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Microwave-Assisted Synthesis of 1-(5-Substituted-4-hydroxy-2-methyl-1H-pyrrol-3-yl)ethan-1-ones from 2-Amino Acid-Derived Enamine-Type Schiff Bases
1. Introduction Pyrrole-type compounds constitute a broad family of biologically active molecules [1]. Many reports have demonstrated this family’s importance for medicinal chemistry [1,2,3,4] due to their exceptional pharmacological properties. These compounds with a nitrogenous heterocyclic structure have been prominent in drug discovery, especially in therapeutic areas such as oncology, microbiology, and virology.
Attraction Behavior and Functional Response of Orius insidiosus to Semiochemicals Mediating Rose-Western Flower Thrips Interactions
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Untargeted Volatile Profiling Identifies Key Compounds Driving the Attraction of Western Flower Thrips to Alstroemeria Cultivars
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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