School of Physical and Mathematical Sciences, Division of Chemistry and Biological Chemistry, Nanyang Technological University , 21 Nanyang Link, Nanyang 637371, Singapore.
Faculty of Physical Chemistry, University of Belgrade , Studentski Trg 12-16, 11000 Belgrade, Republic of Serbia.
J Org Chem. 2017 Dec 15;82(24):13115-13120. doi: 10.1021/acs.joc.7b02169. Epub 2017 Nov 22.
Selective deuteration of drugs and biologically relevant molecules is becoming increasingly important in the pharmaceutical industry. Site-selective isotopic reinforcement of polyunsaturated fatty acids (PUFAs) at their bis-allylic sites has been identified as a unique approach in preventing oxidative damage in these molecules, which had been linked to neuronal and retinal diseases, atherosclerosis, and aging. Typical methods for preparation of site-selectively deuterated PUFAs require rather long, laborious, and expensive syntheses. In this report, we disclose a very efficient catalytic protocol for site-specific deuteration of PUFAs and analogous poly-alkenes under exceptional kinetic control. Deuterium oxide (DO) has been identified not only as a deuterium source but also as a crucial component in the overall reaction mechanism responsible for averting the formation of thermodynamically favored side-products.
药物和生物相关分子的选择性氘化在制药行业变得越来越重要。在双烯丙基位点对多不饱和脂肪酸(PUFAs)进行位点选择性同位素强化已被确定为防止这些分子氧化损伤的独特方法,这些分子与神经元和视网膜疾病、动脉粥样硬化和衰老有关。典型的制备位点选择性氘化 PUFAs 的方法需要相当长、费力和昂贵的合成。在本报告中,我们公开了一种非常有效的催化方案,可在特殊动力学控制下对 PUFAs 和类似的多烯烃进行位点特异性氘化。重水(DO)不仅被鉴定为氘源,而且还是整个反应机制的关键组成部分,该反应机制负责避免形成热力学有利的副产物。