Nature Catalysis
Overview
Nature Catalysis is a prestigious scientific journal that publishes cutting-edge research in the field of catalysis. It covers a wide range of topics, including heterogeneous, homogeneous, and enzymatic catalysis, with a focus on fundamental understanding, design, and application of catalysts. The journal showcases groundbreaking studies that contribute to the development of sustainable and efficient chemical processes, making it an essential resource for researchers and professionals in the field.
Details
Details
Metrics
Metrics
h-index / Ranks: 1746
136
SJR / Ranks: 42
13315
CiteScore / Ranks: 50
53.00
JIF / Ranks: 52
37.8
Recent Articles
1.
Dooley C, Ibba F, Botlik B, Palladino C, Goult C, Gao Y, et al.
Nat Catal
. 2025 Feb;
8(2):107-115.
PMID: 40017632
Catalytic enantioconvergent nucleophilic substitution reactions of alkyl halides are highly valuable transformations, but they are notoriously difficult to implement. Specifically, nucleophilic fluorination is a renowned challenge, especially when inexpensive alkali...
2.
Solomon J, Lee C, Liu Y, Duffin C, Ribbe M, Hu Y
Nat Catal
. 2024 Dec;
7(10):1130-1141.
PMID: 39713742
Heterologous expression of nitrogenase has been actively pursued because of the far-reaching impact of this enzyme on agriculture, energy and environment. Yet, isolation of an active two-component, metallocentre-containing nitrogenase from...
3.
Little R, Paiva F, Jenkins R, Hong H, Sun Y, Demydchuk Y, et al.
Nat Catal
. 2024 Dec;
2(11):1045-1054.
PMID: 39659772
Enzymes catalysing remarkable Diels-Alder-like [4+2] cyclisations have been previously implicated in the biosynthesis of spirotetronate and spirotetramate antibiotics. Biosynthesis of the polyether antibiotic tetronasin is not anticipated to require such...
4.
Yu C, Zhang Z, Dong G
Nat Catal
. 2024 Nov;
7(4):432-440.
PMID: 39555146
Constructive functionalization of unstrained aryl-aryl bonds has been a fundamental challenge in organic synthesis due to the inertness of these bonds. Here we report a split cross-coupling strategy that allows...
5.
Day C, Renteria-Gomez A, Ton S, Gogoi A, Gutierrez O, Martin R
Nat Catal
. 2024 Nov;
6(3):244-253.
PMID: 39525327
Polypyridine-ligated nickel complexes are widely used as privileged catalysts in a variety of cross-coupling reactions. The rapid adoption of these complexes is tentatively attributed to their ability to shuttle between...
6.
Guan X, Xie Y, Liu C
Nat Catal
. 2024 Nov;
7(5):475-482.
PMID: 39524322
Hybrid systems that integrate synthetic materials with biological machinery offer opportunities for sustainable and efficient catalysis. However, the multidisciplinary and unique nature of the materials-biology interface requires researchers to draw...
7.
Wu F, Chintawar C, Lalisse R, Mukherjee P, Dutta S, Tyler J, et al.
Nat Catal
. 2024 Nov;
7(3):242-251.
PMID: 39512751
Skeletal editing has received unprecedented attention as an emerging technology for the late-stage manipulation of molecular scaffolds. The direct achievement of functionalized carbon-atom insertion in aromatic rings is challenging. Despite...
8.
Choudhury S, Narayanan B, Moret M, Hatzimanikatis V, Miskovic L
Nat Catal
. 2024 Oct;
7(10):1086-1098.
PMID: 39463726
Generating large omics datasets has become routine for gaining insights into cellular processes, yet deciphering these datasets to determine metabolic states remains challenging. Kinetic models can help integrate omics data...
9.
Mao R, Gao S, Qin Z, Rogge T, Wu S, Li Z, et al.
Nat Catal
. 2024 Jul;
7(5):585-592.
PMID: 39006156
Intermolecular functionalization of tertiary C-H bonds to construct fully substituted stereogenic carbon centers represents a formidable challenge: without the assistance of directing groups, state-of-the-art catalysts struggle to introduce chirality to...
10.
Hu X, Cheng-Sanchez I, Kong W, Molander G, Nevado C
Nat Catal
. 2024 Jul;
7(6):655-665.
PMID: 38947227
The development of novel strategies to rapidly construct complex chiral molecules from readily available feedstocks is a long-term pursuit in the chemistry community. Radical-mediated alkene difunctionalizations represent an excellent platform...