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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 : 005B28

ChemInform 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.

RBID : ISTEX:B727252C6C8053759EF768BA72D72C739385037A

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:

https://api.istex.fr/document/B727252C6C8053759EF768BA72D72C739385037A/fulltext/pdf

DOI: 10.1002/chin.201239103

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ISTEX:B727252C6C8053759EF768BA72D72C739385037A

Le document en format XML

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<author><name sortKey="Yamashita, Ken" sort="Yamashita, Ken" uniqKey="Yamashita K" first="Ken" last="Yamashita">Ken Yamashita</name>
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<term>Verlag</term>
<term>Verlag gmbh</term>
<term>Weinheim</term>
<term>Weinheim cheminform</term>
<term>Yamamoto</term>
<term>Yamashita</term>
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<term>Chikusa</term>
<term>Cyclization</term>
<term>Diynes</term>
<term>Dmso</term>
<term>Edented</term>
<term>Furan</term>
<term>Furan derivatives</term>
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<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>
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<term>Pharm</term>
<term>Ruthenacycle</term>
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<term>Univ</term>
<term>Verlag</term>
<term>Verlag gmbh</term>
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ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.

ChemInform Abstract: Ruthenium‐Catalyzed Transfer Oxygenative Cyclization of α,ω‐Diynes: Unprecedented [2 + 2 + 1] Route to Bicyclic Furans via Ruthenacyclopentatriene.

Source :

English descriptors

Abstract

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