Ionic Liquids as Designer Solvents for Nucleophilic Aromatic Substitutions

Ionic liquids were designed to optimize the nucleophilic aromatic substitution reaction of an activated aniline with an activated arylhalide. The design was achieved by selecting the anions on the basis of calculations of the gas-phase basicity of their conjugate acids.

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PID https://www.doi.org/10.1021/ol702435f
PID https://www.doi.org/10.1021/ol702435f.s003
URL https://pubs.acs.org/doi/pdf/10.1021/ol702435f
URL https://pubs.acs.org/doi/10.1021/ol702435f
URL http://www.ncbi.nlm.nih.gov/pubmed/18001045
URL https://figshare.com/articles/journal_contribution/Ionic_Liquids_as_Designer_Solvents_for_Nucleophilic_Aromatic_Substitutions/2970529
URL http://dx.doi.org/10.1021/ol702435f
URL https://academic.microsoft.com/#/detail/2012429772
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Access Right Open Access
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Author Tom Welton, 0000-0002-1750-1683
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Collected From ORCID; Datacite; figshare; Crossref; Microsoft Academic Graph
Hosted By Organic Letters; figshare
Publication Date 2007-12-01
Publisher American Chemical Society (ACS)
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Language UNKNOWN
Resource Type Other literature type; Article
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Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::d04b599995f93ddb5d8e6eb7e061fadf
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Last Updated 24 December 2020, 14:44 (CET)
Created 24 December 2020, 14:44 (CET)