Stereoselective Synthesis of 2‐Oxyenamides **
Abstract: An improved route for the highly stereoselective synthesis of (Z)‐2‐oxyenamides is reported. The desired products can be accessed in only three steps from aminoacetaldehyde dimethyl acetal as common, readily available building block in a highly modular fashion. The improved procedure has been applied to the synthesis of various acylated and sufonylated oxyenamides. Mechanistic and theoretical studies provide a conclusive rationale for the observed stereoselectivities.
- 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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Stereoselective Synthesis of 2‐Oxyenamides ** ; volume:2022 ; number:31 ; year:2022 ; extent:7
European journal of organic chemistry ; 2022, Heft 31 (2022) (gesamt 7)
- Creator
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Krieg, Sara‐Cathrin
Grimmer, Jennifer
Pick, Annika Maria
Kelm, Harald
Breugst, Martin
Manolikakes, Georg
- DOI
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10.1002/ejoc.202200772
- URN
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urn:nbn:de:101:1-2022081715301871964136
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:22 AM CEST
Data provider
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Associated
- Krieg, Sara‐Cathrin
- Grimmer, Jennifer
- Pick, Annika Maria
- Kelm, Harald
- Breugst, Martin
- Manolikakes, Georg
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