Silvia Elfert

Deconstructing Covalent Organocatalysis

X‐ray Crystallography in Open‐Framework Materials

Organocatalytic umpolung: N-heterocyclic carbenes and beyond

An overview of N-heterocyclic carbenes

Functional diversity of organic molecule enzyme cofactors

Mapping‐Out Catalytic Processes in a Metal–Organic Framework with Single‐Crystal X‐ray Crystallography

Mapping‐Out Catalytic Processes in a Metal–Organic Framework with Single‐Crystal X‐ray Crystallography

The Hitchhiker’s Guide to Flow Chemistry

Unveiling the Delicate Balance of Steric and Dispersion Interactions in Organocatalysis Using High-Level Computational Methods

The effect of the N-mesityl group in NHC-catalyzed reactions

Multicomponent reactions: advanced tools for sustainable organic synthesis

Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

Röntgenkristallographie an Materialien mit offenen Gerüsten

Chemomimetic Biocatalysis: Exploiting the Synthetic Potential of Cofactor-Dependent Enzymes To Create New Catalysts

Evolution of asymmetric organocatalysis: multi- and retrocatalysis

Mechanistic Investigation of the Enantioselective Intramolecular Stetter Reaction: Proton Transfer Is the First Irreversible Step

Aldehyde Umpolung by N‐Heterocyclic Carbenes: NMR Characterization of the Breslow Intermediate in its Keto Form, and a Spiro‐Dioxolane as the Resting State of the Catalytic System

Characterization of the Key Intermediates of Carbene‐Catalyzed Umpolung by NMR Spectroscopy and X‐Ray Diffraction: Breslow Intermediates, Homoenolates, and Azolium Enolates

Umpolung by N‐Heterocyclic Carbenes: Generation and Reactivity of the Elusive 2,2‐Diamino Enols (Breslow Intermediates)

Charakterisierung der Schlüsselintermediate von carbenkatalysierten Umpolungen durch Kristallstrukturanalyse/NMR‐Spektroskopie: Breslow‐Intermediate, Homoenolate und Azoliumenolate

Umpolung mit N‐heterocyclischen Carbenen: Generierung und Reaktivität von Breslow‐Intermediaten (2,2‐Diaminoenole)

Umpolung von Aldehyden mit N‐heterocyclischen Carbenen: NMR‐Charakterisierung des Breslow‐Intermediats in seiner Ketoform und eines Spirodioxolans als “resting state” des katalytischen Systems