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Iron‐Catalyzed Oxidative C−O and C−N Coupling Reactions Using Air as Sole Oxidant **
Author(s) -
Purtsas Alexander,
Rosenkranz Marco,
Dmitrieva Evgenia,
Kataeva Olga,
Knölker HansJoachim
Publication year - 2022
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202104292
Subject(s) - amination , regioselectivity , oxidative phosphorylation , chemistry , catalysis , oxidative coupling of methane , phenols , medicinal chemistry , organic chemistry , combinatorial chemistry , biochemistry
We describe the oxygenation of tertiary arylamines, and the amination of tertiary arylamines and phenols. The key step of these coupling reactions is an iron‐catalyzed oxidative C−O or C−N bond formation which generally provides the corresponding products in high yields and with excellent regioselectivity. The transformations are accomplished using hexadecafluorophthalocyanine−iron(II) (FePcF 16 ) as catalyst in the presence of an acid or a base additive and require only ambient air as sole oxidant.
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