Dasgupta Ayan, Babaahmadi Rasool, Pahar Sanjukta, Stefkova Katarina, Gierlichs Lukas, Yates Brian F, Ariafard Alireza, Melen Rebecca L
Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, United Kingdom.
School of Physical Sciences, University of Tasmania, Private Bag 75, Hobart, Tasmania, 7001, Australia.
Angew Chem Int Ed Engl. 2021 Nov 8;60(46):24395-24399. doi: 10.1002/anie.202109744. Epub 2021 Oct 12.
In recent years, metal-free organic synthesis using triarylboranes as catalysts has become a prevalent research area. Herein we report a comprehensive computational and experimental study for the highly selective synthesis of N-substituted pyrazoles through the generation of carbenium species from the reaction between aryl esters and vinyl diazoacetates in the presence of catalytic tris(pentafluorophenyl)borane [B(C F ) ]. DFT studies were undertaken to illuminate the reaction mechanism revealing that the in situ generation of a carbenium species acts as an autocatalyst to prompt the regiospecific formation of N-substituted pyrazoles in good to excellent yields (up to 81 %).
近年来,使用三芳基硼烷作为催化剂的无金属有机合成已成为一个热门的研究领域。在此,我们报告了一项全面的计算和实验研究,该研究通过在催化量的三(五氟苯基)硼烷[B(C₆F₅)₃]存在下,芳基酯与乙烯基重氮乙酸酯反应生成碳正离子物种,从而实现N-取代吡唑的高选择性合成。进行了密度泛函理论(DFT)研究以阐明反应机理,结果表明碳正离子物种的原位生成充当自催化剂,促使N-取代吡唑以良好至优异的产率(高达81%)区域特异性地形成。