A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.
Identifieur interne : 001469 ( Istex/Corpus ); précédent : 001468; suivant : 001470A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.
Auteurs : Shatrughan P. Shahi ; Kazunori KoideSource :
- ChemInform [ 0931-7597 ] ; 2004-08-24.
English descriptors
- KwdEn :
- Acetylides, Aldehyde, Aldehydes alkyl propiolates, Alkyl, Alkyne, Angew, Base title compounds tions, Carboxylic, Chem, Condiin, Conventional conditions, Ester, Esters hydroxycarboxylic acids, Ether, Ether carboxylic acids, Hydroxycarboxylic, Hydroxycarboxylic acids, Ketone, Ketones withunder, Koide, Mild method, Powerful method, Propiolates, Reactive, Reactive species, Shahi, Silver acetylides, Tions, Univ, Withunder.
- Teeft :
- Acetylides, Aldehyde, Aldehydes alkyl propiolates, Alkyl, Alkyne, Angew, Base title compounds tions, Carboxylic, Chem, Condiin, Conventional conditions, Ester, Esters hydroxycarboxylic acids, Ether, Ether carboxylic acids, Hydroxycarboxylic, Hydroxycarboxylic acids, Ketone, Ketones withunder, Koide, Mild method, Powerful method, Propiolates, Reactive, Reactive species, Shahi, Silver acetylides, Tions, Univ, Withunder.
Abstract
For Abstract see ChemInform Abstract in Full Text.
Url:
DOI: 10.1002/chin.200434088
Links to Exploration step
ISTEX:59CC4241E6756029A45765460DB683034CA726F1Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
<author><name sortKey="Shahi, Shatrughan P" sort="Shahi, Shatrughan P" uniqKey="Shahi S" first="Shatrughan P." last="Shahi">Shatrughan P. Shahi</name>
<affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Koide, Kazunori" sort="Koide, Kazunori" uniqKey="Koide K" first="Kazunori" last="Koide">Kazunori Koide</name>
<affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</mods:affiliation>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:59CC4241E6756029A45765460DB683034CA726F1</idno>
<date when="2004" year="2004">2004</date>
<idno type="doi">10.1002/chin.200434088</idno>
<idno type="url">https://api.istex.fr/document/59CC4241E6756029A45765460DB683034CA726F1/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001469</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001469</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
<author><name sortKey="Shahi, Shatrughan P" sort="Shahi, Shatrughan P" uniqKey="Shahi S" first="Shatrughan P." last="Shahi">Shatrughan P. Shahi</name>
<affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</mods:affiliation>
</affiliation>
</author>
<author><name sortKey="Koide, Kazunori" sort="Koide, Kazunori" uniqKey="Koide K" first="Kazunori" last="Koide">Kazunori Koide</name>
<affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</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">35</biblScope>
<biblScope unit="issue">34</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="2004-08-24">2004-08-24</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>Acetylides</term>
<term>Aldehyde</term>
<term>Aldehydes alkyl propiolates</term>
<term>Alkyl</term>
<term>Alkyne</term>
<term>Angew</term>
<term>Base title compounds tions</term>
<term>Carboxylic</term>
<term>Chem</term>
<term>Condiin</term>
<term>Conventional conditions</term>
<term>Ester</term>
<term>Esters hydroxycarboxylic acids</term>
<term>Ether</term>
<term>Ether carboxylic acids</term>
<term>Hydroxycarboxylic</term>
<term>Hydroxycarboxylic acids</term>
<term>Ketone</term>
<term>Ketones withunder</term>
<term>Koide</term>
<term>Mild method</term>
<term>Powerful method</term>
<term>Propiolates</term>
<term>Reactive</term>
<term>Reactive species</term>
<term>Shahi</term>
<term>Silver acetylides</term>
<term>Tions</term>
<term>Univ</term>
<term>Withunder</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Acetylides</term>
<term>Aldehyde</term>
<term>Aldehydes alkyl propiolates</term>
<term>Alkyl</term>
<term>Alkyne</term>
<term>Angew</term>
<term>Base title compounds tions</term>
<term>Carboxylic</term>
<term>Chem</term>
<term>Condiin</term>
<term>Conventional conditions</term>
<term>Ester</term>
<term>Esters hydroxycarboxylic acids</term>
<term>Ether</term>
<term>Ether carboxylic acids</term>
<term>Hydroxycarboxylic</term>
<term>Hydroxycarboxylic acids</term>
<term>Ketone</term>
<term>Ketones withunder</term>
<term>Koide</term>
<term>Mild method</term>
<term>Powerful method</term>
<term>Propiolates</term>
<term>Reactive</term>
<term>Reactive species</term>
<term>Shahi</term>
<term>Silver acetylides</term>
<term>Tions</term>
<term>Univ</term>
<term>Withunder</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">For Abstract see ChemInform Abstract in Full Text.</div>
</front>
</TEI>
<istex><corpusName>wiley</corpusName>
<keywords><teeft><json:string>ester</json:string>
<json:string>hydroxycarboxylic</json:string>
<json:string>chem</json:string>
<json:string>carboxylic</json:string>
<json:string>ether carboxylic acids</json:string>
<json:string>aldehyde</json:string>
<json:string>ketone</json:string>
<json:string>alkyne</json:string>
<json:string>univ</json:string>
<json:string>alkyl</json:string>
<json:string>propiolates</json:string>
<json:string>aldehydes alkyl propiolates</json:string>
<json:string>esters hydroxycarboxylic acids</json:string>
<json:string>withunder</json:string>
<json:string>ketones withunder</json:string>
<json:string>hydroxycarboxylic acids</json:string>
<json:string>tions</json:string>
<json:string>base title compounds tions</json:string>
<json:string>conventional conditions</json:string>
<json:string>acetylides</json:string>
<json:string>silver acetylides</json:string>
<json:string>mild method</json:string>
<json:string>powerful method</json:string>
<json:string>reactive</json:string>
<json:string>reactive species</json:string>
<json:string>shahi</json:string>
<json:string>koide</json:string>
<json:string>angew</json:string>
<json:string>condiin</json:string>
<json:string>ether</json:string>
</teeft>
</keywords>
<author><json:item><name>Shatrughan P. Shahi</name>
<affiliations><json:string>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</json:string>
</affiliations>
</json:item>
<json:item><name>Kazunori Koide</name>
<affiliations><json:string>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</json:string>
</affiliations>
</json:item>
</author>
<subject><json:item><lang><json:string>eng</json:string>
</lang>
<value>hydroxycarboxylic acids (ether carboxylic acids) and esters (benzene compounds)</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>reactions of organo‐metal compounds</value>
</json:item>
<json:item><lang><json:string>eng</json:string>
</lang>
<value>amino acids, peptides</value>
</json:item>
</subject>
<articleId><json:string>CHIN200434088</json:string>
</articleId>
<arkIstex>ark:/67375/WNG-Q1PL7HL0-D</arkIstex>
<language><json:string>eng</json:string>
</language>
<originalGenre><json:string>article</json:string>
</originalGenre>
<abstract>For Abstract see ChemInform Abstract in Full Text.</abstract>
<qualityIndicators><score>2.21</score>
<pdfWordCount>114</pdfWordCount>
<pdfCharCount>727</pdfCharCount>
<pdfVersion>1.3</pdfVersion>
<pdfPageCount>1</pdfPageCount>
<pdfPageSize>416 x 589 pts</pdfPageSize>
<refBibsNative>true</refBibsNative>
<abstractWordCount>8</abstractWordCount>
<abstractCharCount>50</abstractCharCount>
<keywordCount>4</keywordCount>
</qualityIndicators>
<title>A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic 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>35</volume>
<issue>34</issue>
<genre><json:string>journal</json:string>
</genre>
<subject><json:item><value>Isocyclic Compounds</value>
</json:item>
</subject>
</host>
<namedEntities><unitex><date><json:string>2004</json:string>
</date>
<geogName></geogName>
<orgName></orgName>
<orgName_funder></orgName_funder>
<orgName_provider></orgName_provider>
<persName></persName>
<placeName><json:string>Pittsburgh</json:string>
<json:string>PA</json:string>
</placeName>
<ref_url></ref_url>
<ref_bibl></ref_bibl>
<bibl></bibl>
</unitex>
</namedEntities>
<ark><json:string>ark:/67375/WNG-Q1PL7HL0-D</json:string>
</ark>
<categories><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string>
<json:string>2 - sciences exactes et technologie</json:string>
<json:string>3 - terre, ocean, espace</json:string>
<json:string>4 - geophysique externe</json:string>
</inist>
</categories>
<publicationDate>2004</publicationDate>
<copyrightDate>2004</copyrightDate>
<doi><json:string>10.1002/chin.200434088</json:string>
</doi>
<id>59CC4241E6756029A45765460DB683034CA726F1</id>
<score>1</score>
<fulltext><json:item><extension>pdf</extension>
<original>true</original>
<mimetype>application/pdf</mimetype>
<uri>https://api.istex.fr/document/59CC4241E6756029A45765460DB683034CA726F1/fulltext/pdf</uri>
</json:item>
<json:item><extension>zip</extension>
<original>false</original>
<mimetype>application/zip</mimetype>
<uri>https://api.istex.fr/document/59CC4241E6756029A45765460DB683034CA726F1/fulltext/zip</uri>
</json:item>
<istex:fulltextTEI uri="https://api.istex.fr/document/59CC4241E6756029A45765460DB683034CA726F1/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
</titleStmt>
<publicationStmt><authority>ISTEX</authority>
<publisher>WILEY‐VCH Verlag</publisher>
<pubPlace>Weinheim</pubPlace>
<availability><licence>Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</licence>
</availability>
<date type="published" when="2004-08-24"></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">A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
<author xml:id="author-0000"><persName><forename type="first">Shatrughan P.</forename>
<surname>Shahi</surname>
</persName>
<affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA<address><country key="US"></country>
</address>
</affiliation>
</author>
<author xml:id="author-0001"><persName><forename type="first">Kazunori</forename>
<surname>Koide</surname>
</persName>
<affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA<address><country key="US"></country>
</address>
</affiliation>
</author>
<idno type="istex">59CC4241E6756029A45765460DB683034CA726F1</idno>
<idno type="ark">ark:/67375/WNG-Q1PL7HL0-D</idno>
<idno type="DOI">10.1002/chin.200434088</idno>
<idno type="unit">CHIN200434088</idno>
<idno type="toTypesetVersion">file:CHIN.CHIN200434088.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.v35:34</idno>
<idno type="product">CHIN</idno>
<imprint><biblScope unit="vol">35</biblScope>
<biblScope unit="issue">34</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="2004-08-24"></date>
</imprint>
</monogr>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head>
<p>For Abstract see ChemInform Abstract in Full Text.</p>
</abstract>
<textClass><keywords xml:lang="en"><term xml:id="kwd1">hydroxycarboxylic acids (ether carboxylic acids) and esters (benzene compounds)</term>
<term xml:id="kwd2">hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters</term>
<term xml:id="kwd3">reactions of organo‐metal compounds</term>
<term xml:id="kwd4">amino acids, peptides</term>
</keywords>
<keywords rend="articleCategory"><term>Isocyclic Compounds</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/59CC4241E6756029A45765460DB683034CA726F1/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="340"><doi origin="wiley" registered="yes">10.1002/chin.v35:34</doi>
<numberingGroup><numbering type="journalVolume" number="35">35</numbering>
<numbering type="journalIssue">34</numbering>
</numberingGroup>
<coverDate startDate="2004-08-24">August 24, 2004</coverDate>
</publicationMeta>
<publicationMeta level="unit" type="article" position="88" status="forIssue"><doi origin="wiley" registered="yes">10.1002/chin.200434088</doi>
<idGroup><id type="unit" value="CHIN200434088"></id>
</idGroup>
<countGroup><count type="pageTotal" number="1"></count>
</countGroup>
<titleGroup><title type="articleCategory">Isocyclic Compounds</title>
</titleGroup>
<copyright ownership="publisher">Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</copyright>
<eventGroup><event type="firstOnline" date="2004-08-02"></event>
<event type="publishedOnlineFinalForm" date="2004-08-02"></event>
<event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-15"></event>
<event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-14"></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.CHIN200434088.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">A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
</titleGroup>
<creators><creator xml:id="au1" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Shatrughan P.</givenNames>
<familyName>Shahi</familyName>
</personName>
</creator>
<creator xml:id="au2" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Kazunori</givenNames>
<familyName>Koide</familyName>
</personName>
</creator>
</creators>
<affiliationGroup><affiliation xml:id="a1" countryCode="US" type="organization"><unparsedAffiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</unparsedAffiliation>
</affiliation>
</affiliationGroup>
<keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">hydroxycarboxylic acids (ether carboxylic acids) and esters (benzene compounds)</keyword>
<keyword xml:id="kwd2">hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters</keyword>
<keyword xml:id="kwd3">reactions of organo‐metal compounds</keyword>
<keyword xml:id="kwd4">amino acids, peptides</keyword>
</keywordGroup>
<abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title>
<p>For Abstract see ChemInform Abstract in Full Text.</p>
</abstract>
</abstractGroup>
</contentMeta>
</header>
</component>
</istex:document>
</istex:metadataXml>
<mods version="3.6"><titleInfo lang="en"><title>A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
</titleInfo>
<titleInfo type="alternative" contentType="CDATA" lang="en"><title>A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters.</title>
</titleInfo>
<name type="personal"><namePart type="given">Shatrughan P.</namePart>
<namePart type="family">Shahi</namePart>
<affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</affiliation>
<role><roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal"><namePart type="given">Kazunori</namePart>
<namePart type="family">Koide</namePart>
<affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</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">2004-08-24</dateIssued>
<copyrightDate encoding="w3cdtf">2004</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">For Abstract see ChemInform Abstract in Full Text.</abstract>
<subject lang="en"><genre>keywords</genre>
<topic>hydroxycarboxylic acids (ether carboxylic acids) and esters (benzene compounds)</topic>
<topic>hydroxycarboxylic acids (ether carboxylic acids) (acyclic compounds) and esters</topic>
<topic>reactions of organo‐metal compounds</topic>
<topic>amino acids, peptides</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>Isocyclic Compounds</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>2004</date>
<detail type="volume"><caption>vol.</caption>
<number>35</number>
</detail>
<detail type="issue"><caption>no.</caption>
<number>34</number>
</detail>
<extent unit="pages"><total>1</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">59CC4241E6756029A45765460DB683034CA726F1</identifier>
<identifier type="ark">ark:/67375/WNG-Q1PL7HL0-D</identifier>
<identifier type="DOI">10.1002/chin.200434088</identifier>
<identifier type="ArticleID">CHIN200434088</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 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/59CC4241E6756029A45765460DB683034CA726F1/metadata/json</uri>
</json:item>
</metadata>
<serie></serie>
</istex>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Amérique/explor/PittsburghV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001469 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 001469 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Amérique |area= PittsburghV1 |flux= Istex |étape= Corpus |type= RBID |clé= ISTEX:59CC4241E6756029A45765460DB683034CA726F1 |texte= A Mild Method for the Preparation of γ‐Hydroxy‐α,β‐acetylenic Esters. }}
![]() | This area was generated with Dilib version V0.6.38. | ![]() |