The synthesis of substituted 1H-tetrazoles from aliphatic or aromatic isonitriles and trimethylsilyl azide can be efficiently promoted by the hexameric capsule of resorcin[ 4]arene as a supramolecular self-assembled catalyst. The reaction is sensitive to the size and nature of the substrate and is driven by encapsulation of the reagents within the cavity of the supramolecular catalyst.

The synthesis of substituted 1H-tetrazoles from aliphatic or aromatic isonitriles and trimethylsilyl azide can be efficiently promoted by the hexameric capsule of resorcin[4]arene as a supramolecular self-assembled catalyst. The reaction is sensitive to the size and nature of the substrate and is driven by encapsulation of the reagents within the cavity of the supramolecular catalyst.

Supramolecular Catalysis in the Synthesis of Substituted 1H-Tetrazoles from Isonitriles by a Self-Assembled Hexameric Capsule

LA SORELLA, GIORGIO;SPERNI, Laura;FABRIS, Fabrizio;STRUKUL, Giorgio;SCARSO, Alessandro
2015-01-01

Abstract

The synthesis of substituted 1H-tetrazoles from aliphatic or aromatic isonitriles and trimethylsilyl azide can be efficiently promoted by the hexameric capsule of resorcin[4]arene as a supramolecular self-assembled catalyst. The reaction is sensitive to the size and nature of the substrate and is driven by encapsulation of the reagents within the cavity of the supramolecular catalyst.
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Descrizione: This is the peer reviewed version of the following article: Supramolecular Catalysis in the Synthesis of Substituted 1H-Tetrazoles from Isonitriles by a Self-Assembled Hexameric Capsule], which has been published in final form at https://onlinelibrary.wiley.com/doi/full/10.1002/ajoc.201402229 This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3627897
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