4.4 Article

Construction of Tetrazole Derivatives via Sequential Ugi-N3/Pd-Catalyzed Isocyanide Insertion Reactions

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CHEMISTRYSELECT
卷 8, 期 5, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202204294

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Tetrazole derivatives; Pd-catalyst; MCR reactions; isocyanide insertion; antifungal activities

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A straightforward method for the construction of tetrazole derivatives was achieved through Pd-catalyzed isocyanide insertion reactions, providing an extension for the response of multi-molecule isocyanides. The Ugi-N-3 reaction was introduced to enrich the diversity of skeleton structures. The commercially available starting materials and moderate to good yields make this method a valuable tool for generating N-containing heterocyclic compounds.
Herein, a straightforward method for the construction of tetrazole derivatives has been achieved through Pd-catalyzed isocyanide insertion reactions, which is a good extension for the response of multi-molecule isocyanides. The Ugi-N-3 reaction was introduced to the transformation to enrich the diversity of skeleton structures. The commercially available starting materials and moderate to good yields make this method a valuable tool for generating N-containing heterocyclic compounds.

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