Chemistry and biological activities of 1, 3-thiazolidin-4-ones
1, 3-Thiazolidin-4-ones are an important group of heterocyclic compounds that are used in
the field of medicinal chemistry. The utility of 1, 3-thiazolidin-4-ones as synthons for various …
the field of medicinal chemistry. The utility of 1, 3-thiazolidin-4-ones as synthons for various …
Microwave-assisted Synthesis of Bioactive Six-membered O-heterocycles
Microwave radiation has been utilised since the late 1970s as an alternative thermal energy
source for chemical reactions. Initially used in inorganic chemistry, its potential for organic …
source for chemical reactions. Initially used in inorganic chemistry, its potential for organic …
2-Aryl-3-(2-morpholinoethyl) thiazolidin-4-ones: Synthesis, anti-inflammatory in vivo, cytotoxicity in vitro and molecular docking studies
DP Gouvea, FA Vasconcellos… - European journal of …, 2016 - Elsevier
Seven new 4-thiazolidinones bearing the morpholino moiety were easily synthesized by one-
pot reactions of 4-(2-aminoethyl) morpholine (2-morpholinoethylamine), arenealdehydes …
pot reactions of 4-(2-aminoethyl) morpholine (2-morpholinoethylamine), arenealdehydes …
[HTML][HTML] Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa (thia) zoles
Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa(thia)zoles -
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …
[HTML][HTML] Microwave assisted green synthesis of thiazolidin-4-one derivatives: A perspective on potent antiviral and antimicrobial activities
N Saini, A Sharma, VK Thakur, C Makatsoris… - Current Research in …, 2020 - Elsevier
Thiazolidin-4-one has been known as a powerful moiety present in various approved
medications. Thiazolidin-4-ones are amongst the most effective and actively explored fields …
medications. Thiazolidin-4-ones are amongst the most effective and actively explored fields …
Synthesis, antifungal and cytotoxic activities of 2-aryl-3-((piperidin-1-yl) ethyl) thiazolidinones
A Kunzler, PD Neuenfeldt, AM das Neves… - European journal of …, 2013 - Elsevier
A series of sixteen novel thiazolidinone derivatives were synthesized from the efficient one-
pot reaction of 2-(piperidin-1-yl) ethylamine, arenealdehydes and mercaptoacetic acid in …
pot reaction of 2-(piperidin-1-yl) ethylamine, arenealdehydes and mercaptoacetic acid in …
Efficient solvent-free synthesis of thiazolidin-4-ones from phenylhydrazine and 2, 4-dinitrophenylhydrazine
PD Neuenfeldt, BB Drawanz, GM Siqueira… - Tetrahedron …, 2010 - Elsevier
An efficient solvent-free synthesis of thiazolidinones from reaction of mercaptoacetic acid,
aldehydes (benzaldehyde and valeraldehyde) or ketones (cyclopentanone and …
aldehydes (benzaldehyde and valeraldehyde) or ketones (cyclopentanone and …
[HTML][HTML] Ultrasonics promoted synthesis of thiazolidinones from 2-aminopyridine and 2-picolilamine
DP Gouvêa, VDO Bareño, J Bosenbecker… - Ultrasonics …, 2012 - Elsevier
The efficient multicomponent synthesis of thiazolidinones from the reaction of
arenealdehydes, mercaptoacetic acid and 2-picolilamine or 2-aminopyridine under …
arenealdehydes, mercaptoacetic acid and 2-picolilamine or 2-aminopyridine under …
[HTML][HTML] Efficient sonochemical synthesis of thiazolidinones from piperonilamine
PD Neuenfeldt, AR Duval, BB Drawanz… - Ultrasonics …, 2011 - Elsevier
An efficient multicomponent reaction of arenealdehydes, mercaptoacetic acid and
piperonilamine under ultrasound irradiation to afford 2-aryl-3-(piperonylmethyl)-1, 3 …
piperonilamine under ultrasound irradiation to afford 2-aryl-3-(piperonylmethyl)-1, 3 …
Synthesis and docking studies of pyrazine–thiazolidinone hybrid scaffold targeting dormant tuberculosis
The persistence of Mycobacterium tuberculosis (MTB) in dormant stage assists the pathogen
to develop resistance against current antimycobactrial drugs. To address this issue, we …
to develop resistance against current antimycobactrial drugs. To address this issue, we …