An unexpected synthesis of thiophene derivatives by thionation of N‐phenylacetylthiobenzamides
Identifieur interne : 003B52 ( Istex/Corpus ); précédent : 003B51; suivant : 003B53An unexpected synthesis of thiophene derivatives by thionation of N‐phenylacetylthiobenzamides
Auteurs : Long I Lai ; David H. Reid ; Sue Ein Wang ; Fen Ing LiaoSource :
- Heteroatom Chemistry [ 1042-7163 ] ; 1994-09.
Abstract
Four thiophene derivatives have been obtained unexpectedly from the reaction of N‐phenylacetyithiobenzamides with P4S10 in boiling carbon disulfide. The structure of one of these was established by X‐ray crystallography.
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DOI: 10.1002/hc.520050510
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Reid</name><affiliation><mods:affiliation>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</mods:affiliation></affiliation></author><author><name sortKey="Wang, Sue Ein" sort="Wang, Sue Ein" uniqKey="Wang S" first="Sue Ein" last="Wang">Sue Ein Wang</name><affiliation><mods:affiliation>Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China</mods:affiliation></affiliation></author><author><name sortKey="Liao, Fen Ing" sort="Liao, Fen Ing" uniqKey="Liao F" first="Fen Ing" last="Liao">Fen Ing Liao</name><affiliation><mods:affiliation>Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:D3913F19A10D496B57DEDDA034EEEF140056AEDC</idno><date when="1994" year="1994">1994</date><idno type="doi">10.1002/hc.520050510</idno><idno type="url">https://api.istex.fr/document/D3913F19A10D496B57DEDDA034EEEF140056AEDC/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">003B52</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">An unexpected synthesis of thiophene derivatives by thionation of N‐phenylacetylthiobenzamides</title><author><name sortKey="Lai, Long I" sort="Lai, Long I" uniqKey="Lai L" first="Long I" last="Lai">Long I Lai</name><affiliation><mods:affiliation>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</mods:affiliation></affiliation><affiliation><mods:affiliation>Current Address: Institute of Chemistry, Academia Sinica, Nankang, Taipei, 11529 Republic of China</mods:affiliation></affiliation></author><author><name sortKey="Reid, David H" sort="Reid, David H" uniqKey="Reid D" first="David H." last="Reid">David H. 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type="pageLast">486</numbering></numberingGroup><correspondenceTo>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:HC.hc520050510.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="1"></count><count type="tableTotal" number="8"></count><count type="referenceTotal" number="14"></count></countGroup><titleGroup><title type="main" xml:lang="en">An unexpected synthesis of thiophene derivatives by thionation of <i>N</i>‐phenylacetylthiobenzamides<link href="#fn1"></link></title><title type="short" xml:lang="en">An Unexpected Synthesis of Thiophene Derivatives by Thionation of <fi>N</fi>‐Phenylacetylthiobenzamides</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" currentRef="#curr1"><personName><givenNames>Long‐Li</givenNames><familyName>Lai</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>David H.</givenNames><familyName>Reid</familyName></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Sue‐Lein</givenNames><familyName>Wang</familyName></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Fen‐Ling</givenNames><familyName>Liao</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="ZA" type="organization"><unparsedAffiliation>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="CN" type="organization"><unparsedAffiliation>Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China</unparsedAffiliation></affiliation><affiliation xml:id="curr1" countryCode="CN"><unparsedAffiliation>Institute of Chemistry, Academia Sinica, Nankang, Taipei, 11529 Republic of China</unparsedAffiliation></affiliation></affiliationGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Four thiophene derivatives have been obtained unexpectedly from the reaction of N‐phenylacetyithiobenzamides with P<sub>4</sub>S<sub>10</sub> in boiling carbon disulfide. The structure of one of these was established by X‐ray crystallography.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p>Studies of Heterocyclic Compounds, Part 33.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>An unexpected synthesis of thiophene derivatives by thionation of N‐phenylacetylthiobenzamides</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>An Unexpected Synthesis of Thiophene Derivatives by Thionation of N‐Phenylacetylthiobenzamides</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>An unexpected synthesis of thiophene derivatives by thionation of</title></titleInfo><name type="personal"><namePart type="given">Long‐Li</namePart><namePart type="family">Lai</namePart><affiliation>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</affiliation><affiliation>Current Address: Institute of Chemistry, Academia Sinica, Nankang, Taipei, 11529 Republic of China</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">David H.</namePart><namePart type="family">Reid</namePart><affiliation>Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</affiliation><description>Correspondence: Department of Chemistry, University of the Witwatersrand, Johannesburg, South Africa</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Sue‐Lein</namePart><namePart type="family">Wang</namePart><affiliation>Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Fen‐Ling</namePart><namePart type="family">Liao</namePart><affiliation>Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan 30043, Republic of China</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>VCH Publishers, Inc.</publisher><place><placeTerm type="text">Florida</placeTerm></place><dateIssued encoding="w3cdtf">1994-09</dateIssued><dateCaptured encoding="w3cdtf">1994-07-29</dateCaptured><copyrightDate encoding="w3cdtf">1994</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">1</extent><extent unit="tables">8</extent><extent unit="references">14</extent></physicalDescription><abstract lang="en">Four thiophene derivatives have been obtained unexpectedly from the reaction of N‐phenylacetyithiobenzamides with P4S10 in boiling carbon disulfide. The structure of one of these was established by X‐ray crystallography.</abstract><note type="content">*Studies of Heterocyclic Compounds, Part 33.</note><relatedItem type="host"><titleInfo><title>Heteroatom Chemistry</title></titleInfo><titleInfo type="abbreviated"><title>Heteroatom Chem.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Article</topic></subject><identifier type="ISSN">1042-7163</identifier><identifier type="eISSN">1098-1071</identifier><identifier type="DOI">10.1002/(ISSN)1098-1071</identifier><identifier type="PublisherID">HC</identifier><part><date>1994</date><detail type="volume"><caption>vol.</caption><number>5</number></detail><detail type="issue"><caption>no.</caption><number>5‐6</number></detail><extent unit="pages"><start>479</start><end>486</end><total>8</total></extent></part></relatedItem><identifier type="istex">D3913F19A10D496B57DEDDA034EEEF140056AEDC</identifier><identifier type="DOI">10.1002/hc.520050510</identifier><identifier type="ArticleID">HC520050510</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1994 VCH Publishers, Inc.</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>VCH Publishers, Inc.</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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