Indium-promoted Reformatsky reaction: a straightforward access to β-amino and β-hydroxy α,α-difluoro carbonyl compounds.
Identifieur interne : 000C66 ( Main/Exploration ); précédent : 000C65; suivant : 000C67Indium-promoted Reformatsky reaction: a straightforward access to β-amino and β-hydroxy α,α-difluoro carbonyl compounds.
Auteurs : RBID : pubmed:22998653English descriptors
- KwdEn :
- MESH :
- chemical , chemical synthesis : Hydrocarbons, Fluorinated.
- chemical , chemistry : Aldehydes, Hydrocarbons, Fluorinated, Imines, Indium, Ketones.
- Molecular Structure.
Abstract
A versatile and practical methodology to access β-amino and β-hydroxy α,α-difluoro carbonyl compounds using indium metal is described. This methodology has been successfully applied to a broad range of substrates including aldehydes, ketones, and imines, affording the corresponding and highly valuable gem-difluoro esters. The wide substrate scope highlights the chemoselectivity of the process.
DOI: 10.1021/jo301873y
PubMed: 22998653
Links toward previous steps (curation, corpus...)
Le document en format XML
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<author><name sortKey="Poisson, Thomas" uniqKey="Poisson T">Thomas Poisson</name>
<affiliation wicri:level="3"><nlm:affiliation>INSA de Rouen, Avenue de l'Université, 76800 St Etienne du Rouvray, France. thomas.poisson@insa-rouen.fr</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>INSA de Rouen, Avenue de l'Université, 76800 St Etienne du Rouvray</wicri:regionArea>
<placeName><region type="region" nuts="2">Haute-Normandie</region>
<settlement type="city">St Etienne du Rouvray</settlement>
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<author><name sortKey="Belhomme, Marie Charlotte" uniqKey="Belhomme M">Marie-Charlotte Belhomme</name>
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<author><name sortKey="Pannecoucke, Xavier" uniqKey="Pannecoucke X">Xavier Pannecoucke</name>
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<term>Hydrocarbons, Fluorinated (chemical synthesis)</term>
<term>Hydrocarbons, Fluorinated (chemistry)</term>
<term>Imines (chemistry)</term>
<term>Indium (chemistry)</term>
<term>Ketones (chemistry)</term>
<term>Molecular Structure</term>
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<term>Imines</term>
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<front><div type="abstract" xml:lang="en">A versatile and practical methodology to access β-amino and β-hydroxy α,α-difluoro carbonyl compounds using indium metal is described. This methodology has been successfully applied to a broad range of substrates including aldehydes, ketones, and imines, affording the corresponding and highly valuable gem-difluoro esters. The wide substrate scope highlights the chemoselectivity of the process.</div>
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<Title>The Journal of organic chemistry</Title>
<ISOAbbreviation>J. Org. Chem.</ISOAbbreviation>
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<Abstract><AbstractText>A versatile and practical methodology to access β-amino and β-hydroxy α,α-difluoro carbonyl compounds using indium metal is described. This methodology has been successfully applied to a broad range of substrates including aldehydes, ketones, and imines, affording the corresponding and highly valuable gem-difluoro esters. The wide substrate scope highlights the chemoselectivity of the process.</AbstractText>
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