Peter R. Schreiner, Justus Liebig University Giessen, discusses his research, interdisciplinary education, chemistry's role in fostering collaboration and critical thinking, leadership in the GDCh, and his passion for music

Thinking About Organic Chemistry Through the Lens of Underlying Physics

C-Scorpionate Complexes Catalyze Nitroarene Reduction for the First Time
Luísa Martins, Portugal, discusses a recently published study exploring the effects of catalysts, solvents, and reducing agents on the reaction kinetics of nitroarene reduction
![Synthesis of [c2]Daisy Chains via Mechanochemistry](https://www.chemistryviews.org/wp-content/uploads/2025/04/202504_RotaxanesWithSolidStateMechanochemistry-125x94.png)
Synthesis of [c2]Daisy Chains via Mechanochemistry
Solid-state mechanochemistry enables the synthesis of stoppered [c2]daisy chains from pillar[5]arene derivatives without solvents

Green Allylation of Carbohydrates: A Tin-Free Route to Industrial Sorbitol Derivatives
An eco-friendly allylation of unprotected carbohydrates in water, eliminating toxic tin reagents

Most Accessed Articles: March 2025
Highlights from Chemistry Europe, ACES, and GDCh journals

Angewandte Chemie 15/2025: Exciting Ambience
Overview of the latest issue of Angewandte Chemie

Light-Activated Catalyst Resets Carbon–Halogen Bonds to Turn Racemates into Enantiomer-Enriched Products
A new light-activated catalyst enables deracemization via carbon–halogen bond cleavage—the first of its kind targeting heteroatom bonds—offering a streamlined route to chiral pharmaceuticals

Unorthodox Catalysts for Diels-Alder Reactions
E. H. Tiekink, R. Verdijk, T. A. Hamlin, F. M. Bickelhaupt used quantum chemistry to show that hydrogen-bonding organocatalysts speed up the Diels–Alder reaction

Believing in the Power of Collaboration
Dr. Tim Kinzel, Executive Director of the GDCh, speaks here about the importance of volunteer engagement, collaboration, and addressing the changing needs of society as a central task of modern chemical societies

Method Simplifies Deprotection and Modification of N-Heterocycles
A mild, efficient system for selectively deprotecting and modifying N-heterocycles in a single step