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Earth-abundant iron catalysis enables access to valuable dialkylated compounds

Earth-abundant iron catalysis enables access to valuable dialkylated compounds
Schematic showing the design of a new iron-catalyzed dialkylation reaction that transforms abundant alkenes to prized C(sp3)-rich molecules. Credit: Nature Catalysis (2024). DOI: 10.1038/s41929-024-01113-8

National University of Singapore (NUS) chemists have solved a longstanding challenge in the synthesis of congested C(sp3)-rich molecules by developing a new iron-catalyzed reaction that generates two alkyl-alkyl bonds in crowded environments. The work is published in Nature Catalysis.

C(sp3)–C(sp3) bonds are single, strong bonds formed between two . They form the backbones of many biologically active natural products and synthetic .

Research has shown that the number of saturated (sp3) carbons correlates with solubility, suggesting that increased saturation leads to enhanced potency and selectivity in drugs. However, developing methods to construct C(sp3)-rich scaffolds is an important but challenging goal in . This is because reactions involving sp3-hybridized substrates are typically inefficient and prone to undesired product formation.

A research team led by Associate Professor Koh Ming Joo, from the Department of Chemistry, NUS have conceived a new strategy that harnesses an earth-abundant (terpyridine) iron catalyst to combine alkenes with sp3-hybridized organohalides and organozinc reagents.

This approach allows them to add different-sized alkyl groups to the alkene, resulting in a library of drug-like molecules with congested cores containing either carbon- or heteroatom-substituted stereocenters. The method is useful for creating valuable but challenging C(sp3)-rich molecules.

This research is a collaboration with Dr. Xinglong Zhang from the Institute of High Performance Computing, Agency for Science, Technology and Research (ASTAR) and Professor Patrick Holland from Yale University.

Prof Koh said, "Our studies suggest that this iron-catalyzed dialkylation reaction operates through a unique mechanism, which potentially opens the door to a wider range of transformations and new chemical space. This helps to diversify and broaden the chemical structures of performance molecules."

"We believe this method will accelerate the synthesis of many natural products and pharmaceuticals in a sustainable manner, especially those that contain densely functionalized alkyl-alkyl linkages," added Prof Koh.

The research team is leveraging the newly discovered iron-catalyzed system to transform other classes of organic starting materials into useful compounds for various applications, including drug development.

More information: Tong-De Tan et al, Congested C(sp3)-rich architectures enabled by iron-catalysed conjunctive alkylation, Nature Catalysis (2024). DOI: 10.1038/s41929-024-01113-8

Journal information: Nature Catalysis

Citation: Earth-abundant iron catalysis enables access to valuable dialkylated compounds (2024, March 6) retrieved 27 April 2024 from https://phys.org/news/2024-03-earth-abundant-iron-catalysis-enables.html
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