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Intermolecular zirconium-catalyzed hydrophosphination of alkenes and dienes with primary phosphines
Michael B Ghebreab1, Christine A Bange, Rory Waterman
1Department of Chemistry, University of Vermont , Burlington, Vermont 05405, United States.
Abstract:
Catalytic hydrophosphination of terminal alkenes and dienes with primary phosphines (RPH2; R = Cy, Ph) under mild conditions has been demonstrated using a zirconium complex, [κ(5)-N,N,N,N,C-(Me3SiNCH2CH2)2NCH2CH2NSiMe2CH]Zr (1). Exclusively anti-Markovnikov functionalized products were observed, and the catalysis is selective for either the secondary or tertiary phosphine (i.e., double hydrophosphination) products, depending on reaction conditions. The utility of the secondary phosphine products as substrates for further elaboration was demonstrated with a platinum-catalyzed asymmetric alkylation reaction.
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