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New Entry to the Synthesis of α‑Iminonitriles by Lewis Acid Mediated Isomerization of Cyano-Substituted Iminoisobenzofurans Prepared by Palladium-Catalyzed Three-Component Coupling of Arynes, Isocyanides, and Cyanoformates

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Figshare2016-02-17 更新2026-04-29 收录
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https://figshare.com/articles/dataset/New_Entry_to_the_Synthesis_of_Iminonitriles_by_Lewis_Acid_Mediated_Isomerization_of_Cyano_Substituted_Iminoisobenzofurans_Prepared_by_Palladium_Catalyzed_Three_Component_Coupling_of_Arynes_Isocyanides_and_Cyanoformates/2274865
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A variety of α-iminonitriles were formed as the minor products of three-component coupling reactions of arynes, isocyanides, and cyanoformates in the presence of the cationic palladium complex [Pd­(NCPh)2(dppf)]­(BF4)2 as the catalyst, along with cyano-substituted iminoisobenzofurans as the major products. α-Iminonitriles obtained from this process are hardly accessible by conventional methods. In addition, when the isolated iminoisobenzofurans were treated with diisobutylaluminum hydride (DIBAL-H) or AlMe3, the transformation of cyano-substituted iminoisobenzofurans into α-iminonitriles was observed.
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2016-02-17
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