Synthesis of various N-heterocycles using the four-component Ugi reaction
| Autor: | M Heravi, Majid, Mohammadkhani, L |
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| Rok vydání: | 2019 |
| Předmět: |
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5-Diketopiperazines Ugi reaction Nitrogen-containing heterocycle Ugi adduct Post-Ugi transformation Cyclization Multicomponent reaction MCRs β-lactams Pyrrolidinones Pyrrolinones Pyrrolidinediones Pyrrolidine Oxazole Indolin-2-ones Isoindoline-2-ones Benzimidazoles 2 5-Diketopiperazines Quinolines Isoquinolines Benzoxazinones Pyrrolopyridines Quinoxalinones Benzazepines Benzoxazepinones Triazolobenzodiazepines Spiroindolines Benzazepines |
| Popis: | Nowadays, among synthetic organic chemists, the Ugi four-component reaction (U-4CR), is known as the most important and useful isocyanide-based multicomponent reactions (IMCRs); since it allows the rapid and straightforward synthesis of the linear peptide backbone. U-4CR, actually is the condensation reaction involving, an isocyanide, an aldehyde, an amine, and a carboxylic acid leading to the formation of the corresponding adduct. Significantly, this adduct can be cyclized through a suitable posttransformation, resulting in the construction of different heterocyclic systems containing nitrogen. In this chapter, we try to underscore the use of post-Ugi transformation in the synthesis of various N-heterocycles with four-, five-, six-, and seven-membered rings as well as fused heterocycles bearing one or two heteroatoms. |
| Databáze: | OpenAIRE |
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