Journal article Closed Access
Helbing, Tim;
Georg, Mats;
Stöhr, Fabian;
Carraro, Caterina;
Becker, Jonathan;
Gatto, Barbara;
Göttlich, Richard
{ "@context": "https://schema.org/", "@id": "https://doi.org/10.1002/ejoc.202101072", "@type": "ScholarlyArticle", "creator": [ { "@id": "https://orcid.org/0000-0002-1284-3254", "@type": "Person", "affiliation": "Institute of Organic Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany", "name": "Helbing, Tim" }, { "@type": "Person", "affiliation": "Institute of Organic Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany", "name": "Georg, Mats" }, { "@type": "Person", "affiliation": "Institute of Organic Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany; Institute of Inorganic and Analytical Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany", "name": "St\u00f6hr, Fabian" }, { "@type": "Person", "affiliation": "Department of Pharmaceutical and Pharmacological Sciences University of Padova Via Francesco Marzolo 5 35131 Padova Italy", "name": "Carraro, Caterina" }, { "@id": "https://orcid.org/0000-0002-6708-8604", "@type": "Person", "affiliation": "Institute of Inorganic and Analytical Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany", "name": "Becker, Jonathan" }, { "@id": "https://orcid.org/0000-0001-9465-6913", "@type": "Person", "affiliation": "Department of Pharmaceutical and Pharmacological Sciences University of Padova Via Francesco Marzolo 5 35131 Padova Italy", "name": "Gatto, Barbara" }, { "@id": "https://orcid.org/0000-0002-1424-3084", "@type": "Person", "affiliation": "Institute of Organic Chemistry Justus Liebig University Giessen Heinrich-Buff-Ring 17 35392 Giessen Germany", "name": "G\u00f6ttlich, Richard" } ], "datePublished": "2021-09-29", "description": "AbstractThe present study describes the kinetic analysis of the 3\u2010chloropiperidine alkylation mechanism. These nitrogen mustard\u2010based compounds are expected to react via a highly electrophilic bicyclic aziridinium ion, which is readily attacked by nucleophiles. Halide abstraction using silver salts with weakly coordinating anions lead to the isolation of these proposed intermediates, whereas their structure was confirmed by single crystal XRD. Kinetic studies of the aziridinium ions also revealed notable reactivity differences of the C5 gem\u2010methylated compounds and their unmethylated counterparts. The observed reactivity trends were also reflected by NMR studies in aqueous solution and DNA alkylation experiments of the related 3\u2010chloropiperidines. Therefore, the underlying Thorpe\u2010Ingold effect might be considered as another option to adjust the alkylation activity of these compounds.", "headline": "Understanding the Alkylation Mechanism of 3\u2010Chloropiperidines \u2013 NMR Kinetic Studies and Isolation of Bicyclic Aziridinium Ions", "identifier": "https://doi.org/10.1002/ejoc.202101072", "image": "https://zenodo.org/static/img/logos/zenodo-gradient-round.svg", "inLanguage": { "@type": "Language", "alternateName": "eng", "name": "English" }, "keywords": [ "Organic Chemistry", "Physical and Theoretical Chemistry" ], "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Understanding the Alkylation Mechanism of 3\u2010Chloropiperidines \u2013 NMR Kinetic Studies and Isolation of Bicyclic Aziridinium Ions", "url": "https://www.openaccessrepository.it/record/207882" }
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