The NiCl2‐Li‐Arene (cat.) Combination as Reducing System, Part 9: Catalytic Hydrogenation of Organic Compounds using the NiCl2‐Li‐(Naphthalene or Polymer‐Supported Naphthalene) (cat.) Combination
Identifieur interne : 000509 ( Main/Exploration ); précédent : 000508; suivant : 000510The NiCl2‐Li‐Arene (cat.) Combination as Reducing System, Part 9: Catalytic Hydrogenation of Organic Compounds using the NiCl2‐Li‐(Naphthalene or Polymer‐Supported Naphthalene) (cat.) Combination
Auteurs : Francisco Alonso ; Pablo Candela ; Cecilia G Mez ; Miguel Yus [Espagne]Source :
- Advanced Synthesis & Catalysis [ 1615-4150 ] ; 2003-01.
English descriptors
Abstract
The reaction of lithium powder, a catalytic amount of naphthalene or polymer‐supported naphthalene, and anhydrous nickel(II) chloride, in THF at room temperature, generates a finely divided and very reactive nickel(0) which has been efficiently applied to the catalytic hydrogenation of different organic compounds such as alkenes, alkynes, carbonyl compounds, imines, organic halides, aromatic compounds, hydrazines, azoxy compounds, and N‐oxides.
Url:
DOI: 10.1002/adsc.200390022
Affiliations:
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Combination</title><author><name sortKey="Alonso, Francisco" sort="Alonso, Francisco" uniqKey="Alonso F" first="Francisco" last="Alonso">Francisco Alonso</name></author><author><name sortKey="Candela, Pablo" sort="Candela, Pablo" uniqKey="Candela P" first="Pablo" last="Candela">Pablo Candela</name></author><author><name sortKey="G Mez, Cecilia" sort="G Mez, Cecilia" uniqKey="G Mez C" first="Cecilia" last="G Mez">Cecilia G Mez</name></author><author><name sortKey="Yus, Miguel" sort="Yus, Miguel" uniqKey="Yus M" first="Miguel" last="Yus">Miguel Yus</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:86751AC1E61BB69FB01BE0AF60EECECE6AB342B7</idno><date when="2003" year="2003">2003</date><idno type="doi">10.1002/adsc.200390022</idno><idno type="url">https://api.istex.fr/document/86751AC1E61BB69FB01BE0AF60EECECE6AB342B7/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000842</idno><idno type="wicri:Area/Istex/Curation">000761</idno><idno type="wicri:Area/Istex/Checkpoint">000477</idno><idno type="wicri:doubleKey">1615-4150:2003:Alonso F:the:nicl:li</idno><idno type="wicri:Area/Main/Merge">000537</idno><idno type="wicri:Area/Main/Curation">000531</idno><idno type="wicri:Area/Main/Exploration">000509</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The NiCl2‐Li‐Arene (cat.) Combination as Reducing System, Part 9: Catalytic Hydrogenation of Organic Compounds using the NiCl2‐Li‐(Naphthalene or Polymer‐Supported Naphthalene) (cat.) Combination</title><author><name sortKey="Alonso, Francisco" sort="Alonso, Francisco" uniqKey="Alonso F" first="Francisco" last="Alonso">Francisco Alonso</name><affiliation><wicri:noCountry code="subField">Spain Fax: (+34)‐965 903549</wicri:noCountry></affiliation></author><author><name sortKey="Candela, Pablo" sort="Candela, Pablo" uniqKey="Candela P" first="Pablo" last="Candela">Pablo Candela</name><affiliation><wicri:noCountry code="subField">Spain Fax: (+34)‐965 903549</wicri:noCountry></affiliation></author><author><name sortKey="G Mez, Cecilia" sort="G Mez, Cecilia" uniqKey="G Mez C" first="Cecilia" last="G Mez">Cecilia G Mez</name><affiliation><wicri:noCountry code="subField">Spain Fax: (+34)‐965 903549</wicri:noCountry></affiliation></author><author><name sortKey="Yus, Miguel" sort="Yus, Miguel" uniqKey="Yus M" first="Miguel" last="Yus">Miguel Yus</name><affiliation><wicri:noCountry code="subField">Spain Fax: (+34)‐965 903549</wicri:noCountry></affiliation><affiliation wicri:level="1"><country wicri:rule="url">Espagne</country></affiliation></author></analytic><monogr></monogr><series><title level="j">Advanced Synthesis & Catalysis</title><title level="j" type="abbrev">Adv. Synth. Catal.</title><idno type="ISSN">1615-4150</idno><idno type="eISSN">1615-4169</idno><imprint><publisher>WILEY‐VCH Verlag</publisher><pubPlace>Weinheim</pubPlace><date type="published" when="2003-01">2003-01</date><biblScope unit="volume">345</biblScope><biblScope unit="issue">1‐2</biblScope><biblScope unit="page" from="275">275</biblScope><biblScope unit="page" to="279">279</biblScope></imprint><idno type="ISSN">1615-4150</idno></series><idno type="istex">86751AC1E61BB69FB01BE0AF60EECECE6AB342B7</idno><idno type="DOI">10.1002/adsc.200390022</idno><idno type="ArticleID">ADSC200390022</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1615-4150</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>catalytic hydrogenation</term><term>lithium</term><term>naphthalene</term><term>nickel</term><term>polymer‐supported naphthalene</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The reaction of lithium powder, a catalytic amount of naphthalene or polymer‐supported naphthalene, and anhydrous nickel(II) chloride, in THF at room temperature, generates a finely divided and very reactive nickel(0) which has been efficiently applied to the catalytic hydrogenation of different organic compounds such as alkenes, alkynes, carbonyl compounds, imines, organic halides, aromatic compounds, hydrazines, azoxy compounds, and N‐oxides.</div></front></TEI><affiliations><list><country><li>Espagne</li></country></list><tree><noCountry><name sortKey="Alonso, Francisco" sort="Alonso, Francisco" uniqKey="Alonso F" first="Francisco" last="Alonso">Francisco Alonso</name><name sortKey="Candela, Pablo" sort="Candela, Pablo" uniqKey="Candela P" first="Pablo" last="Candela">Pablo Candela</name><name sortKey="G Mez, Cecilia" sort="G Mez, Cecilia" uniqKey="G Mez C" first="Cecilia" last="G Mez">Cecilia G Mez</name></noCountry><country name="Espagne"><noRegion><name sortKey="Yus, Miguel" sort="Yus, Miguel" uniqKey="Yus M" first="Miguel" last="Yus">Miguel Yus</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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