25558-09-2Relevant articles and documents
Synthesis of novel tetrahydroindeno[1,2-b ]pyrrolidines via Ugi multicomponent and palladium-catalyzed aerobic oxidative cyclization
Ibarra-Rivera, Tannya R.,Rentería-Gómez, Manuel Alejandro,Nieto-Sepúlveda, Eduardo,Gámez-Monta?o, Rocío,Galindo, Verónica M. Rivas,Hernandez-Fernandez, Eugenio
, p. 509 - 515 (2016)
Novel tetrahydroindeno[1,2-b]pyrrolidines were conveniently prepared in moderate to good yields via a sequential Ugi multicomponent reaction or Staudinger/aza-Wittig/Ugi combination, followed by the palladium-catalyzed aerobic oxidative cyclization of the
A CONVENIENT SYNTHETIC METHOD FOR SCHIFF BASES. THE TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE-CATALYZED REACTION OF N,N-BIS(TRIMETHYLSILYL)AMINES WITH ALDEHYDES AND KETONES
Morimoto, Toshiaki,Sekiya, Minoru
, p. 1371 - 1372 (2007/10/02)
N,N-Bis(trimethylsilyl)amines react with aldehydes or ketones in the presence of trimethylsilyl trifluoromethanesulfonate to give Schiff bases in high yields.In situ utilization of the reaction solution as the Schiff base is also demonstrated.