69199-99-1Relevant academic research and scientific papers
Synthesis, receptor affinity and effect on pentylenetetrazole-induced seizure threshold of novel benzodiazepine analogues: 3-Substituted 5-(2-phenoxybenzyl)-4H-1,2,4-triazoles and 2-amino-5-(phenoxybenzyl)-1,3,4- oxadiazoles
Mashayekh, Siavash,Rahmanipour, Narges,Mahmoodi, Behnaz,Ahmadi, Fatemeh,Motaharian, Dina,Shahhosseini, Soraya,Shafaroodi, Hamed,Banafshe, Hamid R.,Shafiee, Abbas,Navidpour, Latifeh
, p. 1929 - 1937 (2014)
The new series of 5-(2-phenoxybenzyl)-4H-1,2,4-triazoles, possessing C-3 thio, alkylthio and ethoxy substituents, and 2-amino-5-(2-phenoxybenzyl)-1,3,4- oxadiazoles were designed and synthesized as novel benzodiazepine analogues. Most of them revealed sim
Synthesis, conformational assignment, and anti-inflammatory activities of N-arylidene-2-(4-chloro-2-(2-substituted phenoxy)phenyl)acetic acid hydrazides
Nakhostin, Afraz,Mirseyyedhosein, Samaneh,Toolabi, Mahsa,Khodabakhsh, Pariya,Aghamiri, Helia,Ghaffari, Soheila,Shafaroodi, Hamed,Shayesteh, Alireza,Amini, Mohsen,Shafiee, Abbas,Navidpour, Latifeh
, p. 2220 - 2236 (2016/10/25)
A series of N-arylidene-2-(4-chloro-2-(2-fluoro or chlorophenoxy)phenyl)acetic acid hydrazides (16 or 17) was synthesized for their anti-inflammatory activity by the condensation of corresponding hydrazide and aromatic aldehydes. Characterization of these
Microwave-assisted synthesis of 2-phenoxybenzoic acids
Pellon, Rolando F.,Martin, Ana,Mesa, Miriam,Docampo, Maite L.,Gomez, Victoria
, p. 527 - 529 (2007/10/03)
Substituted 2-phenoxybenzoic acid derivatives were synthesised in high yield and in short reaction times using the Ullmann condensation of 2-chlorobenzoic acid with phenol derivatives under microwave irradiation in dry media.
The use of ultrasound in the synthesis of 2-carboxy substituted diphenylethers using water as solvent
Pellon Comdom, Rolando F.,Docampo Palacios, Maite L.
, p. 921 - 926 (2007/10/03)
An improved synthesis of 2-carboxy substituted diphenylethers using water as solvent can be achieved by ultrasound irradiation. A number of diphenylethers was prepared in good yields in a very short reaction time.
