Ugi bisamides based on pyrrolyl-β-chlorovinyl aldehyde: synthesis and reactivity

Authors

  • T. O. Savluk Division of Functional Materials Chemistry, State Scientific Institution "Institute for Single Crystals" of NAS of Ukraine, National Technical University "Kharkiv Polytechnic Institute", Kharkiv, Ukraine
  • V. O. Vereshchak Division of Functional Materials Chemistry, State Scientific Institution "Institute for Single Crystals" of NAS of Ukraine, National Technical University "Kharkiv Polytechnic Institute", Kharkiv, Ukraine
  • V. V. Ananieva Division of Functional Materials Chemistry, State Scientific Institution "Institute for Single Crystals" of NAS of Ukraine, Kharkiv, Ukraine
  • A. V. Tsygankov Division of Functional Materials Chemistry, State Scientific Institution "Institute for Single Crystals" of NAS of Ukraine, National Technical University "Kharkiv Polytechnic Institute", Kharkiv, Ukraine
  • V. A. Chebanov Division of Functional Materials Chemistry, State Scientific Institution "Institute for Single Crystals" of NAS of Ukraine, Faculty of Chemistry, V. N. Karazin Kharkiv National University, Kharkiv, Ukraine

Abstract

The multicomponent Ugi reaction is a powerful tool for creating libraries of organic substances, which may include new biologically active compounds and new components of functional materials [1]. A special role is played by so-called post-Ugi reactions, which allow modification of functional groups and amide bonds in Ugi products [1–3].

References

Erik Van der Eycken Multicomponent Reactions towards Heterocycles: Concepts and Applications / Upendra K. Sharma. – Weinheim.: Wiley-VCH, 2021. – 624 p.

Huang, J. Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One-Pot Approach to Arene-Fused Isoindolinones. EurJOC. 2017, 30, pp 4379–4388.

Chandgude, A. L. 2-Nitrobenzyl Isocyanide as a Universal Convertible Isocyanide. Asian J. Org. Chem. 2017, 6 (7), pp 798–801.

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Published

2024-04-08

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Section

Organic Chemistry