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Cited by 802

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Selective oxidation of alcohols and aldehydes over supported metal nanoparticles

Davis, Sara E., Ide, Matthew S., Davis, Robert J.·2013·Green Chem.

Abstract

Oxidation is a key reaction in organic synthesis and will likely play a significant role in the development of value-added chemicals from biomass. The application of heterogeneous catalysis and molecular oxygen to oxidation reactions offers a green alternative to traditional, toxic chemical oxidants. However, making comparisons of catalyst performance (reaction rate, product selectivity) between reports in the literature is difficult because of inconsistencies in the ways results are reported. Herein, we examine the literature on supported metal catalysts for the oxidation of molecules of interest in biomass conversion (primary alcohols, polyols, 5-hydroxymethylfurfural, and various sugars). Reaction rates are calculated and compared in a consistent manner and recommendations for avoiding common pitfalls in kinetic investigations are made.

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Metadata

Authors
Davis, S. E., Ide, M. S., & Davis, R. J.
Venue
Green Chem.
Published
2013
Volume
15
Issue
1
Pages
17-45
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
OpenAlex
W2171599642
Cited by
802
References
1
FWCI
30.00
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Selective oxidation of alcohols and aldehydes over supported metal nanoparticles. https://app.cochat.ai/papers/10.1039/c2gc36441g
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Davis, S. E., Ide, M. S., & Davis, R. J. (2013). Selective oxidation of alcohols and aldehydes over supported metal nanoparticles. Green Chem. https://doi.org/10.1039/c2gc36441g

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.