Serveur d'exploration sur le LRGP

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies

Identifieur interne : 001308 ( Istex/Corpus ); précédent : 001307; suivant : 001309

A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies

Auteurs : Baptiste Manteau ; Pierre Genix ; Lydia Brelot ; Jean-Pierre Vors ; Sergiy Pazenok ; Florence Giornal ; Charlotte Leuenberger ; Frédéric R. Leroux

Source :

RBID : ISTEX:A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5

English descriptors

Abstract

The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.

Url:
DOI: 10.1002/ejoc.201000958

Links to Exploration step

ISTEX:A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5

Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
<author>
<name sortKey="Manteau, Baptiste" sort="Manteau, Baptiste" uniqKey="Manteau B" first="Baptiste" last="Manteau">Baptiste Manteau</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Genix, Pierre" sort="Genix, Pierre" uniqKey="Genix P" first="Pierre" last="Genix">Pierre Genix</name>
<affiliation>
<mods:affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Brelot, Lydia" sort="Brelot, Lydia" uniqKey="Brelot L" first="Lydia" last="Brelot">Lydia Brelot</name>
<affiliation>
<mods:affiliation>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Vors, Jean Ierre" sort="Vors, Jean Ierre" uniqKey="Vors J" first="Jean-Pierre" last="Vors">Jean-Pierre Vors</name>
<affiliation>
<mods:affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Pazenok, Sergiy" sort="Pazenok, Sergiy" uniqKey="Pazenok S" first="Sergiy" last="Pazenok">Sergiy Pazenok</name>
<affiliation>
<mods:affiliation>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Giornal, Florence" sort="Giornal, Florence" uniqKey="Giornal F" first="Florence" last="Giornal">Florence Giornal</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Leuenberger, Charlotte" sort="Leuenberger, Charlotte" uniqKey="Leuenberger C" first="Charlotte" last="Leuenberger">Charlotte Leuenberger</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Leroux, Frederic R" sort="Leroux, Frederic R" uniqKey="Leroux F" first="Frédéric R." last="Leroux">Frédéric R. Leroux</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5</idno>
<date when="2010" year="2010">2010</date>
<idno type="doi">10.1002/ejoc.201000958</idno>
<idno type="url">https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001308</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001308</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
<author>
<name sortKey="Manteau, Baptiste" sort="Manteau, Baptiste" uniqKey="Manteau B" first="Baptiste" last="Manteau">Baptiste Manteau</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Genix, Pierre" sort="Genix, Pierre" uniqKey="Genix P" first="Pierre" last="Genix">Pierre Genix</name>
<affiliation>
<mods:affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Brelot, Lydia" sort="Brelot, Lydia" uniqKey="Brelot L" first="Lydia" last="Brelot">Lydia Brelot</name>
<affiliation>
<mods:affiliation>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Vors, Jean Ierre" sort="Vors, Jean Ierre" uniqKey="Vors J" first="Jean-Pierre" last="Vors">Jean-Pierre Vors</name>
<affiliation>
<mods:affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Pazenok, Sergiy" sort="Pazenok, Sergiy" uniqKey="Pazenok S" first="Sergiy" last="Pazenok">Sergiy Pazenok</name>
<affiliation>
<mods:affiliation>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Giornal, Florence" sort="Giornal, Florence" uniqKey="Giornal F" first="Florence" last="Giornal">Florence Giornal</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Leuenberger, Charlotte" sort="Leuenberger, Charlotte" uniqKey="Leuenberger C" first="Charlotte" last="Leuenberger">Charlotte Leuenberger</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Leroux, Frederic R" sort="Leroux, Frederic R" uniqKey="Leroux F" first="Frédéric R." last="Leroux">Frédéric R. Leroux</name>
<affiliation>
<mods:affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</mods:affiliation>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j" type="main">European Journal of Organic Chemistry</title>
<title level="j" type="alt">EUROPEAN JOURNAL OF ORGANIC CHEMISTRY</title>
<idno type="ISSN">1434-193X</idno>
<idno type="eISSN">1099-0690</idno>
<imprint>
<biblScope unit="vol">2010</biblScope>
<biblScope unit="issue">31</biblScope>
<biblScope unit="page" from="6043">6043</biblScope>
<biblScope unit="page" to="6066">6066</biblScope>
<biblScope unit="page-count">24</biblScope>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="2010-11">2010-11</date>
</imprint>
<idno type="ISSN">1434-193X</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">1434-193X</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Ammonium</term>
<term>Ammonium formate</term>
<term>Aqueous layer</term>
<term>Aqueous sodium hydrogen carbonate</term>
<term>Aqueous sodium hydroxide</term>
<term>Aqueous solution</term>
<term>Azide</term>
<term>Benzenesulfonyl</term>
<term>Benzenesulfonyl azide</term>
<term>Butyllithium</term>
<term>Calcd</term>
<term>Carbonate</term>
<term>Carboxylation</term>
<term>Cd3od</term>
<term>Cdcl3</term>
<term>Chem</term>
<term>Chloroform</term>
<term>Citric acid</term>
<term>Colorless</term>
<term>Colorless needles</term>
<term>Colorless powder</term>
<term>Cooh</term>
<term>Crude product</term>
<term>Cyclohexane</term>
<term>Dichloromethane</term>
<term>Diethyl</term>
<term>Diethyl ether</term>
<term>Dihedral angle</term>
<term>Diisopropylamine</term>
<term>Dropwise</term>
<term>Dropwise addition</term>
<term>Eluent</term>
<term>Equiv</term>
<term>Ether</term>
<term>Ethyl</term>
<term>Ethyl acetate</term>
<term>Excess chlorine</term>
<term>Filtrate</term>
<term>Fluorine chem</term>
<term>Formate</term>
<term>Full paper</term>
<term>Gmbh</term>
<term>Hexane</term>
<term>Hrms</term>
<term>Hydrochloric</term>
<term>Hydrochloric acid</term>
<term>Hydroxide</term>
<term>Kgaa</term>
<term>Leroux</term>
<term>Mbar</term>
<term>Methanol</term>
<term>Methoxy</term>
<term>Methoxy group</term>
<term>Mmol</term>
<term>Occl3</term>
<term>Ocf2cl</term>
<term>Ocf2cl byproduct</term>
<term>Ocf3</term>
<term>Ocf3 group</term>
<term>Organic layers</term>
<term>Propionitrile</term>
<term>Pure acid</term>
<term>Pure product</term>
<term>Pyridine</term>
<term>Pyridine ring</term>
<term>Reaction mixture</term>
<term>Reflux</term>
<term>Sbcl5</term>
<term>Sbf3</term>
<term>Schlosser</term>
<term>Sodium hydroxide</term>
<term>Sodium sulfate</term>
<term>Sulfate</term>
<term>Tetrabutylammonium fluoride</term>
<term>Thiophosgene</term>
<term>Toluene</term>
<term>Trifluoromethoxy</term>
<term>Verlag</term>
<term>Verlag gmbh</term>
<term>Weinheim</term>
<term>White powder</term>
<term>Yellow solution</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en">
<term>Ammonium</term>
<term>Ammonium formate</term>
<term>Aqueous layer</term>
<term>Aqueous sodium hydrogen carbonate</term>
<term>Aqueous sodium hydroxide</term>
<term>Aqueous solution</term>
<term>Azide</term>
<term>Benzenesulfonyl</term>
<term>Benzenesulfonyl azide</term>
<term>Butyllithium</term>
<term>Calcd</term>
<term>Carbonate</term>
<term>Carboxylation</term>
<term>Cd3od</term>
<term>Cdcl3</term>
<term>Chem</term>
<term>Chloroform</term>
<term>Citric acid</term>
<term>Colorless</term>
<term>Colorless needles</term>
<term>Colorless powder</term>
<term>Cooh</term>
<term>Crude product</term>
<term>Cyclohexane</term>
<term>Dichloromethane</term>
<term>Diethyl</term>
<term>Diethyl ether</term>
<term>Dihedral angle</term>
<term>Diisopropylamine</term>
<term>Dropwise</term>
<term>Dropwise addition</term>
<term>Eluent</term>
<term>Equiv</term>
<term>Ether</term>
<term>Ethyl</term>
<term>Ethyl acetate</term>
<term>Excess chlorine</term>
<term>Filtrate</term>
<term>Fluorine chem</term>
<term>Formate</term>
<term>Full paper</term>
<term>Gmbh</term>
<term>Hexane</term>
<term>Hrms</term>
<term>Hydrochloric</term>
<term>Hydrochloric acid</term>
<term>Hydroxide</term>
<term>Kgaa</term>
<term>Leroux</term>
<term>Mbar</term>
<term>Methanol</term>
<term>Methoxy</term>
<term>Methoxy group</term>
<term>Mmol</term>
<term>Occl3</term>
<term>Ocf2cl</term>
<term>Ocf2cl byproduct</term>
<term>Ocf3</term>
<term>Ocf3 group</term>
<term>Organic layers</term>
<term>Propionitrile</term>
<term>Pure acid</term>
<term>Pure product</term>
<term>Pyridine</term>
<term>Pyridine ring</term>
<term>Reaction mixture</term>
<term>Reflux</term>
<term>Sbcl5</term>
<term>Sbf3</term>
<term>Schlosser</term>
<term>Sodium hydroxide</term>
<term>Sodium sulfate</term>
<term>Sulfate</term>
<term>Tetrabutylammonium fluoride</term>
<term>Thiophosgene</term>
<term>Toluene</term>
<term>Trifluoromethoxy</term>
<term>Verlag</term>
<term>Verlag gmbh</term>
<term>Weinheim</term>
<term>White powder</term>
<term>Yellow solution</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.</div>
</front>
</TEI>
<istex>
<corpusName>wiley</corpusName>
<keywords>
<teeft>
<json:string>mmol</json:string>
<json:string>equiv</json:string>
<json:string>cdcl3</json:string>
<json:string>dropwise</json:string>
<json:string>reaction mixture</json:string>
<json:string>sodium sulfate</json:string>
<json:string>sulfate</json:string>
<json:string>organic layers</json:string>
<json:string>ocf3</json:string>
<json:string>chem</json:string>
<json:string>calcd</json:string>
<json:string>diethyl</json:string>
<json:string>ethyl acetate</json:string>
<json:string>diethyl ether</json:string>
<json:string>hydroxide</json:string>
<json:string>hydrochloric</json:string>
<json:string>hydrochloric acid</json:string>
<json:string>mbar</json:string>
<json:string>pyridine</json:string>
<json:string>butyllithium</json:string>
<json:string>hexane</json:string>
<json:string>aqueous layer</json:string>
<json:string>weinheim</json:string>
<json:string>dichloromethane</json:string>
<json:string>colorless needles</json:string>
<json:string>chloroform</json:string>
<json:string>verlag gmbh</json:string>
<json:string>kgaa</json:string>
<json:string>verlag</json:string>
<json:string>gmbh</json:string>
<json:string>crude product</json:string>
<json:string>ether</json:string>
<json:string>filtrate</json:string>
<json:string>cooh</json:string>
<json:string>sodium hydroxide</json:string>
<json:string>leroux</json:string>
<json:string>aqueous solution</json:string>
<json:string>cd3od</json:string>
<json:string>diisopropylamine</json:string>
<json:string>pure product</json:string>
<json:string>excess chlorine</json:string>
<json:string>eluent</json:string>
<json:string>trifluoromethoxy</json:string>
<json:string>methoxy</json:string>
<json:string>full paper</json:string>
<json:string>reflux</json:string>
<json:string>toluene</json:string>
<json:string>pure acid</json:string>
<json:string>sbf3</json:string>
<json:string>methanol</json:string>
<json:string>carbonate</json:string>
<json:string>aqueous sodium hydroxide</json:string>
<json:string>formate</json:string>
<json:string>dropwise addition</json:string>
<json:string>sbcl5</json:string>
<json:string>azide</json:string>
<json:string>ammonium formate</json:string>
<json:string>ocf2cl</json:string>
<json:string>thiophosgene</json:string>
<json:string>benzenesulfonyl</json:string>
<json:string>colorless</json:string>
<json:string>benzenesulfonyl azide</json:string>
<json:string>hrms</json:string>
<json:string>yellow solution</json:string>
<json:string>cyclohexane</json:string>
<json:string>propionitrile</json:string>
<json:string>occl3</json:string>
<json:string>schlosser</json:string>
<json:string>colorless powder</json:string>
<json:string>ammonium</json:string>
<json:string>aqueous sodium hydrogen carbonate</json:string>
<json:string>carboxylation</json:string>
<json:string>ethyl</json:string>
<json:string>citric acid</json:string>
<json:string>ocf3 group</json:string>
<json:string>dihedral angle</json:string>
<json:string>pyridine ring</json:string>
<json:string>ocf2cl byproduct</json:string>
<json:string>white powder</json:string>
<json:string>tetrabutylammonium fluoride</json:string>
<json:string>methoxy group</json:string>
<json:string>fluorine chem</json:string>
</teeft>
</keywords>
<author>
<json:item>
<name>Baptiste Manteau</name>
<affiliations>
<json:string>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</json:string>
</affiliations>
</json:item>
<json:item>
<name>Pierre Genix</name>
<affiliations>
<json:string>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</json:string>
</affiliations>
</json:item>
<json:item>
<name>Lydia Brelot</name>
<affiliations>
<json:string>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France</json:string>
</affiliations>
</json:item>
<json:item>
<name>Jean‐Pierre Vors</name>
<affiliations>
<json:string>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</json:string>
</affiliations>
</json:item>
<json:item>
<name>Sergiy Pazenok</name>
<affiliations>
<json:string>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany</json:string>
</affiliations>
</json:item>
<json:item>
<name>Florence Giornal</name>
<affiliations>
<json:string>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</json:string>
</affiliations>
</json:item>
<json:item>
<name>Charlotte Leuenberger</name>
<affiliations>
<json:string>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</json:string>
</affiliations>
</json:item>
<json:item>
<name>Frédéric R. Leroux</name>
<affiliations>
<json:string>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</json:string>
</affiliations>
</json:item>
</author>
<subject>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>Nitrogen heterocycles</value>
</json:item>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>Fluorine</value>
</json:item>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>Organometallic intermediates</value>
</json:item>
<json:item>
<lang>
<json:string>eng</json:string>
</lang>
<value>Ab initio calculations</value>
</json:item>
</subject>
<articleId>
<json:string>EJOC201000958</json:string>
</articleId>
<language>
<json:string>eng</json:string>
</language>
<originalGenre>
<json:string>bookReview</json:string>
</originalGenre>
<abstract>The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.</abstract>
<qualityIndicators>
<score>5.816</score>
<pdfVersion>1.3</pdfVersion>
<pdfPageSize>593 x 794 pts</pdfPageSize>
<refBibsNative>true</refBibsNative>
<abstractCharCount>605</abstractCharCount>
<pdfWordCount>20725</pdfWordCount>
<pdfCharCount>113217</pdfCharCount>
<pdfPageCount>24</pdfPageCount>
<abstractWordCount>68</abstractWordCount>
</qualityIndicators>
<title>A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
<genre>
<json:string>book-reviews</json:string>
</genre>
<host>
<title>European Journal of Organic Chemistry</title>
<language>
<json:string>unknown</json:string>
</language>
<doi>
<json:string>10.1002/(ISSN)1099-0690</json:string>
</doi>
<issn>
<json:string>1434-193X</json:string>
</issn>
<eissn>
<json:string>1099-0690</json:string>
</eissn>
<publisherId>
<json:string>EJOC</json:string>
</publisherId>
<volume>2010</volume>
<issue>31</issue>
<pages>
<first>6043</first>
<last>6066</last>
<total>24</total>
</pages>
<genre>
<json:string>journal</json:string>
</genre>
<subject>
<json:item>
<value>Full Paper</value>
</json:item>
</subject>
</host>
<categories>
<wos>
<json:string>science</json:string>
<json:string>chemistry, organic</json:string>
</wos>
<scienceMetrix>
<json:string>natural sciences</json:string>
<json:string>chemistry</json:string>
<json:string>organic chemistry</json:string>
</scienceMetrix>
<inist>
<json:string>sciences appliquees, technologies et medecines</json:string>
<json:string>sciences biologiques et medicales</json:string>
<json:string>sciences biologiques fondamentales et appliquees. psychologie</json:string>
<json:string>biophysique des tissus, organes et organismes</json:string>
</inist>
</categories>
<publicationDate>2010</publicationDate>
<copyrightDate>2010</copyrightDate>
<doi>
<json:string>10.1002/ejoc.201000958</json:string>
</doi>
<id>A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5</id>
<score>1</score>
<fulltext>
<json:item>
<extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/fulltext/pdf</uri>
</json:item>
<json:item>
<extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/fulltext/tei">
<teiHeader>
<fileDesc>
<titleStmt>
<title level="a" type="main" xml:lang="en">A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
</titleStmt>
<publicationStmt>
<authority>ISTEX</authority>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<availability>
<licence>Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</licence>
</availability>
<date type="published" when="2010-11"></date>
</publicationStmt>
<notesStmt>
<note type="content-type" subtype="book-reviews" source="bookReview" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-PBH5VBM9-4">book-reviews</note>
<note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note>
</notesStmt>
<sourceDesc>
<biblStruct type="book-reviews">
<analytic>
<title level="a" type="main" xml:lang="en">A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
<title level="a" type="short" xml:lang="en">(Trifluoromethoxy)pyridines</title>
<author xml:id="author-0000">
<persName>
<forename type="first">Baptiste</forename>
<surname>Manteau</surname>
</persName>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0001">
<persName>
<forename type="first">Pierre</forename>
<surname>Genix</surname>
</persName>
<affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0002">
<persName>
<forename type="first">Lydia</forename>
<surname>Brelot</surname>
</persName>
<affiliation>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0003">
<persName>
<forename type="first">Jean‐Pierre</forename>
<surname>Vors</surname>
</persName>
<affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0004">
<persName>
<forename type="first">Sergiy</forename>
<surname>Pazenok</surname>
</persName>
<affiliation>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany
<address>
<country key="DE"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0005">
<persName>
<forename type="first">Florence</forename>
<surname>Giornal</surname>
</persName>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0006">
<persName>
<forename type="first">Charlotte</forename>
<surname>Leuenberger</surname>
</persName>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0007">
<persName>
<forename type="first">Frédéric R.</forename>
<surname>Leroux</surname>
</persName>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742
<address>
<country key="FR"></country>
</address>
</affiliation>
</author>
<idno type="istex">A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5</idno>
<idno type="ark">ark:/67375/WNG-ZQHQZ0LN-3</idno>
<idno type="DOI">10.1002/ejoc.201000958</idno>
<idno type="unit">EJOC201000958</idno>
<idno type="toTypesetVersion">file:EJOC.EJOC201000958.pdf</idno>
</analytic>
<monogr>
<title level="j" type="main">European Journal of Organic Chemistry</title>
<title level="j" type="alt">EUROPEAN JOURNAL OF ORGANIC CHEMISTRY</title>
<idno type="pISSN">1434-193X</idno>
<idno type="eISSN">1099-0690</idno>
<idno type="book-DOI">10.1002/(ISSN)1099-0690</idno>
<idno type="book-part-DOI">10.1002/ejoc.v2010:31</idno>
<idno type="product">EJOC</idno>
<imprint>
<biblScope unit="vol">2010</biblScope>
<biblScope unit="issue">31</biblScope>
<biblScope unit="page" from="6043">6043</biblScope>
<biblScope unit="page" to="6066">6066</biblScope>
<biblScope unit="page-count">24</biblScope>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="2010-11"></date>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<abstract xml:lang="en" style="main">
<head>Abstract</head>
<p>The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.</p>
</abstract>
<abstract xml:lang="en" style="graphical">
<p>A general and efficient route to (trifluoromethoxy)pyridines is reported. Regioselective functionalization by organometallic methods afforded new and highly important building blocks for life‐sciences‐oriented research. The first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed and supported by in silico studies.
<figure type="box">
<media mimeType="image" url="urn:x-wiley:1434193X:media:EJOC201000958:fig000"></media>
<media mimeType="image/gif" url="" rendition="webLoRes"></media>
<media mimeType="image/jpeg" url="" rendition="webOriginal"></media>
<media mimeType="image/jpeg" url="" rendition="webHiRes"></media>
</figure>
</p>
</abstract>
<textClass>
<keywords xml:lang="en">
<term xml:id="kwd1">Nitrogen heterocycles</term>
<term xml:id="kwd2">Fluorine</term>
<term xml:id="kwd3">Organometallic intermediates</term>
<term xml:id="kwd4">Ab initio calculations</term>
</keywords>
<keywords rend="articleCategory">
<term>Full Paper</term>
</keywords>
<keywords rend="tocHeading1">
<term>Full Papers</term>
</keywords>
<keywords rend="tocHeading2">
<term>Fluorine Chemistry</term>
</keywords>
</textClass>
<langUsage>
<language ident="en"></language>
</langUsage>
</profileDesc>
</teiHeader>
</istex:fulltextTEI>
<json:item>
<extension>txt</extension>
<original>false</original>
<mimetype>text/plain</mimetype>
<uri>https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/fulltext/txt</uri>
</json:item>
</fulltext>
<metadata>
<istex:metadataXml wicri:clean="Wiley, elements deleted: body">
<istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration>
<istex:document>
<component version="2.0" type="serialArticle" xml:lang="en">
<header>
<publicationMeta level="product">
<publisherInfo>
<publisherName>WILEY‐VCH Verlag</publisherName>
<publisherLoc>Weinheim</publisherLoc>
</publisherInfo>
<doi registered="yes">10.1002/(ISSN)1099-0690</doi>
<issn type="print">1434-193X</issn>
<issn type="electronic">1099-0690</issn>
<idGroup>
<id type="product" value="EJOC"></id>
</idGroup>
<titleGroup>
<title type="main" xml:lang="en" sort="EUROPEAN JOURNAL OF ORGANIC CHEMISTRY">European Journal of Organic Chemistry</title>
<title type="short">Eur. J. Org. Chem.</title>
</titleGroup>
</publicationMeta>
<publicationMeta level="part" position="310">
<doi origin="wiley" registered="yes">10.1002/ejoc.v2010:31</doi>
<numberingGroup>
<numbering type="journalVolume" number="2010">2010</numbering>
<numbering type="journalIssue">31</numbering>
</numberingGroup>
<coverDate startDate="2010-11">November 2010</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="bookReview" position="18" status="forIssue">
<doi origin="wiley" registered="yes">10.1002/ejoc.201000958</doi>
<idGroup>
<id type="unit" value="EJOC201000958"></id>
</idGroup>
<countGroup>
<count type="pageTotal" number="24"></count>
</countGroup>
<titleGroup>
<title type="articleCategory">Full Paper</title>
<title type="tocHeading1">Full Papers</title>
<title type="tocHeading2">Fluorine Chemistry</title>
</titleGroup>
<copyright ownership="publisher">Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</copyright>
<eventGroup>
<event type="manuscriptReceived" date="2010-07-07"></event>
<event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.4.4 mode:FullText" date="2011-02-02"></event>
<event type="publishedOnlineEarlyUnpaginated" date="2010-09-14"></event>
<event type="publishedOnlineFinalForm" date="2010-10-19"></event>
<event type="firstOnline" date="2010-09-14"></event>
<event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-24"></event>
<event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-16"></event>
</eventGroup>
<numberingGroup>
<numbering type="pageFirst">6043</numbering>
<numbering type="pageLast">6066</numbering>
</numberingGroup>
<objectNameGroup>
<objectName elementName="figure">Scheme</objectName>
</objectNameGroup>
<linkGroup>
<link type="toTypesetVersion" href="file:EJOC.EJOC201000958.pdf"></link>
</linkGroup>
</publicationMeta>
<contentMeta>
<countGroup>
<count type="figureTotal" number="7"></count>
<count type="tableTotal" number="3"></count>
<count type="referenceTotal" number="30"></count>
</countGroup>
<titleGroup>
<title type="main" xml:lang="en">A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
<title type="short" xml:lang="en">(Trifluoromethoxy)pyridines</title>
</titleGroup>
<creators>
<creator xml:id="au1" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Baptiste</givenNames>
<familyName>Manteau</familyName>
</personName>
</creator>
<creator xml:id="au2" creatorRole="author" affiliationRef="#af2">
<personName>
<givenNames>Pierre</givenNames>
<familyName>Genix</familyName>
</personName>
</creator>
<creator xml:id="au3" creatorRole="author" affiliationRef="#af3">
<personName>
<givenNames>Lydia</givenNames>
<familyName>Brelot</familyName>
</personName>
</creator>
<creator xml:id="au4" creatorRole="author" affiliationRef="#af2">
<personName>
<givenNames>Jean‐Pierre</givenNames>
<familyName>Vors</familyName>
</personName>
</creator>
<creator xml:id="au5" creatorRole="author" affiliationRef="#af4">
<personName>
<givenNames>Sergiy</givenNames>
<familyName>Pazenok</familyName>
</personName>
</creator>
<creator xml:id="au6" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Florence</givenNames>
<familyName>Giornal</familyName>
</personName>
</creator>
<creator xml:id="au7" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Charlotte</givenNames>
<familyName>Leuenberger</familyName>
</personName>
</creator>
<creator xml:id="au8" creatorRole="author" affiliationRef="#af1">
<personName>
<givenNames>Frédéric R.</givenNames>
<familyName>Leroux</familyName>
</personName>
</creator>
</creators>
<affiliationGroup>
<affiliation xml:id="af1" countryCode="FR" type="organization">
<unparsedAffiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</unparsedAffiliation>
</affiliation>
<affiliation xml:id="af2" countryCode="FR" type="organization">
<unparsedAffiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</unparsedAffiliation>
</affiliation>
<affiliation xml:id="af3" countryCode="FR" type="organization">
<unparsedAffiliation>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France</unparsedAffiliation>
</affiliation>
<affiliation xml:id="af4" countryCode="DE" type="organization">
<unparsedAffiliation>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en" type="author">
<keyword xml:id="kwd1">Nitrogen heterocycles</keyword>
<keyword xml:id="kwd2">Fluorine</keyword>
<keyword xml:id="kwd3">Organometallic intermediates</keyword>
<keyword xml:id="kwd4">Ab initio calculations</keyword>
</keywordGroup>
<fundingInfo>
<fundingAgency>Ministère de la Recherche of France</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>Centre National de la Recherche Scientifique (CNRS)</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>Bayer CropScience</fundingAgency>
</fundingInfo>
<supportingInformation>
<p>Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer‐reviewed, but not copy‐edited or typeset. They are made available as submitted by the authors. </p>
<supportingInfoItem>
<mediaResource alt="supporting information" href="urn-x:wiley:1434193X:media:ejoc201000958:ejoc_201000958_sm_miscellaneous_information"></mediaResource>
<caption>miscellaneous_information</caption>
</supportingInfoItem>
</supportingInformation>
<abstractGroup>
<abstract type="main" xml:lang="en">
<title type="main">Abstract</title>
<p>The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.</p>
</abstract>
<abstract type="graphical" xml:lang="en">
<p>A general and efficient route to (trifluoromethoxy)pyridines is reported. Regioselective functionalization by organometallic methods afforded new and highly important building blocks for life‐sciences‐oriented research. The first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed and supported by in silico studies.
<blockFixed type="graphic">
<mediaResourceGroup>
<mediaResource alt="image" eRights="yes" copyright="WILEY-VCH" href="urn:x-wiley:1434193X:media:EJOC201000958:fig000"></mediaResource>
<mediaResource alt="thumbnail image" rendition="webLoRes" mimeType="image/gif" href=""></mediaResource>
<mediaResource alt="original image" rendition="webOriginal" mimeType="image/jpeg" href=""></mediaResource>
<mediaResource alt="magnified image" rendition="webHiRes" mimeType="image/jpeg" href=""></mediaResource>
</mediaResourceGroup>
</blockFixed>
</p>
</abstract>
</abstractGroup>
</contentMeta>
</header>
</component>
</istex:document>
</istex:metadataXml>
<mods version="3.6">
<titleInfo lang="en">
<title>A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
</titleInfo>
<titleInfo type="abbreviated" lang="en">
<title>(Trifluoromethoxy)pyridines</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en">
<title>A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies</title>
</titleInfo>
<name type="personal">
<namePart type="given">Baptiste</namePart>
<namePart type="family">Manteau</namePart>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Pierre</namePart>
<namePart type="family">Genix</namePart>
<affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Lydia</namePart>
<namePart type="family">Brelot</namePart>
<affiliation>Service de Radiocristallographie, Institut de Chimie UMR 7177, CNRS‐Université de Strasbourg, Bâtiment Le Bel, 4 rue Blaise Pascal, 67070 Strasbourg, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Jean‐Pierre</namePart>
<namePart type="family">Vors</namePart>
<affiliation>Centre de Recherches de la Dargoire, Bayer SAS, Bayer CropScience, 14 Impasse Pierre Baizet, 69009 Lyon, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Sergiy</namePart>
<namePart type="family">Pazenok</namePart>
<affiliation>Bayer CropScience AG, Alfred‐Nobel‐Strasse 50, 40789 Monheim, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Florence</namePart>
<namePart type="family">Giornal</namePart>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Charlotte</namePart>
<namePart type="family">Leuenberger</namePart>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Frédéric R.</namePart>
<namePart type="family">Leroux</namePart>
<affiliation>CNRS/Université de Strasbourg, UMR CNRS 7509, ECPM, 25 rue Becquerel, 67087 Strasbourg, France, Fax: +33‐3‐68852742</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre type="book-reviews" displayLabel="bookReview" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-PBH5VBM9-4">book-reviews</genre>
<originInfo>
<publisher>WILEY‐VCH Verlag</publisher>
<place>
<placeTerm type="text">Weinheim</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2010-11</dateIssued>
<dateCaptured encoding="w3cdtf">2010-07-07</dateCaptured>
<copyrightDate encoding="w3cdtf">2010</copyrightDate>
</originInfo>
<language>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription>
<extent unit="figures">7</extent>
<extent unit="tables">3</extent>
<extent unit="references">30</extent>
</physicalDescription>
<abstract lang="en">The previously unknown 2‐, 3‐, and 4‐(trifluoromethoxy)pyridines have now become readily accessible by means of an efficient and straightforward large‐scale synthesis. Their regioselective functionalization by organometallic methods has been studied and has afforded new and highly important building blocks for life‐sciences‐oriented research. In addition, the first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed. Lowest‐energy conformations of (trifluoromethoxy)pyridines and (trifluoromethoxy)pyridinium cations were determined by in silico studies.</abstract>
<abstract type="graphical" lang="en">A general and efficient route to (trifluoromethoxy)pyridines is reported. Regioselective functionalization by organometallic methods afforded new and highly important building blocks for life‐sciences‐oriented research. The first X‐ray crystallographic structure determinations of (trifluoromethoxy)pyridines have been performed and supported by in silico studies.</abstract>
<note type="funding">Ministère de la Recherche of France</note>
<note type="funding">Centre National de la Recherche Scientifique (CNRS)</note>
<note type="funding">Bayer CropScience</note>
<subject lang="en">
<genre>keywords</genre>
<topic>Nitrogen heterocycles</topic>
<topic>Fluorine</topic>
<topic>Organometallic intermediates</topic>
<topic>Ab initio calculations</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>European Journal of Organic Chemistry</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Eur. J. Org. Chem.</title>
</titleInfo>
<genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre>
<note type="content"> Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer‐reviewed, but not copy‐edited or typeset. They are made available as submitted by the authors.Supporting Info Item: miscellaneous_information - </note>
<subject>
<genre>article-category</genre>
<topic>Full Paper</topic>
</subject>
<identifier type="ISSN">1434-193X</identifier>
<identifier type="eISSN">1099-0690</identifier>
<identifier type="DOI">10.1002/(ISSN)1099-0690</identifier>
<identifier type="PublisherID">EJOC</identifier>
<part>
<date>2010</date>
<detail type="volume">
<caption>vol.</caption>
<number>2010</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>31</number>
</detail>
<extent unit="pages">
<start>6043</start>
<end>6066</end>
<total>24</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5</identifier>
<identifier type="ark">ark:/67375/WNG-ZQHQZ0LN-3</identifier>
<identifier type="DOI">10.1002/ejoc.201000958</identifier>
<identifier type="ArticleID">EJOC201000958</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</accessCondition>
<recordInfo>
<recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource>
<recordOrigin>WILEY‐VCH Verlag</recordOrigin>
</recordInfo>
</mods>
<json:item>
<extension>json</extension>
<original>false</original>
<mimetype>application/json</mimetype>
<uri>https://api.istex.fr/document/A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5/metadata/json</uri>
</json:item>
</metadata>
<serie></serie>
</istex>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Lorraine/explor/LrgpV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001308 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 001308 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Lorraine
   |area=    LrgpV1
   |flux=    Istex
   |étape=   Corpus
   |type=    RBID
   |clé=     ISTEX:A471E7D4C151D5F3D7577A8EC716C0E331E2B0D5
   |texte=   A General Approach to (Trifluoromethoxy)pyridines: First X‐ray Structure Determinations and Quantum Chemistry Studies
}}

Wicri

This area was generated with Dilib version V0.6.32.
Data generation: Sat Nov 11 15:47:48 2017. Site generation: Wed Mar 6 23:31:34 2024