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Hydroboration of Alkynes Catalyzed by Pyrrolide-Based PNP Pincer–Iron Complexes
To utilize iron complexes as catalysts, the application of a well-designed ligand is critical to control the reactivity of the iron center. Recently, our group has succeeded in the synthesis of iron complexes bearing a pyrrolide-based PNP pincer ligand and their application to the catalytic transfor...
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Published in: | Organic letters 2017-08, Vol.19 (16), p.4323-4326 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | To utilize iron complexes as catalysts, the application of a well-designed ligand is critical to control the reactivity of the iron center. Recently, our group has succeeded in the synthesis of iron complexes bearing a pyrrolide-based PNP pincer ligand and their application to the catalytic transformation of dinitrogen into ammonia under mild reaction conditions. As an extensive study, we report the iron-catalyzed hydroboration of alkynes with pinacolborane, where the corresponding E-isomers are obtained selectively. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/acs.orglett.7b01995 |