Cited by 43Physical Organic Chemistry and Reaction KineticsCoordination Chemistry and OrganometallicsOxidative Organic Chemistry Reactions

A study of superoxide reactivity. Reaction of potassium superoxide with alkyl halides and tosylates

Chern, Chuen-Ing, DiCosimo, Robert, De Jesus, Reynalda, San Filippo, Joseph·1978·Journal of the American Chemical Society

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTA study of superoxide reactivity. Reaction of potassium superoxide with alkyl halides and tosylatesChuen-Ing Chern, Robert DiCosimo, Reynalda De Jesus, and Joseph San Filippo Jr.Cite this: J. Am. Chem. Soc. 1978, 100, 23, 7317–7327Publication Date (Print):November 1, 1978Publication History Published online1 May 2002Published inissue 1 November 1978https://pubs.acs.org/doi/10.1021/ja00491a032https://doi.org/10.1021/ja00491a032research-articleACS PublicationsRequest reuse permissionsArticle Views424Altmetric-Citations32LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts

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  • Na2O has been found to be less reactive than K2O due to its reduced solubility.

    “Na2O has been found to be less reactive than K2O due to its reduced solubility [56].”
  • O2•− is a nucleophile in reactions with alkyl halides and alkyl tosylates in DMSO, leading to alkylperoxy radicals and then peroxy anions via one-electron reduction.

    “O2•− is a nucleophile in the reaction with alkyl halides and alkyl tosylates in DMSO and leads to the formation of alkylperoxy radicals and subsequently to peroxy anions via one-electron reduction [56,129], Figure 47.”

Cited by

Sorted by citations

Authors
Chern, C.-I., DiCosimo, R., De Jesus, R., & San Filippo, J.
Venue
Journal of the American Chemical Society
Published
1978-11
Volume
100
Issue
23
Pages
7317-7327
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2953227684
Cited by
43
References
0
Citations by year
2025: 2 · 2024: 1 · 2023: 1 · 2021: 1 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 2
FWCI
4.70
Type
journal article
Language
en
Open access
closed
Locations
Journal of the American Chemical Society (publishedVersion)
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Physical Organic Chemistry and Reaction Kinetics
  • Physical Sciences › Chemistry › Organic Chemistry › Coordination Chemistry and Organometallics
  • Physical Sciences › Chemistry › Organic Chemistry › Oxidative Organic Chemistry Reactions
Keywords
potassium superoxide, alkyl halides, tosylate, alkyl radicals

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