Atropisomers are compounds in which chirality arises from hindered rotation along the carbon–carbon or carbon–heteroatom single bond. Recently, organocatalysis appeared to be a rapid, valuable, and efficient strategy for their preparation in an enantioselective manner. In this report a general overview of the most important organocatalyzed atroposelective transformations will be given pointing out in particular the specific role played by the catalyst.

Organocatalytic Strategies for the Synthesis of Axially Chiral Compounds / Bencivenni, G.. - In: SYNLETT. - ISSN 0936-5214. - STAMPA. - 26:14(2015), pp. 1915-1922. [10.1055/s-0034-1378712]

Organocatalytic Strategies for the Synthesis of Axially Chiral Compounds

BENCIVENNI, GIORGIO
2015

Abstract

Atropisomers are compounds in which chirality arises from hindered rotation along the carbon–carbon or carbon–heteroatom single bond. Recently, organocatalysis appeared to be a rapid, valuable, and efficient strategy for their preparation in an enantioselective manner. In this report a general overview of the most important organocatalyzed atroposelective transformations will be given pointing out in particular the specific role played by the catalyst.
2015
Organocatalytic Strategies for the Synthesis of Axially Chiral Compounds / Bencivenni, G.. - In: SYNLETT. - ISSN 0936-5214. - STAMPA. - 26:14(2015), pp. 1915-1922. [10.1055/s-0034-1378712]
Bencivenni, G.
File in questo prodotto:
File Dimensione Formato  
s-0034-1378712.pdf

accesso riservato

Tipo: Versione (PDF) editoriale
Licenza: Licenza per accesso riservato
Dimensione 386.34 kB
Formato Adobe PDF
386.34 kB Adobe PDF   Visualizza/Apri   Contatta l'autore
Synpacts_revised.pdf

accesso aperto

Tipo: Postprint
Licenza: Licenza per accesso libero gratuito
Dimensione 865.76 kB
Formato Adobe PDF
865.76 kB Adobe PDF Visualizza/Apri

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/11585/515425
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 83
  • ???jsp.display-item.citation.isi??? 81
social impact