Your browser doesn't support javascript.
loading
Tricyclic 2-benzazepines obtained via an unexpected cyclization involving nitrilium ylides.
Inyutina, Anna; Dar'in, Dmitry; Kantin, Grigory; Krasavin, Mikhail.
Afiliação
  • Inyutina A; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.
  • Dar'in D; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.
  • Kantin G; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.
  • Krasavin M; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation. m.krasavin@spbu.ru d.dariin@spbu.ru.
Org Biomol Chem ; 19(23): 5068-5071, 2021 06 16.
Article em En | MEDLINE | ID: mdl-34027962
Attempted use of (E)-3-arylidene-4-diazopyrrolidine-2,5-diones in the Rh(ii)-catalyzed condensation with nitriles to form 1,3-oxazoles led to an unexpected outcome. The nitrilium ylide species thought to form on Rh(ii)-catalyzed decomposition of diazo compounds underwent a cyclization onto the nearby arylidene moiety followed by 1,5-hydride shift. This led to the formation of a 2-benzazepine core which has special significance for drug discovery and can be considered a privileged scaffold.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article