Organocatalyzed Asymmetric Conjugate Addition of Cyclic β‐Keto Esters to (E)‐β‐Nitroacrylate Derivatives
Abstract: A diaminomethylenemalononitrile organocatalyst efficiently promoted the asymmetric conjugate addition of cyclic β‐keto esters to (E)‐β‐nitroacrylate derivatives, yielding the corresponding β‐nitro esters derivatives with excellent enantioselectivities (up to >99 % ee). This is the first successful example of highly stereoselective conjugate addition of cyclic β‐keto esters to (E)‐β‐nitroacrylate derivatives to obtain anti‐isomers.
- 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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Organocatalyzed Asymmetric Conjugate Addition of Cyclic β‐Keto Esters to (E)‐β‐Nitroacrylate Derivatives ; day:12 ; month:11 ; year:2024 ; extent:6
Chemistry ; (12.11.2024) (gesamt 6)
- Creator
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Matsushima, Yasuyuki
Iijima, Yoshiyuki
Tanabe, Chinatsu
Nakashima, Kosuke
Hirashima, Shin‐ichi
Miura, Tsuyoshi
- DOI
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10.1002/asia.202401029
- URN
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urn:nbn:de:101:1-2411131322155.787960069043
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:21 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Matsushima, Yasuyuki
- Iijima, Yoshiyuki
- Tanabe, Chinatsu
- Nakashima, Kosuke
- Hirashima, Shin‐ichi
- Miura, Tsuyoshi