Frank Glorius
Researcher Next ID · RN-027673
Researcher · Chemistry
Münster, Germany
- Works count
- 1,291
- Citation count
- 87,060
- H-index
- 157
- i10-index
- 572
Research interests
Publications
Photocatalytic Late-Stage C–H Functionalization
Chemical Reviews · 2023 · 10.1021/acs.chemrev.2c00478
Recent advances in the chemistry and applications of N-heterocyclic carbenes
Nature Reviews Chemistry · 2021 · 10.1038/s41570-021-00321-1
C–H Activation: Toward Sustainability and Applications
ACS Central Science · 2021 · 10.1021/acscentsci.0c01413
Triplet Energy Transfer Photocatalysis: Unlocking the Next Level
Chem · 2020 · 10.1016/j.chempr.2020.07.010
Energy transfer catalysis mediated by visible light: principles, applications, directions
Chemical Society Reviews · 2018 · 10.1039/c8cs00054a
Mild metal-catalyzed C–H activation: examples and concepts
Chemical Society Reviews · 2016 · https://doi.org/10.1039/c6cs00075d
Merging Visible Light Photoredox and Gold Catalysis
Accounts of Chemical Research · 2016 · 10.1021/acs.accounts.6b00351
Dual Catalysis Sees the Light: Combining Photoredox with Organo‐, Acid, and Transition‐Metal Catalysis
Chemistry - A European Journal · 2014 · 10.1002/chem.201304823
Formal SN‐Type Reactions in Rhodium(III)‐Catalyzed CH Bond Activation
Advanced Synthesis & Catalysis · 2014 · 10.1002/adsc.201400197
An overview of N-heterocyclic carbenes
Nature · 2014 · https://doi.org/10.1038/nature13384
Combining Gold and Photoredox Catalysis: Visible Light-Mediated Oxy- and Aminoarylation of Alkenes
Journal of the American Chemical Society · 2013 · 10.1021/ja400311h
C–H bond activation enables the rapid construction and late-stage diversification of functional molecules
Nature Chemistry · 2013 · https://doi.org/10.1038/nchem.1607
A robustness screen for the rapid assessment of chemical reactions
Nature Chemistry · 2013 · 10.1038/nchem.1669
Beyond Directing Groups: Transition‐Metal‐Catalyzed CH Activation of Simple Arenes
Angewandte Chemie International Edition · 2012 · https://doi.org/10.1002/anie.201203269
Organocatalytic umpolung: N-heterocyclic carbenes and beyond
Chemical Society Reviews · 2012 · 10.1039/c2cs15333e
Rh(III)-Catalyzed Directed C−H Olefination Using an Oxidizing Directing Group: Mild, Efficient, and Versatile
Journal of the American Chemical Society · 2011 · 10.1021/ja109676d
Extending NHC-Catalysis: Coupling Aldehydes with Unconventional Reaction Partners
Accounts of Chemical Research · 2011 · 10.1021/ar2000716
Towards mild metal-catalyzed C–H bond activation
Chemical Society Reviews · 2011 · https://doi.org/10.1039/c1cs15083a
Pyrrole Synthesis via Allylic sp3 C−H Activation of Enamines Followed by Intermolecular Coupling with Unactivated Alkynes
Journal of the American Chemical Society · 2010 · 10.1021/ja104305s
The Measure of All Rings—N‐Heterocyclic Carbenes
Angewandte Chemie International Edition · 2010 · 10.1002/anie.201001865
Surveying Sterically Demanding N-Heterocyclic Carbene Ligands with Restricted Flexibility for Palladium-catalyzed Cross-Coupling Reactions
Accounts of Chemical Research · 2008 · 10.1021/ar8000876
N-Heterocyclic Carbenes in Transition Metal Catalysis
Topics in organometallic chemistry · 2007 · 10.1007/978-3-540-36930-1
Asymmetric Heterogeneous Catalysis
Angewandte Chemie International Edition · 2006 · 10.1002/anie.200504212
Organocatalyzed Conjugate Umpolung of α,β‐Unsaturated Aldehydes for the Synthesis of γ‐Butyrolactones
Angewandte Chemie International Edition · 2004 · 10.1002/anie.200461572
Sterically Demanding, Bioxazoline-Derived N-Heterocyclic Carbene Ligands with Restricted Flexibility for Catalysis
Journal of the American Chemical Society · 2004 · 10.1021/ja045349r
Current projects
No projects listed.