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The 1,3‐dipolar cycloadditions of azomethine‐ylides and ‐imines, nitrones, nitrilimines, and azides catalysed by inorganic nanoparticles are described. Emphasis is given to the nanometric catalysts involved, their structure, characterisation, and recyclability and, when remarkable, their preparation. Whenever possible, the improvements with respect to cycloadditions performed with the usual (non‐nano) catalysts are discussed.
aqueous media, green chemistry, Aqueous media; Dipolar cycloadditions; Green chemistry; Nanocatalysis; Nanoparticles, nanoparticles, Dipolar cycloadditions, nanocatalysis
aqueous media, green chemistry, Aqueous media; Dipolar cycloadditions; Green chemistry; Nanocatalysis; Nanoparticles, nanoparticles, Dipolar cycloadditions, nanocatalysis
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 9 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% | 
