Chemical Communications Journal
The reaction of cyclic amides with acetylene under low pressure, using ruthenium-phosphine catalysts, afforded a broad variety of N-vinylated amides including (azabicyclic) lactams, oxazolidinones, benzoisoxazolones, isoindolinones, quinoxalinones, oxazinanones, cyclic urea derivatives (imidazolidinones), nucleobases (thymine), amino acid anhydrides and thiazolidinone.
For details: Ruthenium-catalyzed synthesis of vinylamides at low acetylene pressures
Elena Semina a, Pavel Tuzina b, Frank Bienewald b, A. Stephen K. Hashmi ac and Thomas Schaub ab
a Catalysis Research Laboratory (CaRLa) Im Neuenheimer Feld 584, 69120 Heidelberg, Germany
b Organic Synthesis, BASF SE Carl-Bosch-Str. 38, 67056 Ludwigshafen, Germany
c Organisch-Chemisches Institut, Heidelberg University Im Neuenheimer Feld 270, 69120 Heidelberg, Germany
For more information about Chemspeed solutions:
Chemical Communications Journal
https://doi.org/10.1039/D0CC01533D
This journal is © The Royal Society of Chemistry 2020
For details please contact [email protected]