Asymmetric organocatalysis is now an established methodology for the preparation of chiral compounds. However, these are not the only valuable molecules which can be conveniently obtained. Organocatalytic reactions affording achiral compounds are gaining momentum, opening unexplored pathways in the synthesis of densely functionalized aromatic moieties, olefins and useful molecules such as natural substances.

Non-asymmetric organocatalysis / Renzi, Polyssena; Bella, Marco. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 48:55(2012), pp. 6881-6896. [10.1039/c2cc31599h]

Non-asymmetric organocatalysis

RENZI, POLYSSENA;BELLA, Marco
2012

Abstract

Asymmetric organocatalysis is now an established methodology for the preparation of chiral compounds. However, these are not the only valuable molecules which can be conveniently obtained. Organocatalytic reactions affording achiral compounds are gaining momentum, opening unexplored pathways in the synthesis of densely functionalized aromatic moieties, olefins and useful molecules such as natural substances.
2012
(e)-alpha; stereoselective-synthesis; click-chemistry; nucleophilic carbenes; pull dienamine platform; n-heterocyclic carbene; organocatalysis; beta-unsaturated esters; medicinal chemistry; biological-activity; beta-unsaturated aldehydes; alpha; alpha-methylenation
01 Pubblicazione su rivista::01a Articolo in rivista
Non-asymmetric organocatalysis / Renzi, Polyssena; Bella, Marco. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 48:55(2012), pp. 6881-6896. [10.1039/c2cc31599h]
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/493007
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 5
  • Scopus 53
  • ???jsp.display-item.citation.isi??? 54
social impact