Atroposelective Synthesis of 2,2′-Bis(arylamino)-1,1′-biaryls by Oxidative Iron(III)- and Phosphoric Acid-Catalyzed C−C Coupling of Diarylamines**
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
Abstract
We describe an iron-catalyzed asymmetric oxidative C−C coupling of diarylamines which proceeds at room temperature with air as final oxidant. Using hexadecafluorophthalocyanine-iron(II) as catalyst in the presence of catalytic amounts of an axially chiral biarylphosphoric acid, the resulting chiral 2,2′-diamino-1,1′-biaryls are obtained in up to 90 % ee as confirmed by chiral HPLC. A detailed mechanism has been proposed with a radical cation-chiral phosphate ion pair as key intermediate leading to the observed asymmetric induction.
Details
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | e202203269 |
| Fachzeitschrift | Chemistry - A European Journal |
| Jahrgang | 29 |
| Ausgabenummer | 6 |
| Publikationsstatus | Veröffentlicht - 27 Jan. 2023 |
| Peer-Review-Status | Ja |
Externe IDs
| PubMed | 36269611 |
|---|
Schlagworte
ASJC Scopus Sachgebiete
Schlagwörter
- asymmetric catalysis, biaryl compounds, C−H bond activation, iron, phthalocyanines