Default: Nature Chemistry

ISSN: 1755-4330

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Nature Chemistry Q1 Unclaimed

Nature Publishing Group United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Nature Chemistry is a journal indexed in SJR in Chemical Engineering (miscellaneous) and Chemistry (miscellaneous) with an H index of 232. It has an SJR impact factor of 9,996 and it has a best quartile of Q1. It has an SJR impact factor of 9,996.

Nature Chemistry focuses its scope in these topics and keywords: allylic, asymmetric, chirality, selective, arylation, synthesis, palladiumcatalysed, chiral, chemoenzymatic, chemo, ...

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Metrics

Nature Chemistry

9,996

SJR Impact factor

232

H Index

203

Total Docs (Last Year)

635

Total Docs (3 years)

7471

Total Refs

9958

Total Cites (3 years)

525

Citable Docs (3 years)

15,26

Cites/Doc (2 years)

36,80

Ref/Doc

Aims and Scope


allylic, asymmetric, chirality, selective, arylation, synthesis, palladiumcatalysed, chiral, chemoenzymatic, chemo, chemistrystreamlining, decarboxylative, complexesentropic, construction, contribute, correlations, crystalsorganocatalytic, d, catalysismaterials, capsules, activity, alcoholsbarium, alkanesfrantically, alkylation, aminated, approach, aromatic, aromaticityinterfacial, arylboronic, azaallyls, azo, behaviourpredicting, bright,


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A chemist's cup of tea

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A chiral catalyst with a ring to it

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A display of sensitivity

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A metal-free landmark

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A new twist

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A photoswitchable polar crystal that exhibits superionic conduction

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A stable heavier group 14 analogue of vinylidene

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A total-synthesis framework for the construction of high-order colloidal hybrid nanoparticles

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At a stretch

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Catalysis in a drought

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Catalytic transport of molecular cargo using diffusive binding along a polymer track

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Caught in a trap

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Cerium under the lens

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Chiral-auxiliary-mediated 1,2-cis-glycosylations for the solid-supported synthesis of a biologically important branched a-glucan

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Chirality transfer takes a jump

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Component-based syntheses of trioxacarcin A, DC-45-A1 and structural analogues

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Conformer-specific hydrogen atom tunnelling in trifluoromethylhydroxycarbene

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Control and imaging of O(1D2) precession

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Coupling clusters

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Demystifying the asymmetry-amplifying, autocatalytic behaviour of the Soai reaction through structural, mechanistic and computational studies

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Detection by failure

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Diverse sp3 C-H functionalization through alcohol beta-sulfonyloxylation

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