Division of Chemistry, Faculty of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8571, Japan.
Angew Chem Int Ed Engl. 2013 Jul 22;52(30):7825-8. doi: 10.1002/anie.201302740. Epub 2013 Jun 14.
Rather crafty: 1,1-Difluoroallenes bearing an aryl group and a cyclopentene moiety undergo indium(III)-catalyzed Friedel-Crafts-type cyclization with subsequent ring expansion and dehydrogenation to afford fluorinated polycyclic aromatic hydrocarbons in high yields. The introduction of an Ar group was effected by in situ halogenation of the intermediary indium species and a subsequent Suzuki-Miyaura reaction.
带有芳基和环戊烯部分的 1,1-二氟烯在铟(III)催化下发生 Friedel-Crafts 型环化反应,随后进行环扩张和脱氢反应,以高产率得到氟化多环芳烃。Ar 基团的引入是通过中间体铟物种的原位卤化和随后的 Suzuki-Miyaura 反应实现的。