Formation of Complex α-Imino Esters via Multihetero-Cope Rearrangement­ of α-Keto Ester Derived Nitrones

Abstract A sequential benzoylation and multihetero-Cope rearrangement of α-keto ester derived nitrones has been developed. The reaction furnishes a diverse array of complex α-imino ester derivatives. The products can be transformed into amino alcohols via LiAlH 4 reduction.

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Veröffentlicht in:Synthesis (Stuttgart) 2019-01, Vol.51 (1), p.203-212
Hauptverfasser: Bartlett, Samuel L., Keiter, Kimberly M., Zavesky, Blane P., Johnson, Jeffrey S.
Format: Artikel
Sprache:eng
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Zusammenfassung:Abstract A sequential benzoylation and multihetero-Cope rearrangement of α-keto ester derived nitrones has been developed. The reaction furnishes a diverse array of complex α-imino ester derivatives. The products can be transformed into amino alcohols via LiAlH 4 reduction.
ISSN:0039-7881
1437-210X
DOI:10.1055/s-0037-1610391