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
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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. 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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. 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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. 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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. 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