138716-17-3Relevant articles and documents
A one-pot sequential five-component domino reaction for the expedient synthesis of polysubstituted pyrroles
Ambethkar, Sethurajan,Padmini, Vediappen,Bhuvanesh, Nattamai
, p. 4705 - 4709 (2016)
A series of novel pyrrole derivatives has been synthesized from readily available acetophenone, N,N-dimethylformamide dimethyl acetal, aniline, arylglyoxal and malononitrile in methanol under reflux conditions. This one-pot reaction constitutes a new and
Pd-catalyzed site selective C-H acetoxylation of aryl/heteroaryl/thiophenyl tethered dihydroquinolinones
Patpi, Santhosh Reddy,Sridhar, Balasubramanian,Tadikamalla, Prabhakar Rao,Kantevari, Srinivas
, p. 10251 - 10261 (2013/09/02)
Described herein is an efficient protocol for the site selective oxidative C-H activation/acetoxylation of a series of 2-aryl/heteroaryl/thiophenyl tethered dihydroquinolinones using palladium acetate as the catalyst and iodobenzene diacetate as an oxidan
Synthesis and antitubercular evaluation of novel substituted aryl and thiophenyl tethered dihydro-6H-quinolin-5-ones
Kantevari, Srinivas,Patpi, Santhosh Reddy,Sridhar, Balasubramanian,Yogeeswari, Perumal,Sriram, Dharmarajan
scheme or table, p. 1214 - 1217 (2011/04/16)
A series of novel aryl and thiophenyl tethered dihydro-6H-quinolin-5-ones have been synthesized in very good yields through CeCl3· 7H2O-NaI catalyzed one-pot condensation of β-enaminones derived from the respective methyl ketones; 1,
