Mulliken Center for Theoretical Chemistry, University of Bonn, Beringstr. 4+6, 53115, Bonn, Germany.
Chemistry. 2020 Aug 6;26(44):10140-10151. doi: 10.1002/chem.202002656. Epub 2020 Jul 23.
In this work the mechanism of the aldehyde umpolung reactions, catalyzed by azolium cations in the presence of bases, was studied through computational methods. Next to the mechanism established by Breslow in the 1950s that takes effect through the formation of a free carbene, we have suggested that these processes can follow a concerted asynchronous path, in which the azolium cation directly reacts with the substrate, avoiding the formation of the carbene intermediate. We hereby show that substituting the azolium cation, and varying the base or the substrate do not affect the preference for the concerted reaction mechanism. The concerted path was found to exhibit low barriers also for the reactions of thiamine with model substrates, showing that this path might have biological relevance. The dominance of the concerted mechanism can be explained through the specific structure of the key transition state, avoiding the liberation of the highly reactive, and thus unstable carbene lone pair, whereas activating the substrate through hydrogen-bonding interactions. Polar and hydrogen-bonding solvents, as well as the presence of the counterions of the azolium salts facilitate the reaction through carbenes, bringing the barriers of the two reaction mechanisms closer, in many cases making the concerted path less favorable. Thus, our data show that by choosing the exact components in a reaction, the mechanism can be switched to occur with or without carbenes.
在这项工作中,通过计算方法研究了在碱存在下,唑鎓阳离子催化的醛反转反应的机理。除了 Breslow 在 20 世纪 50 年代提出的通过形成游离碳烯起作用的机理外,我们还提出这些过程可以遵循协同异步途径,其中唑鎓阳离子直接与底物反应,避免形成碳烯中间体。我们在此表明,取代唑鎓阳离子并改变碱或底物不会影响对协同反应机理的偏好。对于与模型底物的硫胺素反应,协同途径也表现出较低的障碍,表明该途径可能具有生物学相关性。协同机制的主导地位可以通过关键过渡态的特定结构来解释,从而避免释放高度反应性且因此不稳定的碳烯孤对,同时通过氢键相互作用激活底物。极性和氢键溶剂以及唑鎓盐的抗衡离子的存在通过碳烯促进反应,使两种反应机制的障碍更加接近,在许多情况下使协同途径变得不那么有利。因此,我们的数据表明,通过选择反应中的精确组分,可以切换反应机制以发生或不发生碳烯。