Diastereoselective Thia-Claisen Rearrangement of Pyrrolidinone-Derived Ketene N,S-Acetals
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Diastereoselective Thia-Claisen Rearrangement of Pyrrolidinone-Derived Ketene N,S-Acetals ; volume:2009 ; number:18 ; year:2009 ; pages:3052-3052
Synlett ; 2009, Heft 18 (2009), 3052-3052
- DOI
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10.1055/s-0029-1218336
- URN
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urn:nbn:de:101:1-2019020511372622118864
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
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Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?
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A Wittig-olefination–Claisen-rearrangement approach to the 3-methylquinoline-4-carbaldehyde synthesis
Organocatalytic Asymmetric Claisen Rearrangement
Nickel-Catalyzed Asymmetric Claisen Rearrangement
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The Claisen rearrangement : methods and applications
Diazaphospholene-Catalyzed Reductive Ireland–Claisen Rearrangement
Alkene Isomerization Revitalizes the Coates–Claisen Rearrangement
Alkene Isomerization Revitalizes the Coates–Claisen Rearrangement
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Brønsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement
Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?
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