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5-Nitroisoxazoles in S<sub>N</sub>Ar reactions: access to polysubstituted isoxazole derivatives

Dmitry A. Vasilenko, Sevastian E. Dronov, Dzianis U. Parfiryeu, Kirill S. Sadovnikov, Kseniya N. Sedenkova, Yuri K. Grishin, Victor B. Rybakov, Tamara S. Kuznetsova, Elena B. Averina

2021Organic & Biomolecular Chemistry12 citationsDOI

Abstract

An efficient protocol for the straightforward functionalization of the isoxazole ring via the reactions of aromatic nucleophilic substitution of the nitro group with various nucleophiles has been elaborated. The method features excellent chemical yields, easy operability of the reaction, mild reaction conditions and a broad scope of both 5-nitroisoxazoles and nucleophiles. A synthetic approach to 3,5- and 3,4,5-substituted isoxazoles via the sequential functionalization of the isoxazole ring has been developed based on the excellent regioselectivity of the reaction of 3,5-dinitroisoxazoles with nucleophiles.

Topics & Concepts

IsoxazoleChemistryComputer scienceMedicinal chemistryCombinatorial chemistryChemical Reaction MechanismsChemical Synthesis and AnalysisCoordination Chemistry and Organometallics
5-Nitroisoxazoles in S<sub>N</sub>Ar reactions: access to polysubstituted isoxazole derivatives | Litcius