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Rearrangement of Pyridine to Its 2-Carbene Tautomer Mediated by Iridium

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Rearrangement_of_Pyridine_to_Its_2_Carbene_Tautomer_Mediated_by_Iridium/2973625
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One of the Ir−CH2 bonds within the chelate structure of compound 1 acts as a C−H activation shuttle and permits the 1,2-H shift needed for the isomerization of pyridine to its 2-carbene tautomer. The iridium-mediated tautomerization is kinetically competitive with traditionally facile N coordination of the heterocycle.
创建时间:
2016-02-28
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