Keto-Enol Tautomerism in Passerini and Ugi Adducts

Keto-Enol Tautomerism in Passerini and Ugi Adducts

The use of arylglyoxal as starting material in Passerini and Ugi reactions affords β-ketoamides. This has allowed to study keto-enol tautomerism in these systems and assess the way in which the presence of acyloxy or aminoacyl groups bound to the C2 position affects such tautomerism, and to investig...

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Bibliographic Details
Main Authors: Pablo Pertejo, Andrea Sancho-Medina, Tomás Hermosilla, Beatriz González-Saiz, Javier Gómez-Ayuso, Roberto Quesada, Daniel Moreno, Israel Carreira-Barral, María García-Valverde
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Molecules
Subjects:
Keto-enol tautomerism
Passerini adduct
Ugi adduct
lactone
lactame
2-hydroxyglutaric acid
Online Access:https://www.mdpi.com/1420-3049/26/4/919

Internet

https://www.mdpi.com/1420-3049/26/4/919

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