Nature Catalysis

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Nature Catalysis publishes high quality work across all areas of catalysis, including both fundamental and applied studies. https://www.nature.com/natcatal/

New online! Chiral phosphorus by catalyst design: Nature Catalysis, Published online: 05 August 2026; doi:10.1038/s41929-026-01594-9Phosphorothioate modifications are central to oligonucleotide medicines, but their stereocontrolled syntheses has proven challenging. A catalyst-controlled loading…

Chiral phosphorus by catalyst design

Nature Catalysis, Published online: 05 August 2026; doi:10.1038/s41929-026-01594-9Phosphorothioate modifications are central to oligonucleotide medicines, but their stereocontrolled syntheses has proven challenging. A catalyst-controlled loading strategy now delivers stereodefined building blocks for oligonucleotides and cyclic dinucleotides.

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New online! Uncovering the source of uncertainty: Nature Catalysis, Published online: 31 July 2026; doi:10.1038/s41929-026-01572-1Constructing reliable models for the discovery of heterogeneous catalysts requires high-quality data. This round-robin study reveals the need for rigorous assessment of…

Uncovering the source of uncertainty

Nature Catalysis, Published online: 31 July 2026; doi:10.1038/s41929-026-01572-1Constructing reliable models for the discovery of heterogeneous catalysts requires high-quality data. This round-robin study reveals the need for rigorous assessment of uncertainty when selecting the input and output features of data-driven models.

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New online! Unlocking ketene–Heck coupling via activation energy modulation in Pd catalysis: Nature Catalysis, Published online: 13 July 2026; doi:10.1038/s41929-026-01579-8The Heck reaction is one of the most widely utilized in organic chemistry. Now the authors present a Heck-type transformation…

Unlocking ketene–Heck coupling via activation energy modulation in Pd catalysis

Nature Catalysis, Published online: 13 July 2026; doi:10.1038/s41929-026-01579-8The Heck reaction is one of the most widely utilized in organic chemistry. Now the authors present a Heck-type transformation for the direct conversion of saturated acid chlorides into α,β-unsaturated ketones with iodoarenes via ketenes.

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