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EnglishOver the last thirty years organic azides have drawn a great deal of attention as radical traps for carbon- and heteroatom-centered radicals, both in intra and in intermolecular processes. The resulting intermediates (nitrogen-centered radicals such as triazenyls, aminyls, or even iminyls) can be conveniently employed in the synthesis of a variety of cyclic and acyclic nitrogen- containing compounds.
| Titolo: | From Azides to Nitrogen-Centered Radicals: Applications of Azide Radical Chemistry to Organic Synthesis |
| Autore/i: | MINOZZI, MATTEO; NANNI, DANIELE; SPAGNOLO, PIERO |
| Autore/i Unibo: | |
| Anno: | 2009 |
| Rivista: | |
| Digital Object Identifier (DOI): | http://dx.doi.org/10.1002/chem.200802710 |
| Abstract: | Over the last thirty years organic azides have drawn a great deal of attention as radical traps for carbon- and heteroatom-centered radicals, both in intra and in intermolecular processes. The resulting intermediates (nitrogen-centered radicals such as triazenyls, aminyls, or even iminyls) can be conveniently employed in the synthesis of a variety of cyclic and acyclic nitrogen- containing compounds. |
| Data prodotto definitivo in UGOV: | 2009-10-12 18:28:10 |
| Appare nelle tipologie: | 1.01 Articolo in rivista |
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http://hdl.handle.net/11585/77795
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