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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1002/adsc.202000514</dc:identifier><dc:language>eng</dc:language><dc:creator>Nolla-Saltiel, R.</dc:creator><dc:creator>Geer, A.M.</dc:creator><dc:creator>Taylor, L.J.</dc:creator><dc:creator>Churchill, O.</dc:creator><dc:creator>Davies, E.S.</dc:creator><dc:creator>Lewis, W.</dc:creator><dc:creator>Blake, A.J.</dc:creator><dc:creator>Kays, D.L.</dc:creator><dc:title>Hydrophosphination of Activated Alkenes by a Cobalt(I) Pincer Complex</dc:title><dc:identifier>ART-2020-118726</dc:identifier><dc:description>Herein we report the synthesis of three heteroleptic first-row transition metal(II) complexes containing carbazolido NNN pincer ligands and conversion to the corresponding metal(I)-carbonyl complexes via a reductive carbonylation route. These complexes are precatalysts for the hydrophosphination of activated alkenes, affording a cobalt-catalysed hydrophosphination process that solely and selectively yields the ß addition (anti-Markovnikov) product. The scope of this transformation has been investigated using a variety of activated alkenes. Isolation and characterisation of substrate-coordinated intermediates reveal available coordination sites, which provide insight into the proposed catalytic cycle.</dc:description><dc:date>2020</dc:date><dc:source>http://zaguan.unizar.es/record/95072</dc:source><dc:doi>10.1002/adsc.202000514</dc:doi><dc:identifier>http://zaguan.unizar.es/record/95072</dc:identifier><dc:identifier>oai:zaguan.unizar.es:95072</dc:identifier><dc:identifier.citation>Advanced Synthesis and Catalysis 362, 15 (2020), 3148-3157</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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