The nitrovinyl moiety is surely one of the most reactive fragments in organic chemistry, continuously employed to explore original pathways and reach new targets. The short review herein represents an update on the potentialities in synthesis of conjugated mononitro or dinitro-1,3-butadienes: in such building blocks, the electrophilicity of the nitrovinyl moiety couples and takes advantage from the presence of a second, conjugated, vinyl moiety, most often leading to the eventual formation of diverse and/or diversely-functionalized heterocycles. The review will thus first of all provide chemists with recent, original protocols to such an important class of organic compounds as heterocycles, materials of choice for a lot of practical applications in different fields of human life.
Recent advances in the use of conjugated nitro or dinitro-1,3-butadienes as building-blocks for the synthesis of heterocycles
Petrillo, Giovanni;Benzi, Alice;Bianchi, Lara;Maccagno, Massimo;Pagano, Angela;Tavani, Cinzia;
2020-01-01
Abstract
The nitrovinyl moiety is surely one of the most reactive fragments in organic chemistry, continuously employed to explore original pathways and reach new targets. The short review herein represents an update on the potentialities in synthesis of conjugated mononitro or dinitro-1,3-butadienes: in such building blocks, the electrophilicity of the nitrovinyl moiety couples and takes advantage from the presence of a second, conjugated, vinyl moiety, most often leading to the eventual formation of diverse and/or diversely-functionalized heterocycles. The review will thus first of all provide chemists with recent, original protocols to such an important class of organic compounds as heterocycles, materials of choice for a lot of practical applications in different fields of human life.File | Dimensione | Formato | |
---|---|---|---|
R40-TeLe2020.pdf
accesso chiuso
Descrizione: Articolo principale
Tipologia:
Documento in versione editoriale
Dimensione
4.06 MB
Formato
Adobe PDF
|
4.06 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.