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À propos de : Regioselective Zirconophosphination of 1-Alkenes: A Versatile Route for the Synthesis of β-Functionalized Alkyldiphenylphosphine Oxides in the Presence of CuCl        

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  • Regioselective Zirconophosphination of 1-Alkenes: A Versatile Route for the Synthesis of β-Functionalized Alkyldiphenylphosphine Oxides in the Presence of CuCl
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  • Zirconocene−alkene complexes Cp2ZrPMe3(CH2CHR) reacted with chlorodiphenyllphosphine to form zircono-ethylphosphine derivatives with high regioselectivity, which could be easily transformed into various functionalized alkyldiarylphosphine oxides in the presence of CuCl.
  • Zirconocene−alkene complexes Cp2Zr(PMe3)(CH2CHR) reacted with chlorodiphenylphosphine to form zircono-ethylphosphine derivatives with high regioselectivity, which could be converted into various β-functionalized alkyldiphenylphosphine oxides in the presence of CuCl.
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  • Regioselective Zirconophosphination of 1-Alkenes
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