethylaluminum)-1,4-diazabicyclo[2.2.2]octane (DABAl-Me₃), as commercially available, air-stable, and non-pyrophoric aluminum-based reagent. The method enables fast, robust, scalable protocol that broadly accommodates various functional groups while preventing protodehalogenation. Mechanistic studies confirm unprecedented generation methyl radicals...

10.26434/chemrxiv-2025-fv54r preprint EN cc-by 2025-03-21

Abstract A practical electrochemical method for synthesizing aryliminophosphoranes from widely available nitro(hetero)arenes in a continuous‐flow system is presented. The utilization of flow technology offers several advantages to our approach, including the elimination need supporting electrolyte and enhanced scalability. Our demonstrates good tolerance towards various functional groups, with electron‐deficient nitroarenes being particularly suitable this strategy. In addition, we have...

10.1002/adsc.202300635 article EN cc-by Advanced Synthesis & Catalysis 2023-07-28

A robust and sustainable C(sp<sup>2</sup>)–C(sp<sup>3</sup>) cross-electrophile coupling was developed <italic>via</italic> nickel/copper synergistic catalysis under micellar conditions.

10.1039/d1cc02885e article EN Chemical Communications 2021-01-01

Cyclic oxyterpenes are natural products that mostly used as fragrances, flavours and drugs by the cosmetic, food pharmaceutical industries. However, only a few cyclic accessible via chemical syntheses, which far from being ecofriendly. We report here synthesis of six derived ß-pinene while respecting principles green sustainable chemistry. Only or biosourced catalysts were in mild conditions optimised for each synthesis. A new generation ecocatalysts, Mn-rich water lettuce, was prepared...

10.3390/molecules26237194 article EN cc-by Molecules 2021-11-27

10.1109/fleps61194.2024.10603875 article EN 2022 IEEE International Conference on Flexible and Printable Sensors and Systems (FLEPS) 2024-06-30

Cyclopropanes are valuable motifs in organic synthesis, widely featured pharmaceuticals and functional materials. Herein, we report an efficient electrochemical methodology for the cyclopropanation of alkenes, leveraging a nickel-catalyzed process continuous-flow. The developed protocol demonstrates broad substrate scope, accommodating both electron-rich electron-poor alkenes with high group tolerance. Beyond dichloromethane as feedstock methylene source, enables synthesis methylated,...

10.26434/chemrxiv-2024-hvqtz preprint EN cc-by 2024-12-11

Dynamic interactions between peptides and lipid membranes are crucial in many biological processes biomedical applications However, monitoring of peptide dynamics a membrane environment has been limited by the lack experimental methods that could directly detect fast (picosecond to nanosecond) timescale this environment. Spin relaxation times from nuclear magnetic resonance (NMR) experiments sensitive such motions, but their often complications sample preparation interpretation data. Here we...

10.26434/chemrxiv-2023-684br preprint EN cc-by 2023-08-21
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