Literature DB >> 30427692

FeCl3 as an Ion-Pairing Lewis Acid Catalyst. Formation of Highly Lewis Acidic FeCl2+ and Thermodynamically Stable FeCl4- To Catalyze the Aza-Diels-Alder Reaction with High Turnover Frequency.

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


  2 in total

1.  Highly efficient synthesis of 3,4-diarylbutadiene sulfones using Heck-Matsuda reaction.

Authors:  Olga V Shurupova; Sergey A Rzhevskiy; Lidiya I Minaeva; Maxim A Topchiy; Andrey F Asachenko
Journal:  RSC Adv       Date:  2022-02-15       Impact factor: 3.361

2.  The mechanochemical Scholl reaction as a versatile synthesis tool for the solvent-free generation of microporous polymers.

Authors:  Annika Krusenbaum; Sven Grätz; Sarah Bimmermann; Stefanie Hutsch; Lars Borchardt
Journal:  RSC Adv       Date:  2020-07-06       Impact factor: 4.036

  2 in total

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