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    <subfield code="a">Guzmán, Jefferson</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-9340-5952</subfield>
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    <subfield code="a">Selective reduction of formamides to O-silylated hemiaminals or methylamines with HSiMe2Ph catalyzed by iridium complexes</subfield>
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    <subfield code="c">2019</subfield>
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    <subfield code="a">The reaction of (4-methyl-pyridin-2-iloxy)ditertbutylsilane (NSi tBu -H, 1) with [IrCl(coe) 2 ] 2 affords the iridium(iii) complex [Ir(H)(Cl)(¿ 2 -NSi tBu )(coe)] (2), which has been fully characterized including X-ray diffraction studies. The reaction of 2 with AgCF 3 SO 3 leads to the formation of species [Ir(H)(CF 3 SO 3 )(¿ 2 -NSi tBu )(coe)] (3). The iridium complexes 2 and 3 are effective catalysts for the reduction of formamides with HSiMe 2 Ph. The selectivity of the reduction process depends on the catalyst. Thus, by using complex 2, with a chloride ancillary ligand, it has been possible to selectively obtain the corresponding O-silylated hemiaminal by reaction of formamides with one equivalent of HSiMe 2 Ph, while complex 3, with a triflate ligand instead of chloride, catalyzed the selective reduction of formamides to the corresponding methylamine.</subfield>
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    <subfield code="a">Inorganic Chemistry</subfield>
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    <subfield code="a">Bernal, Ana M.</subfield>
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    <subfield code="a">García-Orduña, Pilar</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Lahoz, Fernando J.</subfield>
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    <subfield code="a">Oro, Luis A.</subfield>
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    <subfield code="a">Fernández-Alvarez, Francisco J.</subfield>
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    <subfield code="1">2010</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Inorgánica</subfield>
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    <subfield code="1">2012</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
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    <subfield code="g">48, 13 (2019), 4255-4262</subfield>
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