Helena Lundberg
Papers
1
Total Citations
31
H-Index
1
About
Helena Lundberg is a leading figure in the field of asymmetric catalysis and synthetic methodology, with a particular focus on the development of sustainable and efficient catalytic systems for organic transformations. Her work has made significant contributions to the design and high-throughput screening of novel catalyst libraries, notably for the asymmetric transfer hydrogenation of heteroaromatic ketones. This research is exemplified by her highly cited 2012 study, which has garnered 31 citations, where she demonstrated the use of amino acid-based ligands—including hydroxy amide, thioamide, and hydroxamic acid functionalities—combined with ruthenium and rhodium complexes. A landmark achievement of this work was the application of these catalysts in the formal syntheses of the pharmaceuticals (R)-Fluoxetine and (S)-Duloxetine, showcasing the practical utility of her methodology for producing enantiomerically pure compounds. Through her innovative approach to catalyst discovery and reaction optimization, Lundberg has advanced the field of green chemistry by enabling more selective and less wasteful synthetic routes, establishing her as a key contributor to modern asymmetric synthesis.
Research Focus
Key Achievements
Top Papers
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