2018
DOI: 10.1134/s1070328418040024
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Reactions of Amidoximes with Metal-Activated Nitriles

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Cited by 3 publications
(2 citation statements)
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“…[12,13,14] In this method, the metal ion's reactivity is used to activate and alter a pro-ligand in situ, resulting in coordination compounds with ligands that are generally not accessible via standard organic synthesis. [15,16,17,18,19,20] In this regard, coordination chemists have used nitrile-based ligands to prepare metal complexes, in which they observed the in situ conversion of nitriles into imines, amides, carboxylic acids, and heterocyclic ligands. [21,22,23,24,25] When nitriles are coordinated with metal cations, they become highly susceptible to nucleophilic attack.…”
Section: Introductionmentioning
confidence: 99%
“…[12,13,14] In this method, the metal ion's reactivity is used to activate and alter a pro-ligand in situ, resulting in coordination compounds with ligands that are generally not accessible via standard organic synthesis. [15,16,17,18,19,20] In this regard, coordination chemists have used nitrile-based ligands to prepare metal complexes, in which they observed the in situ conversion of nitriles into imines, amides, carboxylic acids, and heterocyclic ligands. [21,22,23,24,25] When nitriles are coordinated with metal cations, they become highly susceptible to nucleophilic attack.…”
Section: Introductionmentioning
confidence: 99%
“…Numerous research papers have been published in this field. Specifically we would like to highlight the reactivity of coordinated nitriles in the Pt coordination sphere [33][34][35][36][37] or reactivity of triosmium clusters toward a wide range of substrates [38][39][40][41]. UVirradiation (or photolysis) is a well-known technique for a lot of chemical processes, including (i) ligand exchange reactions (e.g., low-valence iron, osmium clusters) [42,43], (ii) ligand transformation [44][45][46], and (iii) CO2 capture [47].…”
Section: Introductionmentioning
confidence: 99%