Selective hydrosilylation of ketones catalyzed by in situ-generated iron NHC complexes (Articolo in rivista)

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  • Selective hydrosilylation of ketones catalyzed by in situ-generated iron NHC complexes (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/aoc.1832 (literal)
Alternative label
  • Buitrago, Elina; Adolfsson, Hans; Zani, Lorenzo (2011)
    Selective hydrosilylation of ketones catalyzed by in situ-generated iron NHC complexes
    in Applied organometallic chemistry (Online); John Wiley & Sons Ltd., Chichester (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Buitrago, Elina; Adolfsson, Hans; Zani, Lorenzo (literal)
Pagina inizio
  • 748 (literal)
Pagina fine
  • 752 (literal)
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  • http://onlinelibrary.wiley.com/doi/10.1002/aoc.1832/abstract (literal)
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  • 25 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 5 (literal)
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  • 10 (literal)
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  • Department of Organic Chemistry, Stockholm University, the Arrhenius Laboratory, SE-10691 Stockholm, Sweden; Institute for the Chemistry of Organometallic Compounds (CNR-ICCOM), Via Madonna del Piano 10, I-50019, Sesto Fiorentino, Florence, Italy (literal)
Titolo
  • Selective hydrosilylation of ketones catalyzed by in situ-generated iron NHC complexes (literal)
Abstract
  • Aryl alkyl-, heteroaryl alkyl- and dialkyl ketones were readily reduced to their corresponding secondary alcohols in high yields, using the commercially available and inexpensive polymeric silane polymethylhydrosiloxane (PMHS), as reducing agent. The reaction is catalyzed by an in situ-generated iron complex, conveniently generated from iron(II) acetate and the commercially available N-heterocyclic carbene (NHC) precursor IPr·HCl. (literal)
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