An overview of the preparation and synthetic potentialities of functionalized organoselenium and organotellurium compounds is presented. Various methods to generate selenated or tellurated nucleophiles are described. Focusing on the more recent developments, in this Perspective reactions of selenium and tellurium nucleophiles with heterocycles (O-, N-, and S-containing) of different ring size (three, four, five, and six-membered) to access a variety of organo-chalcogen compounds, bearing different functional groups, are covered. Their application in organic synthesis and asymmetric catalysis is also reported, along with some novel methodologies derived thereof.
Ring opening reactions of heterocycles with selenium and tellurium nucleophiles / Tanini, Damiano; Capperucci, Antonella. - In: NEW JOURNAL OF CHEMISTRY. - ISSN 1144-0546. - ELETTRONICO. - 43:(2019), pp. 11451-11468. [10.1039/C9NJ02320H]
Ring opening reactions of heterocycles with selenium and tellurium nucleophiles
Tanini, DamianoMembro del Collaboration Group
;Capperucci, Antonella
Membro del Collaboration Group
2019
Abstract
An overview of the preparation and synthetic potentialities of functionalized organoselenium and organotellurium compounds is presented. Various methods to generate selenated or tellurated nucleophiles are described. Focusing on the more recent developments, in this Perspective reactions of selenium and tellurium nucleophiles with heterocycles (O-, N-, and S-containing) of different ring size (three, four, five, and six-membered) to access a variety of organo-chalcogen compounds, bearing different functional groups, are covered. Their application in organic synthesis and asymmetric catalysis is also reported, along with some novel methodologies derived thereof.File | Dimensione | Formato | |
---|---|---|---|
NJC_2019_Perspective.pdf
accesso aperto
Descrizione: Articolo principale
Tipologia:
Altro
Licenza:
Tutti i diritti riservati
Dimensione
492.83 kB
Formato
Adobe PDF
|
492.83 kB | Adobe PDF |
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.