| Literature DB >> 30427692 |
Rei Tomifuji1, Kazuki Maeda1, Toshifumi Takahashi1, Takuya Kurahashi1, Seijiro Matsubara1.
Abstract
The aza-Diels-Alder reaction of nonactivated dienes and imines was realized through the action of the ion-paired Lewis acid catalyst [FeCl2]+[FeCl4]- generated by the in situ disproportionation of FeCl3. The uniquely high reactivity of [FeCl2]+[FeCl4]- was attributed to both the highly Lewis acidic FeCl2+ and thermodynamically stable FeCl4- acting as an ion-paired catalyst. Synchrotron-based X-ray absorption fine structure measurements provided fundamental insights into the disproportionation and structure of the resulting ion-paired iron complex. A theoretical study was performed to analyze the catalytic reaction and better understand the "ion-pairing effect" which transforms simple FeCl3 into a high turnover frequency Lewis acid catalyst in the aza-Diels-Alder reaction of nonactivated dienes and imines.Entities:
Year: 2018 PMID: 30427692 DOI: 10.1021/acs.orglett.8b03249
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005