A5089951341- Radical Photochemical Reactions
- Chemical Synthesis and Analysis
- Advanced Photocatalysis Techniques
- Catalytic Cross-Coupling Reactions
- Advanced biosensing and bioanalysis techniques
- Crystallization and Solubility Studies
- Chemical Synthesis and Reactions
- Porphyrin and Phthalocyanine Chemistry
- Organic Electronics and Photovoltaics
- Innovative Microfluidic and Catalytic Techniques Innovation
- X-ray Diffraction in Crystallography
- Ammonia Synthesis and Nitrogen Reduction
- Photochromic and Fluorescence Chemistry
- Catalytic C–H Functionalization Methods
University of Amsterdam
2024
Chalmers University of Technology
2019
Abstract Unnatural amino acids, and their synthesis by the late‐stage functionalization (LSF) of peptides, play a crucial role in areas such as drug design discovery. Historically, LSF biomolecules has predominantly utilized traditional synthetic methodologies that exploit nucleophilic residues, cysteine, lysine or tyrosine. Herein, we present photocatalytic hydroarylation process targeting electrophilic residue dehydroalanine (Dha). This possesses an α , β ‐unsaturated moiety can be...
Devices that can capture and convert sunlight into stored chemical energy are attractive candidates for future technologies. A general challenge is to combine efficient solar with high densities storage time a processable composite device application. Here, norbornadiene (NBD)-quadricyclane (QC) molecular photoswitches embedded polymer matrices, possible applications in storing coatings. The NBD-QC capable of absorbing estimated efficiencies up 3.8% combined 0.48 MJ kg
The development of robust and reliable methods for the construction C(sp
Abstract Unnatural amino acids, and their synthesis by the late‐stage functionalization (LSF) of peptides, play a crucial role in areas such as drug design discovery. Historically, LSF biomolecules has predominantly utilized traditional synthetic methodologies that exploit nucleophilic residues, cysteine, lysine or tyrosine. Herein, we present photocatalytic hydroarylation process targeting electrophilic residue dehydroalanine (Dha). This possesses an α , β ‐unsaturated moiety can be...
The development of robust and reliable methods for the construction C(sp2)–C(sp3) bonds is vital accessing an increased array structurally diverse scaffolds in drug discovery campaigns. While significant advances towards this goal have been achieved using metallaphotoredox chemistry, many these utilise photocatalysts based on precious-metals due to their efficient redox processes tuneable properties. However, cost, scarcity, toxicity metals, search suitable replacements should be a priority....
Unnatural amino acids, and their synthesis via the late-stage functionalization (LSF) of peptides, play a crucial role in areas such as drug design discovery. Historically, LSF biomolecules has predominantly utilized traditional synthetic methodologies that exploit nucleophilic residues, cysteine, lysine or tyrosine. In this study, we present photocatalytic hydroarylation process targeting electrophilic residue dehydroalanine (Dha). This possesses an α,β-unsaturated moiety can be combined...
Abstract The development of robust and reliable methods for the construction C(sp 2 )−C(sp 3 ) bonds is vital accessing an increased array structurally diverse scaffolds in drug discovery campaigns. While significant advances towards this goal have been achieved using metallaphotoredox chemistry, many these utilise photocatalysts based on precious‐metals due to their efficient redox processes tuneable properties. However, cost, scarcity, toxicity metals, search suitable replacements should...