Construction of chiral α- tert -amine scaffolds via amine-catalyzed asymmetric Mannich reactions of alkyl-substituted ketimines
Stereoselective Mannich reactions of aldehydes with ketimines provide chiral β-amino aldehydes that bear an α- -amine moiety. However, the structural variation of the ketimines is limited due to the formation of inseparable / isomers, low reactivity, and other synthetic difficulties. In this study,...
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Veröffentlicht in: | Chemical science (Cambridge) 2021-01, Vol.12 (4), p.1445-1450 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Stereoselective Mannich reactions of aldehydes with ketimines provide chiral β-amino aldehydes that bear an α-
-amine moiety. However, the structural variation of the ketimines is limited due to the formation of inseparable
/
isomers, low reactivity, and other synthetic difficulties. In this study, a highly diastereodivergent synthesis of hitherto difficult-to-access β-amino aldehydes that bear a chiral α-
-amine moiety was achieved using the amine-catalyzed Mannich reactions of aldehydes with less-activated
-ketimines that bear both alkyl and alkynyl groups. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d0sc05269h |