The Nitrile Imine 1,3-Dipole 2020
DOI: 10.1007/978-3-030-43481-6_4
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Applications of Nitrile Imine Derivatives

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“…Although the majority of the literature focuses on their role in 1,3-dipolar cycloadditions, it has been demonstrated that they can also react with a variety of nucleophiles, including alcohols, amines, and carboxylic acids, to give dimerization reactions, intramolecular rearrangements, and other transformations. [9] Since NIs are unstable, they are typically generated in situ using an appropriate precursor. The most common precursors are hydrazonyl halides [10] and 2,5tetrazoles [11] (Scheme 1), but more modern approaches have also been discovered.…”
Section: Nitrile Imines As 13-dipolesmentioning
confidence: 99%
“…Although the majority of the literature focuses on their role in 1,3-dipolar cycloadditions, it has been demonstrated that they can also react with a variety of nucleophiles, including alcohols, amines, and carboxylic acids, to give dimerization reactions, intramolecular rearrangements, and other transformations. [9] Since NIs are unstable, they are typically generated in situ using an appropriate precursor. The most common precursors are hydrazonyl halides [10] and 2,5tetrazoles [11] (Scheme 1), but more modern approaches have also been discovered.…”
Section: Nitrile Imines As 13-dipolesmentioning
confidence: 99%