cheminform abstract: efficient hydrosilylation of carbonyl compounds with the simple amide catalyst...

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ChemInform 2011, 42, issue 18 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Hydrosilylation O 0278 DOI: 10.1002/chin.201118042 Efficient Hydrosilylation of Carbonyl Compounds with the Simple Amide Cata- lyst [Fe{N(SiMe3)2}2]. — Fe(NTms2)2 represents a novel cost-effective, environmen- tally benign catalyst for the hydrosilylation of carbonyl compounds at room tempera- ture. No neutral donor ligand or activator is required. A wide range of functional groups is tolerated, including ether, olefin, cyclopropyl, aromatic bromine, dimethylamino or nitrile groups. — (YANG, J.; TILLEY*, T. D.; Angew. Chem., Int. Ed. 49 (2010) 52, 10186-10188, http://dx.doi.org/10.1002/anie.201005055 ; Dep. Chem., Univ. Calif., Berkeley, CA 94720, USA; Eng.) — Mischke 18- 042

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HydrosilylationO 0278 DOI: 10.1002/chin.201118042

Efficient Hydrosilylation of Carbonyl Compounds with the Simple Amide Cata-lyst [Fe{N(SiMe3)2}2]. — Fe(NTms2)2 represents a novel cost-effective, environmen-tally benign catalyst for the hydrosilylation of carbonyl compounds at room tempera-ture. No neutral donor ligand or activator is required. A wide range of functional groups is tolerated, including ether, olefin, cyclopropyl, aromatic bromine, dimethylamino or nitrile groups. — (YANG, J.; TILLEY*, T. D.; Angew. Chem., Int. Ed. 49 (2010) 52, 10186-10188, http://dx.doi.org/10.1002/anie.201005055 ; Dep. Chem., Univ. Calif., Berkeley, CA 94720, USA; Eng.) — Mischke

18- 042

ChemInform 2011, 42, issue 18 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim