5411-56-3Relevant articles and documents
Catalytic applications of magnetic nanoparticles functionalized using iridium N-heterocyclic carbene complexes
Iglesias, Diego,Sabater, Sara,Azua, Arturo,Mata, Jose A.
, p. 6437 - 6444 (2015)
A synthetic modular methodology allows the preparation of catalytic materials based on magnetic nanoparticles with iridium N-heterocyclic carbene (NHC) complexes. Imidazolium salts containing a ketone/aldehyde as a pendant functional group are the key species prepared. The condensation reaction of the Cp?IrNHC-CHO compound with magnetic nanoparticles containing amine groups on the surface yields the covalent anchoring of the iridium complex to the surface of the magnetite. The catalytic properties have been evaluated in transfer hydrogenation. The iridium complexes and the material are active in the reduction of ketones using isopropanol as the solvent and hydrogen donor. The catalytic results reveal that the catalytic activity of the material and the molecular complex are equivalent. We have not observed any change in activity due to the support. The recyclability properties of the magnetic material have been evaluated. The results show that the catalyst activity is maintained for two runs. This work describes a simple methodology for anchoring molecular complexes on the surface of magnetic nanoparticles.
The intramolecular reaction of acetophenoneN-tosylhydrazone and vinyl: Br?nsted acid-promoted cationic cyclization toward polysubstituted indenes
Wang, Zhixin,Li, Yang,Chen, Fan,Qian, Peng-Cheng,Cheng, Jiang
, p. 1810 - 1813 (2021/02/27)
In the presence of TsNHNH2, a Br?nsted acid-promoted intramolecular cyclization ofo-(1-arylvinyl) acetophenone derivatives was developed, leading to polysubstituted indenes with complexity and diversity in moderate to excellent yields. In sharp contrast with either the radical or carbene involved cyclization of aldehydicN-tosylhydrazone with vinyl, a cationic cyclization pathway was involved, whereN-tosylhydrazone served as an electrophile and alkylation reagent during this transformation.
Iron-Catalyzed Wacker-type Oxidation of Olefins at Room Temperature with 1,3-Diketones or Neocuproine as Ligands**
Kataeva, Olga,Kn?lker, Hans-Joachim,Linke, Philipp,Puls, Florian
supporting information, p. 14083 - 14090 (2021/05/24)
Herein, we describe a convenient and general method for the oxidation of olefins to ketones using either tris(dibenzoylmethanato)iron(III) [Fe(dbm)3] or a combination of iron(II) chloride and neocuproine (2,9-dimethyl-1,10-phenanthroline) as catalysts and phenylsilane (PhSiH3) as additive. All reactions proceed efficiently at room temperature using air as sole oxidant. This transformation has been applied to a variety of substrates, is operationally simple, proceeds under mild reaction conditions, and shows a high functional-group tolerance. The ketones are formed smoothly in up to 97 % yield and with 100 % regioselectivity, while the corresponding alcohols were observed as by-products. Labeling experiments showed that an incorporated hydrogen atom originates from the phenylsilane. The oxygen atom of the ketone as well as of the alcohol derives from the ambient atmosphere.
