Torsional angles in 6,6?-bridged atropoisomeric biphenyls control the electrophilic substitution with phthalimidesulfenyl chlorid (Articolo in rivista)

Type

• Articolo in rivista (Classe)
• Prodotto della ricerca (Classe)

Label

• Torsional angles in 6,6?-bridged atropoisomeric biphenyls control the electrophilic substitution with phthalimidesulfenyl chlorid (Articolo in rivista) (literal)

Anno

• 2003-01-01T00:00:00+01:00 (literal)

Alternative label

• Delogu, G.; Fabbri, D.; Menichetti, S.; Nativi, C. (2003)
  Torsional angles in 6,6?-bridged atropoisomeric biphenyls control the electrophilic substitution with phthalimidesulfenyl chlorid
  
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Delogu, G.; Fabbri, D.; Menichetti, S.; Nativi, C. (literal)

Pagina inizio

• 2131 (literal)

Pagina fine

• 2136 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume

• 59 (literal)

Note

• ISI Web of Science (WOS) (literal)

Titolo

• Torsional angles in 6,6?-bridged atropoisomeric biphenyls control the electrophilic substitution with phthalimidesulfenyl chlorid (literal)

Abstract

• The reaction of phthalimidesulfenyl chloride with 2,2',6,6'-hydroxylated biphenyls allowed the preparation of 3- and/or 3,3'-N-thiophthalimide derivatives which can be easily transformed into the corresponding thiols and/or disulfides. Mono- or bis-substitution, as well as the regiochemistry of the sulfenylation, are predictable as a function of the substituents on the biphenyl unit and the lenght of the 6,6'bridge. (literal)

Prodotto di

• Institute of biomolecular chemistry (ICB) (Istituto)

Autore CNR

• GIOVANNA MARIA DELOGU (Persona)
• DAVIDE GAETANO FABBRI (Unità di personale interno)

Incoming links:

Autore CNR di

• DAVIDE GAETANO FABBRI (Unità di personale interno)
• GIOVANNA MARIA DELOGU (Persona)

Prodotto

• Institute of biomolecular chemistry (ICB) (Istituto)