Efficient C2 functionalisation of 2H-2-imidazolines

Robin S. Bon, Nanda E. Sprenkels, Manoe M. Koningstein, Rob F. Schmitz, Frans J. J. de Kanter, Alexander Dömlingꝉ, Marinus B. Groen, Romano V. A. Orrù

Organic & Biomolecular Chemistry · 2007 · 35 citations · 20 references

Concepts

Abstract

Alkylation and oxidation of 2H-2-imidazolines, followed by regioselective deprotection, thionation and microwave-assisted Liebeskind-Srogl reaction, efficiently led to 2-aryl-2-imidazolines as new analogues of p53-hdm2 interaction inhibitors (Nutlins).

References

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