Indium Trichloride-Catalyzed Imino Diels-Alder Reactions: Synthesis of New Indolylquinoline Derivatives
作者:Govindarajulu Babu、Rajagopal Nagarajan、Ramalingam Natarajan、Paramasivan T. Perumal
DOI:10.1055/s-2000-6387
日期:——
Imino Diels-Alder reaction of N-arylaldimines with cyclopentadiene, 3,4-dihydro-2H-pyran and indene is efficiently catalyzed by indium trichloride to give new indolylquinoline derivatives in good yields.
Indium trichloride (InCl3)catalyzed imino Diels-Alder reactions: An efficient synthesis of cyclopentaquinolines, azabicyclooctanones and azabicyclononanones
作者:Govindarajulu Babu、Paramasivan T. Perumal
DOI:10.1016/s0040-4020(97)10370-2
日期:1998.2
Anhydrous indiumtrichloride (InCl3) is found to catalyze the imino Diels-Alderreactions of Schiff's bases with cyclopentadiene, cyclohexen-2-one and cyclohepten-2-one which resulted in facile synthesis of cyclopentaquinolines, azabicyclooctanones and previously unreported series of azabicyclononanones.
Imino Diels-Alder reactions catalyzed by indium trichloride (InCl3). Facile synthesis of quinoline and phenanthridinone derivatives
作者:Govindarajulu Babu、Paramasivan T. Perumal
DOI:10.1016/s0040-4039(97)01060-5
日期:1997.7
Anhydrous indiumtrichloride (InCl3) is found to catalyze the imino Diels-Alderreactions and results in facile synthesis of quinoline derivatives. A previously unreported series of phenanthridinones was obtained by the treatment of cyclohexenones with Schiff bases.