Development of a New Catalyst for the Distannation of Alkynes
Identifieur interne : 000B83 ( Main/Exploration ); précédent : 000B82; suivant : 000B84Development of a New Catalyst for the Distannation of Alkynes
Auteurs : Sascha Braune ; Uli Kazmaier [Allemagne]Source :
- Angewandte Chemie International Edition [ 1433-7851 ] ; 2003-01-20.
English descriptors
- KwdEn :
- Teeft :
- Absolute toluene, Alkyne, Angew, Calcd, Catalyst, Chem, Chemischen industrie, Deutsche forschungsgemeinschaft, Distannation, Distannylated, Distannylated product, Flash chromatography, Hydride, Hydrostannation, Isonitrile, Kazmaier, Mmol, Molybdenum, Phenyl, Phenyl isocyanide, Phenyl ring, Pohlman, Propargylic, Propargylic esters, Schau, Selectivity, Tributyltin, Tributyltin hydride, Tungsten isonitrile, Verlag gmbh, Weinheim.
Abstract
An added bonus in the optimization of a catalyst for the hydrostannation with tin hydrides was the discovery that molybdenum isonitrile complexes are also suitable for distannations. Further developments in this respect led to a new tungsten isonitrile complex, which catalyzed this reaction highly efficiently and selectively (see scheme, THP=tetrahydropyranyl).
Url:
DOI: 10.1002/anie.200390102
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Istex, to step Curation: 001340
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- to stream Main, to step Curation: 000B83
Le document en format XML
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<front><div type="abstract">An added bonus in the optimization of a catalyst for the hydrostannation with tin hydrides was the discovery that molybdenum isonitrile complexes are also suitable for distannations. Further developments in this respect led to a new tungsten isonitrile complex, which catalyzed this reaction highly efficiently and selectively (see scheme, THP=tetrahydropyranyl).</div>
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