Regioselective indium(III) trifluoromethanesulfonate-catalyzed hydrothiolation of non-activated olefins.
Identifieur interne : 002917 ( Main/Exploration ); précédent : 002916; suivant : 002918Regioselective indium(III) trifluoromethanesulfonate-catalyzed hydrothiolation of non-activated olefins.
Auteurs : RBID : pubmed:16391751English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Alkenes, Indium, Mesylates, Organometallic Compounds, Sulfhydryl Compounds.
- Catalysis, Cations, Cyclization, Models, Chemical, Molecular Structure.
Abstract
Indium(III) trifluoromethanesulfonate was found to be an excellent catalyst for the highly regioselective intra- and intermolecular addition of thiols to non-activated olefins and could be recycled and reused without loss of activity.
DOI: 10.1039/b513946e
PubMed: 16391751
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Weiwer, Michel" uniqKey="Weiwer M">Michel Weïwer</name>
<affiliation wicri:level="3"><nlm:affiliation>Laboratoire Arômes, Synthèses et Interactions, Université de Nice-Sophia Antipolis, Parc Valrose, 06108 Nice cedex 2, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire Arômes, Synthèses et Interactions, Université de Nice-Sophia Antipolis, Parc Valrose, 06108 Nice cedex 2</wicri:regionArea>
<placeName><region type="region" nuts="2">Provence-Alpes-Côte d'Azur</region>
<settlement type="city">Nice</settlement>
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<author><name sortKey="Coulombel, Lydie" uniqKey="Coulombel L">Lydie Coulombel</name>
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<author><name sortKey="Du Ach, Elisabet" uniqKey="Du Ach E">Elisabet Duñach</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkenes (chemistry)</term>
<term>Catalysis</term>
<term>Cations</term>
<term>Cyclization</term>
<term>Indium (chemistry)</term>
<term>Mesylates (chemistry)</term>
<term>Models, Chemical</term>
<term>Molecular Structure</term>
<term>Organometallic Compounds (chemistry)</term>
<term>Sulfhydryl Compounds (chemistry)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Alkenes</term>
<term>Indium</term>
<term>Mesylates</term>
<term>Organometallic Compounds</term>
<term>Sulfhydryl Compounds</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Catalysis</term>
<term>Cations</term>
<term>Cyclization</term>
<term>Models, Chemical</term>
<term>Molecular Structure</term>
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<front><div type="abstract" xml:lang="en">Indium(III) trifluoromethanesulfonate was found to be an excellent catalyst for the highly regioselective intra- and intermolecular addition of thiols to non-activated olefins and could be recycled and reused without loss of activity.</div>
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<DateRevised><Year>2013</Year>
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<Title>Chemical communications (Cambridge, England)</Title>
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<ArticleTitle>Regioselective indium(III) trifluoromethanesulfonate-catalyzed hydrothiolation of non-activated olefins.</ArticleTitle>
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<Abstract><AbstractText>Indium(III) trifluoromethanesulfonate was found to be an excellent catalyst for the highly regioselective intra- and intermolecular addition of thiols to non-activated olefins and could be recycled and reused without loss of activity.</AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Weïwer</LastName>
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