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Elsevier, Tetrahedron Letters, 23(53), p. 2876-2880

DOI: 10.1016/j.tetlet.2012.03.122

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Novel diversely substituted 1-heteroaryl-2-imidazolines for fragment-based drug discovery

Journal article published in 2012 by Mikhail Krasavin ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A palladium-catalyzed Buchwald–Hartwig arylation protocol has been applied to achieve high-yielding N-heteroarylation of a diverse set of privileged 2-imidazolines. The resulting compounds are of interest as a novel type of molecular tool for fragment-based drug discovery. The potential for combining two 2-imidazoline moieties in a heteroarene-linked dimer via sequential Pd-catalyzed arylation has been demonstrated