Chemists at the Max-Planck-Institut für Kohlenforschung have developed a practical two-step method for alkylating alkenes via ...
A line structure of a molecule derived from the natural product 3-carene; the parent 3-carene structure, featuring a ...
The novel method uses a recycling photoreactor with an immobilized photosensitizer, coupled with a high-performance liquid chromatography technology, to enable efficient and sustainable synthesis of Z ...
Chemists at the Max-Planck-Institut für Kohlenforschung have solved a decades-old synthetic puzzle, developing a practical, two-step method for the alkylation of alkenes via thianthrenation. The ...
This study is led by Prof. Dr. Shengying Li (State Key Laboratory of Microbial Technology, Shandong University) and Ass. Prof. Dr. Biaobiao Zhang (School of Science, Westlake University). The team ...
Researchers have discovered a new way to drive chemical reactions that could generate a wide variety of azetidines -- four-membered nitrogen heterocycles that have desirable pharmaceutical properties.
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A drug discovery bottleneck? How cheaper reagents could speed branched molecule synthesis
When chemists design drug candidates, shape matters enormously. Many active pharmaceutical ingredients contain branched carbon structures—points where the molecular chain forks in a specific direction ...
Azetidines, four-sided rings made of three carbon atoms and a nitrogen, are a handy molecular motif in applications as diverse as drug design and rocket fuels. The most efficient way to assemble them ...
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