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Conversion of Ni(II)-Allylporphyrins to α,β-Unsaturated Formylporphyrins via a Nickel-Promoted Reaction

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Conversion_of_Ni_II_Allylporphyrins_to_Unsaturated_Formylporphyrins_via_a_Nickel_Promoted_Reaction/2998066
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A new route to α,β-unsaturated formylporphyrins begins with the synthesis of allyl-substituted porphyrins via the Suzuki cross-coupling reaction of bromoporphyrins and allylboronic acid pinacol ester in 50−95% yield. Treatment of allyl-substituted porphyrins with nickel acetate in N,N-dimethylformamide (DMF) then affords mono- and diacroleinylporphyrins in up to 70% yield.
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2007-07-06
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