Directing Hydrogen Isotope Exchange with Aryl Carboxylic Acids

Synlett Pub Date : 2024-01-05 DOI:10.1055/a-2239-6965
R. Mudd, M. Reid, Laura C. Paterson, J. Atzrodt, V. Derdau, William J. Kerr
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Abstract

A highly effective and selective ortho-directed hydrogen isotope exchange process for aryl carboxylic acids has been achieved using an iridium(I) N-heterocyclic carbene/phosphine complex under mild and neutral conditions. Good levels of deuterium incorporation have been delivered across a wide array of examples, including within a number of biologically active drug compounds.
引导芳基羧酸的氢同位素交换
在温和的中性条件下,利用铱(I)N-杂环碳/膦络合物实现了芳基羧酸的高效和选择性正交定向氢同位素交换过程。在一系列广泛的实例中,包括在一些具有生物活性的药物化合物中,都实现了良好的氘掺入水平。
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