| Literature DB >> 27918127 |
Raphael F Fritsche1, Gabriele Theumer1, Olga Kataeva2, Hans-Joachim Knölker1.
Abstract
We describe iron-catalyzed intermolecular oxidative coupling reactions of diarylamines to form substituted 2,2'-bis(arylamino)biaryl compounds, tetraarylhydrazines, and 5,6-dihydrobenzo[c]cinnolines with the same hexadecafluorinated iron-phthalocyanine catalyst. The mild formation of C-C or N-N bonds was controlled by the use of acidic or basic additives. In contrast to most iron-catalyzed dehydrogenative coupling reactions, ambient air could be used as the sole oxidant. Moreover, iron(III) chloride hexahydrate promoted a one-pot coupling and subsequent intramolecular dearomative coupling to give 10H-spiro[acridine-9,1'-cyclohexa-2',5'-dien-4'-ones].Entities:
Keywords: C−H activation; homogeneous catalysis; iron; phthalocyanines; spiro compounds
Year: 2016 PMID: 27918127 DOI: 10.1002/anie.201610168
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336