ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.
Identifieur interne : 002315 ( Istex/Corpus ); précédent : 002314; suivant : 002316ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.
Auteurs : Tsuyoshi Taniguchi ; Dennis P. CurranSource :
- ChemInform [ 0931-7597 ] ; 2012-12-25.
English descriptors
- KwdEn :
- Aldehyde, Aldehyde group, Ambient, Ambient conditions, Borane, Boranes, Boron hydrides, Carbene, Carbene borane, Carbene boranes, Chem, Cheminform, Curran, Dimethyl, Dimethyl analogue, Gmbh, Keto, Keto group, Ketone, Kgaa, Klein cheminform, Lett, Rapid reduction, Secondary alcohols, Sio2, Taniguchi, Univ, Verlag, Verlag gmbh, Weinheim, Weinheim cheminform.
- Teeft :
- Aldehyde, Aldehyde group, Ambient, Ambient conditions, Borane, Boranes, Boron hydrides, Carbene, Carbene borane, Carbene boranes, Chem, Cheminform, Curran, Dimethyl, Dimethyl analogue, Gmbh, Keto, Keto group, Ketone, Kgaa, Klein cheminform, Lett, Rapid reduction, Secondary alcohols, Sio2, Taniguchi, Univ, Verlag, Verlag gmbh, Weinheim, Weinheim cheminform.
Abstract
One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO2, which is crucial for the rapid reduction.
Url:
DOI: 10.1002/chin.201252072
Links to Exploration step
ISTEX:958D9C4B9DE372B0DB9282206930ACDD0E3F0F42Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title><author><name sortKey="Taniguchi, Tsuyoshi" sort="Taniguchi, Tsuyoshi" uniqKey="Taniguchi T" first="Tsuyoshi" last="Taniguchi">Tsuyoshi Taniguchi</name><affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</mods:affiliation></affiliation></author><author><name sortKey="Curran, Dennis P" sort="Curran, Dennis P" uniqKey="Curran D" first="Dennis P." last="Curran">Dennis P. Curran</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:958D9C4B9DE372B0DB9282206930ACDD0E3F0F42</idno><date when="2012" year="2012">2012</date><idno type="doi">10.1002/chin.201252072</idno><idno type="url">https://api.istex.fr/document/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002315</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">002315</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title><author><name sortKey="Taniguchi, Tsuyoshi" sort="Taniguchi, Tsuyoshi" uniqKey="Taniguchi T" first="Tsuyoshi" last="Taniguchi">Tsuyoshi Taniguchi</name><affiliation><mods:affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</mods:affiliation></affiliation></author><author><name sortKey="Curran, Dennis P" sort="Curran, Dennis P" uniqKey="Curran D" first="Dennis P." last="Curran">Dennis P. Curran</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">43</biblScope><biblScope unit="issue">52</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="2012-12-25">2012-12-25</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>Aldehyde</term><term>Aldehyde group</term><term>Ambient</term><term>Ambient conditions</term><term>Borane</term><term>Boranes</term><term>Boron hydrides</term><term>Carbene</term><term>Carbene borane</term><term>Carbene boranes</term><term>Chem</term><term>Cheminform</term><term>Curran</term><term>Dimethyl</term><term>Dimethyl analogue</term><term>Gmbh</term><term>Keto</term><term>Keto group</term><term>Ketone</term><term>Kgaa</term><term>Klein cheminform</term><term>Lett</term><term>Rapid reduction</term><term>Secondary alcohols</term><term>Sio2</term><term>Taniguchi</term><term>Univ</term><term>Verlag</term><term>Verlag gmbh</term><term>Weinheim</term><term>Weinheim cheminform</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Aldehyde</term><term>Aldehyde group</term><term>Ambient</term><term>Ambient conditions</term><term>Borane</term><term>Boranes</term><term>Boron hydrides</term><term>Carbene</term><term>Carbene borane</term><term>Carbene boranes</term><term>Chem</term><term>Cheminform</term><term>Curran</term><term>Dimethyl</term><term>Dimethyl analogue</term><term>Gmbh</term><term>Keto</term><term>Keto group</term><term>Ketone</term><term>Kgaa</term><term>Klein cheminform</term><term>Lett</term><term>Rapid reduction</term><term>Secondary alcohols</term><term>Sio2</term><term>Taniguchi</term><term>Univ</term><term>Verlag</term><term>Verlag gmbh</term><term>Weinheim</term><term>Weinheim cheminform</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO2, which is crucial for the rapid reduction.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>aldehyde</json:string><json:string>carbene</json:string><json:string>ketone</json:string><json:string>cheminform</json:string><json:string>verlag</json:string><json:string>gmbh</json:string><json:string>verlag gmbh</json:string><json:string>kgaa</json:string><json:string>weinheim</json:string><json:string>dimethyl analogue</json:string><json:string>secondary alcohols</json:string><json:string>ambient</json:string><json:string>ambient conditions</json:string><json:string>sio2</json:string><json:string>rapid reduction</json:string><json:string>weinheim cheminform</json:string><json:string>keto</json:string><json:string>keto group</json:string><json:string>taniguchi</json:string><json:string>curran</json:string><json:string>lett</json:string><json:string>chem</json:string><json:string>univ</json:string><json:string>boranes</json:string><json:string>klein cheminform</json:string><json:string>carbene boranes</json:string><json:string>boron hydrides</json:string><json:string>borane</json:string><json:string>carbene borane</json:string><json:string>dimethyl</json:string><json:string>aldehyde group</json:string></teeft></keywords><author><json:item><name>Tsuyoshi Taniguchi</name><affiliations><json:string>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA</json:string></affiliations></json:item><json:item><name>Dennis P. Curran</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>alcohols (benzene compounds)</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>reduction, hydrogenation</value></json:item></subject><articleId><json:string>CHIN201252072</json:string></articleId><arkIstex>ark:/67375/WNG-2574C9TL-1</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO2, which is crucial for the rapid reduction.</abstract><qualityIndicators><score>2.684</score><pdfWordCount>120</pdfWordCount><pdfCharCount>702</pdfCharCount><pdfVersion>1.5</pdfVersion><pdfPageCount>2</pdfPageCount><pdfPageSize>417 x 590 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>47</abstractWordCount><abstractCharCount>275</abstractCharCount><keywordCount>2</keywordCount></qualityIndicators><title>ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</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>43</volume><issue>52</issue><genre><json:string>journal</json:string></genre><subject><json:item><value>Isocyclic Compounds</value></json:item></subject></host><namedEntities><unitex><date><json:string>2012</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><json:string>http://dx.doi.org/</json:string></ref_url><ref_bibl></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-2574C9TL-1</json:string></ark><categories><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences medicales</json:string><json:string>4 - chirurgie (generalites). transplantations, greffes d'organes et de tissus. pathologie des greffons</json:string></inist></categories><publicationDate>2012</publicationDate><copyrightDate>2012</copyrightDate><doi><json:string>10.1002/chin.201252072</json:string></doi><id>958D9C4B9DE372B0DB9282206930ACDD0E3F0F42</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><availability><licence>Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</licence></availability><date type="published" when="2012-12-25"></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: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title><author xml:id="author-0000"><persName><forename type="first">Tsuyoshi</forename><surname>Taniguchi</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">Dennis P.</forename><surname>Curran</surname></persName><affiliation>Dep. Chem., Univ. Pittsburgh, Pittsburgh, PA 15260, USA<address><country key="US"></country></address></affiliation></author><idno type="istex">958D9C4B9DE372B0DB9282206930ACDD0E3F0F42</idno><idno type="ark">ark:/67375/WNG-2574C9TL-1</idno><idno type="DOI">10.1002/chin.201252072</idno><idno type="unit">CHIN201252072</idno><idno type="toTypesetVersion">file:CHIN.CHIN201252072.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.v43.52</idno><idno type="product">CHIN</idno><imprint><biblScope unit="vol">43</biblScope><biblScope unit="issue">52</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="2012-12-25"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO<hi rend="subscript">2</hi>, which is crucial for the rapid reduction.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">alcohols (benzene compounds)</term><term xml:id="kwd2">reduction, hydrogenation</term></keywords><keywords rend="articleCategory"><term>Isocyclic Compounds</term></keywords><keywords rend="tocHeading1"><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/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/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="520"><doi origin="wiley" registered="yes">10.1002/chin.v43.52</doi><numberingGroup><numbering type="journalVolume" number="43">43</numbering><numbering type="journalIssue">52</numbering></numberingGroup><coverDate startDate="2012-12-25">December 25, 2012</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="74" status="forIssue"><doi origin="wiley" registered="yes">10.1002/chin.201252072</doi><idGroup><id type="unit" value="CHIN201252072"></id></idGroup><countGroup><count type="pageTotal" number="1"></count></countGroup><titleGroup><title type="articleCategory">Isocyclic Compounds</title><title type="tocHeading1">Isocyclic Compounds</title></titleGroup><copyright ownership="publisher">Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</copyright><eventGroup><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:3.1.9 mode:FullText" date="2013-01-09"></event><event type="publishedOnlineFinalForm" date="2012-12-18"></event><event type="firstOnline" date="2012-12-18"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-13"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.3.4 mode:FullText" date="2015-02-24"></event></eventGroup><numberingGroup><numbering type="pageFirst">no</numbering><numbering type="pageLast">no</numbering></numberingGroup><linkGroup><link type="toTypesetVersion" href="file:CHIN.CHIN201252072.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: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Tsuyoshi</givenNames><familyName>Taniguchi</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#a1"><personName><givenNames>Dennis P.</givenNames><familyName>Curran</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">alcohols (benzene compounds)</keyword><keyword xml:id="kwd2">reduction, hydrogenation</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO<sub>2</sub>, which is crucial for the rapid reduction.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.</title></titleInfo><name type="personal"><namePart type="given">Tsuyoshi</namePart><namePart type="family">Taniguchi</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">Dennis P.</namePart><namePart type="family">Curran</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">2012-12-25</dateIssued><copyrightDate encoding="w3cdtf">2012</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">One, two, or all three of the boron hydrides of carbene borane NHC and its dimethyl analogue can be transferred to the aldehydes and ketones to give primary and secondary alcohols under ambient conditions and in the presence of SiO2, which is crucial for the rapid reduction.</abstract><subject lang="en"><genre>keywords</genre><topic>alcohols (benzene compounds)</topic><topic>reduction, hydrogenation</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>2012</date><detail type="volume"><caption>vol.</caption><number>43</number></detail><detail type="issue"><caption>no.</caption><number>52</number></detail><extent unit="pages"><total>1</total></extent></part></relatedItem><identifier type="istex">958D9C4B9DE372B0DB9282206930ACDD0E3F0F42</identifier><identifier type="ark">ark:/67375/WNG-2574C9TL-1</identifier><identifier type="DOI">10.1002/chin.201252072</identifier><identifier type="ArticleID">CHIN201252072</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2012 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/958D9C4B9DE372B0DB9282206930ACDD0E3F0F42/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 002315 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 002315 | 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:958D9C4B9DE372B0DB9282206930ACDD0E3F0F42
|texte= ChemInform Abstract: Silica Gel Promotes Reductions of Aldehydes and Ketones by N‐Heterocyclic Carbene Boranes.
}}
| This area was generated with Dilib version V0.6.38. |  |