ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.
Identifieur interne : 000279 ( Istex/Corpus ); précédent : 000278; suivant : 000280ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.
Auteurs : G. Bartoli ; M. Bosco ; A. Guerrieri ; R. Dalpozzo ; A. De Nino ; E. Iantorno ; G. PalmieriSource :
- ChemInform [ 0931-7597 ] ; 1996-07-02.
English descriptors
- KwdEn :
- Acyclic, Arcavacata, Carbonate, Chim, Dalpozzo, Dianion, Dianion formation, Dianions, Diethyl, Diethyl carbonate, Enamino, Enamino ketones, Enaminone, Enaminone dianions, Ester, Gazz, Guerrieri, Iantorno, Intermediates intermediates, Ital, Ketone, Ltmp, Metalation, Nino, Palmieri, Polyoxo, Polyoxo acids, Potential intermediates, Rende, Trophiles, Univ.
- Teeft :
- Acyclic, Arcavacata, Carbonate, Chim, Dalpozzo, Dianion, Dianion formation, Dianions, Diethyl, Diethyl carbonate, Enamino, Enamino ketones, Enaminone, Enaminone dianions, Ester, Gazz, Guerrieri, Iantorno, Intermediates intermediates, Ital, Ketone, Ltmp, Metalation, Nino, Palmieri, Polyoxo, Polyoxo acids, Potential intermediates, Rende, Trophiles, Univ.
Abstract
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Url:
DOI: 10.1002/chin.199627069
Links to Exploration step
ISTEX:860065135731B0884D826B6F36A4A604DEA7A028Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
<author><name sortKey="Bartoli, G" sort="Bartoli, G" uniqKey="Bartoli G" first="G." last="Bartoli">G. Bartoli</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Bosco, M" sort="Bosco, M" uniqKey="Bosco M" first="M." last="Bosco">M. Bosco</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Guerrieri, A" sort="Guerrieri, A" uniqKey="Guerrieri A" first="A." last="Guerrieri">A. Guerrieri</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Dalpozzo, R" sort="Dalpozzo, R" uniqKey="Dalpozzo R" first="R." last="Dalpozzo">R. Dalpozzo</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="De Nino, A" sort="De Nino, A" uniqKey="De Nino A" first="A." last="De Nino">A. De Nino</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Iantorno, E" sort="Iantorno, E" uniqKey="Iantorno E" first="E." last="Iantorno">E. Iantorno</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Palmieri, G" sort="Palmieri, G" uniqKey="Palmieri G" first="G." last="Palmieri">G. Palmieri</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:860065135731B0884D826B6F36A4A604DEA7A028</idno>
<date when="1996" year="1996">1996</date>
<idno type="doi">10.1002/chin.199627069</idno>
<idno type="url">https://api.istex.fr/document/860065135731B0884D826B6F36A4A604DEA7A028/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000279</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000279</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
<author><name sortKey="Bartoli, G" sort="Bartoli, G" uniqKey="Bartoli G" first="G." last="Bartoli">G. Bartoli</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Bosco, M" sort="Bosco, M" uniqKey="Bosco M" first="M." last="Bosco">M. Bosco</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Guerrieri, A" sort="Guerrieri, A" uniqKey="Guerrieri A" first="A." last="Guerrieri">A. Guerrieri</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Dalpozzo, R" sort="Dalpozzo, R" uniqKey="Dalpozzo R" first="R." last="Dalpozzo">R. Dalpozzo</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="De Nino, A" sort="De Nino, A" uniqKey="De Nino A" first="A." last="De Nino">A. De Nino</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Iantorno, E" sort="Iantorno, E" uniqKey="Iantorno E" first="E." last="Iantorno">E. Iantorno</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Palmieri, G" sort="Palmieri, G" uniqKey="Palmieri G" first="G." last="Palmieri">G. Palmieri</name>
<affiliation><mods:affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</mods:affiliation>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">ChemInform</title>
<title level="j" type="alt">CHEMINFORM</title>
<idno type="ISSN">0931-7597</idno>
<idno type="eISSN">1522-2667</idno>
<imprint><biblScope unit="vol">27</biblScope>
<biblScope unit="issue">27</biblScope>
<biblScope unit="page" from="no">no</biblScope>
<biblScope unit="page" to="no">no</biblScope>
<biblScope unit="page-count">1</biblScope>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="1996-07-02">1996-07-02</date>
</imprint>
<idno type="ISSN">0931-7597</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0931-7597</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acyclic</term>
<term>Arcavacata</term>
<term>Carbonate</term>
<term>Chim</term>
<term>Dalpozzo</term>
<term>Dianion</term>
<term>Dianion formation</term>
<term>Dianions</term>
<term>Diethyl</term>
<term>Diethyl carbonate</term>
<term>Enamino</term>
<term>Enamino ketones</term>
<term>Enaminone</term>
<term>Enaminone dianions</term>
<term>Ester</term>
<term>Gazz</term>
<term>Guerrieri</term>
<term>Iantorno</term>
<term>Intermediates intermediates</term>
<term>Ital</term>
<term>Ketone</term>
<term>Ltmp</term>
<term>Metalation</term>
<term>Nino</term>
<term>Palmieri</term>
<term>Polyoxo</term>
<term>Polyoxo acids</term>
<term>Potential intermediates</term>
<term>Rende</term>
<term>Trophiles</term>
<term>Univ</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Acyclic</term>
<term>Arcavacata</term>
<term>Carbonate</term>
<term>Chim</term>
<term>Dalpozzo</term>
<term>Dianion</term>
<term>Dianion formation</term>
<term>Dianions</term>
<term>Diethyl</term>
<term>Diethyl carbonate</term>
<term>Enamino</term>
<term>Enamino ketones</term>
<term>Enaminone</term>
<term>Enaminone dianions</term>
<term>Ester</term>
<term>Gazz</term>
<term>Guerrieri</term>
<term>Iantorno</term>
<term>Intermediates intermediates</term>
<term>Ital</term>
<term>Ketone</term>
<term>Ltmp</term>
<term>Metalation</term>
<term>Nino</term>
<term>Palmieri</term>
<term>Polyoxo</term>
<term>Polyoxo acids</term>
<term>Potential intermediates</term>
<term>Rende</term>
<term>Trophiles</term>
<term>Univ</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</div>
</front>
</TEI>
<istex><corpusName>wiley</corpusName>
<keywords><teeft><json:string>ester</json:string>
<json:string>dianions</json:string>
<json:string>enamino</json:string>
<json:string>ketone</json:string>
<json:string>enamino ketones</json:string>
<json:string>ltmp</json:string>
<json:string>chim</json:string>
<json:string>carbonate</json:string>
<json:string>metalation</json:string>
<json:string>intermediates intermediates</json:string>
<json:string>dianion</json:string>
<json:string>dianion formation</json:string>
<json:string>enaminone</json:string>
<json:string>enaminone dianions</json:string>
<json:string>diethyl</json:string>
<json:string>trophiles</json:string>
<json:string>diethyl carbonate</json:string>
<json:string>potential intermediates</json:string>
<json:string>polyoxo</json:string>
<json:string>polyoxo acids</json:string>
<json:string>guerrieri</json:string>
<json:string>dalpozzo</json:string>
<json:string>nino</json:string>
<json:string>iantorno</json:string>
<json:string>palmieri</json:string>
<json:string>gazz</json:string>
<json:string>acyclic</json:string>
<json:string>ital</json:string>
<json:string>univ</json:string>
<json:string>arcavacata</json:string>
<json:string>rende</json:string>
</teeft>
</keywords>
<author><json:item><name>G. BARTOLI</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>M. BOSCO</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>A. GUERRIERI</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>R. DALPOZZO</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>A. DE NINO</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>E. IANTORNO</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
<json:item><name>G. PALMIERI</name>
<affiliations><json:string>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</json:string>
</affiliations>
</json:item>
</author>
<subject><json:item><lang><json:string>eng</json:string>
</lang>
<value>intermediates (and their reactions)</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>carboxylation, decarboxylation</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>substitution reactions</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>oxocarboxylic acids and esters (acyclic compounds)</value>
</json:item>
</subject>
<articleId><json:string>CHIN199627069</json:string>
</articleId>
<language><json:string>eng</json:string>
</language>
<originalGenre><json:string>article</json:string>
</originalGenre>
<abstract>ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</abstract>
<qualityIndicators><score>1.176</score>
<pdfVersion>1.4</pdfVersion>
<pdfPageSize>595.276 x 841.89 pts (A4)</pdfPageSize>
<refBibsNative>true</refBibsNative>
<abstractCharCount>314</abstractCharCount>
<pdfWordCount>112</pdfWordCount>
<pdfCharCount>744</pdfCharCount>
<pdfPageCount>1</pdfPageCount>
<abstractWordCount>47</abstractWordCount>
</qualityIndicators>
<title>ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
<genre><json:string>article</json:string>
</genre>
<host><title>ChemInform</title>
<language><json:string>unknown</json:string>
</language>
<doi><json:string>10.1002/(ISSN)1522-2667</json:string>
</doi>
<issn><json:string>0931-7597</json:string>
</issn>
<eissn><json:string>1522-2667</json:string>
</eissn>
<publisherId><json:string>CHIN</json:string>
</publisherId>
<volume>27</volume>
<issue>27</issue>
<genre><json:string>journal</json:string>
</genre>
<subject><json:item><value>Preparative Organic Chemistry</value>
</json:item>
</subject>
</host>
<categories><inist><json:string>sciences appliquees, technologies et medecines</json:string>
<json:string>sciences biologiques et medicales</json:string>
<json:string>sciences medicales</json:string>
</inist>
</categories>
<publicationDate>1996</publicationDate>
<copyrightDate>1996</copyrightDate>
<doi><json:string>10.1002/chin.199627069</json:string>
</doi>
<id>860065135731B0884D826B6F36A4A604DEA7A028</id>
<score>1</score>
<fulltext><json:item><extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/document/860065135731B0884D826B6F36A4A604DEA7A028/fulltext/pdf</uri>
</json:item>
<json:item><extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/document/860065135731B0884D826B6F36A4A604DEA7A028/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/860065135731B0884D826B6F36A4A604DEA7A028/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
</titleStmt>
<publicationStmt><authority>ISTEX</authority>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<availability><licence>Copyright © 1996 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</licence>
</availability>
<date type="published" when="1996-07-02"></date>
</publicationStmt>
<notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</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="article"><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
<author xml:id="author-0000"><persName><forename type="first">G.</forename>
<surname>BARTOLI</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0001"><persName><forename type="first">M.</forename>
<surname>BOSCO</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0002"><persName><forename type="first">A.</forename>
<surname>GUERRIERI</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0003"><persName><forename type="first">R.</forename>
<surname>DALPOZZO</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0004"><persName><forename type="first">A.</forename>
<surname>DE NINO</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0005"><persName><forename type="first">E.</forename>
<surname>IANTORNO</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0006"><persName><forename type="first">G.</forename>
<surname>PALMIERI</surname>
</persName>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy<address><country key="IT"></country>
</address>
</affiliation>
</author>
<idno type="istex">860065135731B0884D826B6F36A4A604DEA7A028</idno>
<idno type="ark">ark:/67375/WNG-2VJNV95V-H</idno>
<idno type="DOI">10.1002/chin.199627069</idno>
<idno type="unit">CHIN199627069</idno>
<idno type="toTypesetVersion">file:CHIN.CHIN199627069.pdf</idno>
</analytic>
<monogr><title level="j" type="main">ChemInform</title>
<title level="j" type="alt">CHEMINFORM</title>
<idno type="pISSN">0931-7597</idno>
<idno type="eISSN">1522-2667</idno>
<idno type="book-DOI">10.1002/(ISSN)1522-2667</idno>
<idno type="book-part-DOI">10.1002/chin.v27:27</idno>
<idno type="product">CHIN</idno>
<imprint><biblScope unit="vol">27</biblScope>
<biblScope unit="issue">27</biblScope>
<biblScope unit="page" from="no">no</biblScope>
<biblScope unit="page" to="no">no</biblScope>
<biblScope unit="page-count">1</biblScope>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<date type="published" when="1996-07-02"></date>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head>
<p>ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</p>
</abstract>
<textClass><keywords xml:lang="en"><term xml:id="kwd1">intermediates (and their reactions)</term>
<term xml:id="kwd2">carboxylation, decarboxylation</term>
<term xml:id="kwd3">substitution reactions</term>
<term xml:id="kwd4">oxocarboxylic acids and esters (acyclic compounds)</term>
</keywords>
<keywords rend="articleCategory"><term>Preparative Organic Chemistry</term>
</keywords>
<keywords rend="tocHeading1"><term>Preparative Organic 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/860065135731B0884D826B6F36A4A604DEA7A028/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)1522-2667</doi>
<issn type="print">0931-7597</issn>
<issn type="electronic">1522-2667</issn>
<idGroup><id type="product" value="CHIN"></id>
</idGroup>
<titleGroup><title type="main" xml:lang="en" sort="CHEMINFORM">ChemInform</title>
<title type="short">ChemInform</title>
</titleGroup>
</publicationMeta>
<publicationMeta level="part" position="270"><doi origin="wiley" registered="yes">10.1002/chin.v27:27</doi>
<numberingGroup><numbering type="journalVolume" number="27">27</numbering>
<numbering type="journalIssue">27</numbering>
</numberingGroup>
<coverDate startDate="1996-07-02">July 2, 1996</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="article" position="69" status="forIssue"><doi origin="wiley" registered="yes">10.1002/chin.199627069</doi>
<idGroup><id type="unit" value="CHIN199627069"></id>
</idGroup>
<countGroup><count type="pageTotal" number="1"></count>
</countGroup>
<titleGroup><title type="articleCategory">Preparative Organic Chemistry</title>
<title type="tocHeading1">Preparative Organic Chemistry</title>
</titleGroup>
<copyright ownership="publisher">Copyright © 1996 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</copyright>
<eventGroup><event type="firstOnline" date="2010-08-05"></event>
<event type="publishedOnlineFinalForm" date="2010-08-05"></event>
<event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.15 mode:FullText source:FullText result:FullText" date="2010-08-13"></event>
<event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-10"></event>
<event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-15"></event>
</eventGroup>
<numberingGroup><numbering type="pageFirst">no</numbering>
<numbering type="pageLast">no</numbering>
</numberingGroup>
<linkGroup><link type="toTypesetVersion" href="file:CHIN.CHIN199627069.pdf"></link>
</linkGroup>
</publicationMeta>
<contentMeta><countGroup><count type="figureTotal" number="1"></count>
<count type="tableTotal" number="0"></count>
<count type="referenceTotal" number="1"></count>
</countGroup>
<titleGroup><title type="main" xml:lang="en">ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
</titleGroup>
<creators><creator xml:id="au1" creatorRole="author" affiliationRef="#a1"><personName><givenNames>G.</givenNames>
<familyName>BARTOLI</familyName>
</personName>
</creator>
<creator xml:id="au2" creatorRole="author" affiliationRef="#a1"><personName><givenNames>M.</givenNames>
<familyName>BOSCO</familyName>
</personName>
</creator>
<creator xml:id="au3" creatorRole="author" affiliationRef="#a1"><personName><givenNames>A.</givenNames>
<familyName>GUERRIERI</familyName>
</personName>
</creator>
<creator xml:id="au4" creatorRole="author" affiliationRef="#a1"><personName><givenNames>R.</givenNames>
<familyName>DALPOZZO</familyName>
</personName>
</creator>
<creator xml:id="au5" creatorRole="author" affiliationRef="#a1"><personName><givenNames>A.</givenNames>
<familyName>DE NINO</familyName>
</personName>
</creator>
<creator xml:id="au6" creatorRole="author" affiliationRef="#a1"><personName><givenNames>E.</givenNames>
<familyName>IANTORNO</familyName>
</personName>
</creator>
<creator xml:id="au7" creatorRole="author" affiliationRef="#a1"><personName><givenNames>G.</givenNames>
<familyName>PALMIERI</familyName>
</personName>
</creator>
</creators>
<affiliationGroup><affiliation xml:id="a1" countryCode="IT" type="organization"><unparsedAffiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">intermediates (and their reactions)</keyword>
<keyword xml:id="kwd2">carboxylation, decarboxylation</keyword>
<keyword xml:id="kwd3">substitution reactions</keyword>
<keyword xml:id="kwd4">oxocarboxylic acids and esters (acyclic compounds)</keyword>
</keywordGroup>
<abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title>
<p>ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</p>
</abstract>
</abstractGroup>
</contentMeta>
</header>
</component>
</istex:document>
</istex:metadataXml>
<mods version="3.6"><titleInfo lang="en"><title>ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en"><title>ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters.</title>
</titleInfo>
<name type="personal"><namePart type="given">G.</namePart>
<namePart type="family">BARTOLI</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">M.</namePart>
<namePart type="family">BOSCO</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">A.</namePart>
<namePart type="family">GUERRIERI</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">R.</namePart>
<namePart type="family">DALPOZZO</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">A.</namePart>
<namePart type="family">DE NINO</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">E.</namePart>
<namePart type="family">IANTORNO</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">G.</namePart>
<namePart type="family">PALMIERI</namePart>
<affiliation>Dip. Chim., Univ. Calabria, I‐87030 Arcavacata di Rende, Italy</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<typeOfResource>text</typeOfResource>
<genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre>
<originInfo><publisher>WILEY‐VCH Verlag</publisher>
<place><placeTerm type="text">Weinheim</placeTerm>
</place>
<dateIssued encoding="w3cdtf">1996-07-02</dateIssued>
<copyrightDate encoding="w3cdtf">1996</copyrightDate>
</originInfo>
<language><languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
</language>
<physicalDescription><extent unit="figures">1</extent>
<extent unit="tables">0</extent>
<extent unit="references">1</extent>
</physicalDescription>
<abstract lang="en">ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</abstract>
<subject lang="en"><genre>keywords</genre>
<topic>intermediates (and their reactions)</topic>
<topic>carboxylation, decarboxylation</topic>
<topic>substitution reactions</topic>
<topic>oxocarboxylic acids and esters (acyclic compounds)</topic>
</subject>
<relatedItem type="host"><titleInfo><title>ChemInform</title>
</titleInfo>
<titleInfo type="abbreviated"><title>ChemInform</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>
<subject><genre>article-category</genre>
<topic>Preparative Organic Chemistry</topic>
</subject>
<identifier type="ISSN">0931-7597</identifier>
<identifier type="eISSN">1522-2667</identifier>
<identifier type="DOI">10.1002/(ISSN)1522-2667</identifier>
<identifier type="PublisherID">CHIN</identifier>
<part><date>1996</date>
<detail type="volume"><caption>vol.</caption>
<number>27</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>27</number>
</detail>
<extent unit="pages"><total>1</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">860065135731B0884D826B6F36A4A604DEA7A028</identifier>
<identifier type="ark">ark:/67375/WNG-2VJNV95V-H</identifier>
<identifier type="DOI">10.1002/chin.199627069</identifier>
<identifier type="ArticleID">CHIN199627069</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 1996 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/860065135731B0884D826B6F36A4A604DEA7A028/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 000279 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 000279 | 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:860065135731B0884D826B6F36A4A604DEA7A028 |texte= ChemInform Abstract: Reaction of Dianions of Acyclic β‐Enamino Ketones with Electrophiles. Part 7. Synthesis of 5‐(Monoalkylamino)‐3‐oxo γ,. delta.‐Unsaturated Acids and Esters and of 3‐(Monoalkylamino)‐5‐oxo . beta.,γ‐Unsaturated Esters. }}
![]() | This area was generated with Dilib version V0.6.32. | ![]() |