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Enantioselective Nickel-Catalyzed Intramolecular Allylic Alkenylations Enabled by Reversible Alkenylnickel E/Z Isomerization.
Yap, Connor; Lenagh-Snow, Gabriel M J; Karad, Somnath Narayan; Lewis, William; Diorazio, Louis J; Lam, Hon Wai.
Afiliación
  • Yap C; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
  • Lenagh-Snow GMJ; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Karad SN; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Lewis W; The GSK Carbon Neutral Laboratories for Sustainable Chemistry, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.
  • Diorazio LJ; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
  • Lam HW; School of Chemistry, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Angew Chem Int Ed Engl ; 56(28): 8216-8220, 2017 07 03.
Article en En | MEDLINE | ID: mdl-28544752
ABSTRACT
Enantioselective nickel-catalyzed arylative cyclizations of substrates containing a Z-allylic phosphate tethered to an alkyne are described. These reactions give multisubstituted chiral aza- and carbocycles, and are initiated by the addition of an arylboronic acid to the alkyne, followed by cyclization of the resulting alkenylnickel species onto the allylic phosphate. The reversible E/Z isomerization of the alkenylnickel species is essential for the success of the reactions.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2017 Tipo del documento: Article País de afiliación: Reino Unido