Seoane Andrés, Mascareñas José Luis
Centro Singular de Investigación Química Biolóxica e Materiais Moleculares (CIQUS) Departamento de Química Orgánica. Universidade de Santiago de Compostela 15782 Santiago de Compostela A Coruña Spain.
European J Org Chem. 2022 Aug 26;2022(32):e202200118. doi: 10.1002/ejoc.202200118. Epub 2022 May 12.
The possibility of performing designed transition-metal catalyzed reactions in biological and living contexts can open unprecedented opportunities to interrogate and interfere with biology. However, the task is far from obvious, in part because of the presumed incompatibly between organometallic chemistry and complex aqueous environments. Nonetheless, in the past decade there has been a steady progress in this research area, and several transition-metal (TM)-catalyzed bioorthogonal and biocompatible reactions have been developed. These reactions encompass a wide range of mechanistic profiles, which are very different from those used by natural metalloenzymes. Herein we present a summary of the latest progress in the field of TM-catalyzed bioorthogonal reactions, with a special focus on those triggered by activation of multiple carbon-carbon bonds.
在生物和生命环境中进行设计好的过渡金属催化反应的可能性,能够为探究和干预生物学开启前所未有的机遇。然而,这项任务绝非易事,部分原因在于有机金属化学与复杂的水性环境之间可能存在不相容性。尽管如此,在过去十年里,该研究领域取得了稳步进展,并且已经开发出了几种过渡金属(TM)催化的生物正交和生物相容反应。这些反应涵盖了广泛的机理类型,与天然金属酶所使用的机理截然不同。在此,我们总结了过渡金属催化的生物正交反应领域的最新进展,特别关注那些由多个碳 - 碳键活化引发的反应。