17282-95-0Relevant articles and documents
Unexpected simultaneous synthesis of trisubstituted quinolines and acylhydrazones under catalyst-free conditions
Hosseyni Largani, Tahere,Imanzadeh, Gholamhassan,Noroozi Pesyan, Nader,?ahin, Ertan
supporting information, p. 1077 - 1084 (2017/05/25)
Trisubstituted quinolines and acylhydrazones were unexpectedly prepared from a reaction of N′-((2-aminophenyl)(phenyl)methylene)benzohydrazides with acetylenic esters. Using of N′-((2-aminophenyl)(phenyl)methylene)benzohydrazides led to obtain not only qu
Recyclable nano copper oxide catalyzed synthesis of quinoline-2,3- dicarboxylates under ligand free conditions
Venkanna, Avudoddi,Swapna, Kokkirala,Rao, Pallapothula Venkateswar
, p. 15154 - 15160 (2014/04/17)
An efficient protocol was developed for the recyclable nano CuO powder catalyzed synthesis of quinoline derivatives from acetylenedicarboxylates and 2-aminocarbonyl compounds using acetonitrile as solvent at 40 °C in air. A variety of quinoline derivatives were synthesized in good yields with good chemoselectivity in the presence of a catalytic amount of CuO nano powder under ligand/additive free conditions. The catalyst is air-stable, inexpensive and recyclable up to four cycles. the Partner Organisations 2014.
Copper(ii) triflate-catalyzed reactions for the synthesis of novel and diverse quinoline carboxylates
Pandit, Rameshwar Prasad,Lee, Yong Rok
, p. 22039 - 22045 (2013/11/06)
An efficient one-pot synthesis of a variety of quinoline carboxylates was accomplished by Cu(OTf)2-catalyzed reactions of Michael addition/cyclization/aromatization between 2-aminoaryl carbonyls and alkynyl carboxylates. This methodology offers
