ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.
Identifieur interne : 005B27 ( Istex/Curation ); précédent : 005B26; suivant : 005B28ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.
Auteurs : Ken Yamashita [Japon] ; Yoshihiko Yamamoto [Japon] ; Hisao Nishiyama [Japon]Source :
- ChemInform [ 0931-7597 ] ; 2012-09-25.
English descriptors
- KwdEn :
- Alkyl, Bicyclic, Bicyclic furan skeletons, Bicyclic furans, Broad spectrum, Chem, Cheminform, Chikusa, Cyclization, Diynes, Dmso, Edented, Furan, Furan derivatives, Furan oxygen, Gmbh, Kgaa, Lindner, Lindner cheminform, Nagoya, Nagoya univ, Nishiyama, Oligoaryl, Optimized, Optimized conditions dmso, Oxygenative, Pharm, Ruthenacycle, Ruthenacyclopentatriene, Substituents, Terminal alkyl substituents, Terminal aryl substituents, Transfer oxygenative cyclization, Univ, Verlag, Verlag gmbh, Weinheim, Weinheim cheminform, Yamamoto, Yamashita.
- Teeft :
- Alkyl, Bicyclic, Bicyclic furan skeletons, Bicyclic furans, Broad spectrum, Chem, Cheminform, Chikusa, Cyclization, Diynes, Dmso, Edented, Furan, Furan derivatives, Furan oxygen, Gmbh, Kgaa, Lindner, Lindner cheminform, Nagoya, Nagoya univ, Nishiyama, Oligoaryl, Optimized, Optimized conditions dmso, Oxygenative, Pharm, Ruthenacycle, Ruthenacyclopentatriene, Substituents, Terminal alkyl substituents, Terminal aryl substituents, Transfer oxygenative cyclization, Univ, Verlag, Verlag gmbh, Weinheim, Weinheim cheminform, Yamamoto, Yamashita.
Abstract
Generally, a broad spectrum of bicyclic furan skeletons can be obtained from diynes bearing 2 terminal aryl substituents under the optimized conditions A)‐C).
Url:
DOI: 10.1002/chin.201239103
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: Pour aller vers cette notice dans l'étape Curation :005B27
Links to Exploration step
ISTEX:B727252C6C8053759EF768BA72D72C739385037ALe document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.</title>
<author><name sortKey="Yamashita, Ken" sort="Yamashita, Ken" uniqKey="Yamashita K" first="Ken" last="Yamashita">Ken Yamashita</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</affiliation>
</author>
<author><name sortKey="Yamamoto, Yoshihiko" sort="Yamamoto, Yoshihiko" uniqKey="Yamamoto Y" first="Yoshihiko" last="Yamamoto">Yoshihiko Yamamoto</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</affiliation>
</author>
<author><name sortKey="Nishiyama, Hisao" sort="Nishiyama, Hisao" uniqKey="Nishiyama H" first="Hisao" last="Nishiyama">Hisao Nishiyama</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:B727252C6C8053759EF768BA72D72C739385037A</idno>
<date when="2012" year="2012">2012</date>
<idno type="doi">10.1002/chin.201239103</idno>
<idno type="url">https://api.istex.fr/document/B727252C6C8053759EF768BA72D72C739385037A/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">005B27</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">005B27</idno>
<idno type="wicri:Area/Istex/Curation">005B27</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.</title>
<author><name sortKey="Yamashita, Ken" sort="Yamashita, Ken" uniqKey="Yamashita K" first="Ken" last="Yamashita">Ken Yamashita</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</affiliation>
</author>
<author><name sortKey="Yamamoto, Yoshihiko" sort="Yamamoto, Yoshihiko" uniqKey="Yamamoto Y" first="Yoshihiko" last="Yamamoto">Yoshihiko Yamamoto</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</affiliation>
</author>
<author><name sortKey="Nishiyama, Hisao" sort="Nishiyama, Hisao" uniqKey="Nishiyama H" first="Hisao" last="Nishiyama">Hisao Nishiyama</name>
<affiliation wicri:level="1"><mods:affiliation>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464, Japan</mods:affiliation>
<country xml:lang="fr">Japon</country>
<wicri:regionArea>Dep. Basic Med. Sci., Grad. Sch. Pharm. Sci., Nagoya Univ., Chikusa, Nagoya 464</wicri:regionArea>
</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">39</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="2012-09-25">2012-09-25</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>Alkyl</term>
<term>Bicyclic</term>
<term>Bicyclic furan skeletons</term>
<term>Bicyclic furans</term>
<term>Broad spectrum</term>
<term>Chem</term>
<term>Cheminform</term>
<term>Chikusa</term>
<term>Cyclization</term>
<term>Diynes</term>
<term>Dmso</term>
<term>Edented</term>
<term>Furan</term>
<term>Furan derivatives</term>
<term>Furan oxygen</term>
<term>Gmbh</term>
<term>Kgaa</term>
<term>Lindner</term>
<term>Lindner cheminform</term>
<term>Nagoya</term>
<term>Nagoya univ</term>
<term>Nishiyama</term>
<term>Oligoaryl</term>
<term>Optimized</term>
<term>Optimized conditions dmso</term>
<term>Oxygenative</term>
<term>Pharm</term>
<term>Ruthenacycle</term>
<term>Ruthenacyclopentatriene</term>
<term>Substituents</term>
<term>Terminal alkyl substituents</term>
<term>Terminal aryl substituents</term>
<term>Transfer oxygenative cyclization</term>
<term>Univ</term>
<term>Verlag</term>
<term>Verlag gmbh</term>
<term>Weinheim</term>
<term>Weinheim cheminform</term>
<term>Yamamoto</term>
<term>Yamashita</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en"><term>Alkyl</term>
<term>Bicyclic</term>
<term>Bicyclic furan skeletons</term>
<term>Bicyclic furans</term>
<term>Broad spectrum</term>
<term>Chem</term>
<term>Cheminform</term>
<term>Chikusa</term>
<term>Cyclization</term>
<term>Diynes</term>
<term>Dmso</term>
<term>Edented</term>
<term>Furan</term>
<term>Furan derivatives</term>
<term>Furan oxygen</term>
<term>Gmbh</term>
<term>Kgaa</term>
<term>Lindner</term>
<term>Lindner cheminform</term>
<term>Nagoya</term>
<term>Nagoya univ</term>
<term>Nishiyama</term>
<term>Oligoaryl</term>
<term>Optimized</term>
<term>Optimized conditions dmso</term>
<term>Oxygenative</term>
<term>Pharm</term>
<term>Ruthenacycle</term>
<term>Ruthenacyclopentatriene</term>
<term>Substituents</term>
<term>Terminal alkyl substituents</term>
<term>Terminal aryl substituents</term>
<term>Transfer oxygenative cyclization</term>
<term>Univ</term>
<term>Verlag</term>
<term>Verlag gmbh</term>
<term>Weinheim</term>
<term>Weinheim cheminform</term>
<term>Yamamoto</term>
<term>Yamashita</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Generally, a broad spectrum of bicyclic furan skeletons can be obtained from diynes bearing 2 terminal aryl substituents under the optimized conditions A)‐C).</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/EdenteV2/Data/Istex/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 005B27 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Curation/biblio.hfd -nk 005B27 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= EdenteV2 |flux= Istex |étape= Curation |type= RBID |clé= ISTEX:B727252C6C8053759EF768BA72D72C739385037A |texte= ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene. }}
![]() | This area was generated with Dilib version V0.6.32. | ![]() |