Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands.
Org Biomol Chem. 2010 Sep 7;8(17):3868-73. doi: 10.1039/c005048b. Epub 2010 Jun 25.
A kinetic study of DNA-based catalytic enantioselective Friedel-Crafts alkylation and Michael addition reactions showed that DNA affects the rate of these reactions significantly. Whereas in the presence of DNA, a large acceleration was found for the Friedel-Crafts alkylation and a modest acceleration in the Michael addition of dimethyl malonate, a deceleration was observed when using nitromethane as nucleophile. Also, the enantioselectivities proved to be dependent on the DNA sequence. In comparison with the previously reported Diels-Alder reaction, the results presented here suggest that DNA plays a similar role in both cycloaddition and conjugate addition reactions.
基于 DNA 的催化对映选择性 Frie-del-Crafts 烷基化和迈克尔加成反应的动力学研究表明,DNA 显著影响这些反应的速率。在 DNA 的存在下,Frie-del-Crafts 烷基化反应得到了很大的加速,而在二甲基丙二酸的迈克尔加成中则得到了适度的加速,而当使用硝基甲烷作为亲核试剂时,则观察到了减速。此外,对映选择性也被证明依赖于 DNA 序列。与之前报道的 Diels-Alder 反应相比,这里提出的结果表明 DNA 在环加成和共轭加成反应中都发挥了类似的作用。