Manna Srimanta, Antonchick Andrey P
Abteilung Chemische Biologie, Max-Planck-Institut für Molekulare Physiologie, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany.
Fakultät Chemie und Chemische Biologie, Technische Universität Dortmund, Otto-Hahn-Strasse 4a, 44227, Dortmund, Germany.
Chemistry. 2017 Jun 7;23(32):7825-7829. doi: 10.1002/chem.201701535. Epub 2017 May 19.
Functionalization of C(sp )-H bonds under metal-free reaction conditions is a great challenge due to poor bond reactivity. A novel metal-free oxidative dehydrogenative Diels-Alder reaction of alkylbenzene derivatives with alkenes through C(sp )-H bond functionalization is described. The developed oxidative method provides a straightforward approach to biologically relevant 1,4-phenanthraquinone and isoindole derivatives from readily available starting materials. Furthermore, the synthesis of nitrostyrenes from enylbenzene derivatives by selective C(sp )-H bond functionalization has been demonstrated.
在无金属反应条件下实现C(sp³)-H键的官能团化是一项巨大挑战,因为该键的反应活性较差。本文描述了一种通过C(sp³)-H键官能团化实现烷基苯衍生物与烯烃的新型无金属氧化脱氢狄尔斯-阿尔德反应。所开发的氧化方法提供了一种直接的途径,可从易得的起始原料制备与生物相关的1,4-菲醌和异吲哚衍生物。此外,还证明了通过选择性C(sp³)-H键官能团化从烯基苯衍生物合成硝基苯乙烯。