Synthesis and antifungal activity of (Z)-5-arylidenerhodanines

M Sortino, P Delgado, S Juárez, J Quiroga… - Bioorganic & Medicinal …, 2007 - Elsevier
An efficient microwave-assisted synthesis of new (Z)-5-arylidenerhodanines under solvent-
free conditions is described and their in vitro antifungal activity was evaluated following the …

Diversity-oriented catalyst-free synthesis of pseudopeptides containing rhodanine scaffolds via a one-pot sequential isocyanide-based six-component reactions in …

A Shaabani, SE Hooshmand - Ultrasonics Sonochemistry, 2018 - Elsevier
A planning strategy for diversity‐oriented catalyst-free synthesis of pseudopeptides
containing rhodanine scaffolds has been developed via a novel one-pot sequential six …

Urea/thiourea catalyzed, solvent-free synthesis of 5-arylidenethiazolidine-2, 4-diones and 5-arylidene-2-thioxothiazolidin-4-ones

S Shah, B Singh - Bioorganic & medicinal chemistry letters, 2012 - Elsevier
An efficient and organo-catalyzed method has been developed for the synthesis of 5-
arylidenethiazolidine-2, 4-diones and 5-arylidene-2-thioxothiazolidin-4-ones via …

Solvent‐free one‐pot synthesis of 2, 2′‐dithioxo‐[5, 5′] bithiazolidinylidene‐4, 4′‐diones

F Nasiri, A Zolali, S Asadbegi - Journal of Heterocyclic …, 2016 - Wiley Online Library
Solvent‐free One‐pot Synthesis of 2,2′‐dithioxo‐[5,5′]bithiazolidinylidene‐4,4′‐diones
- Nasiri - 2016 - Journal of Heterocyclic Chemistry - Wiley Online Library Skip to Article …

One-pot three-component route for the synthesis of rhodanine derivatives in water

AZ Halimehjani, S Hosseinkhany - Synthesis, 2015 - thieme-connect.com
A one-pot three-component route for the synthesis of rhodanine derivatives by the reaction
of primary amines, carbon disulfide, and maleic anhydride in water is described. The …

A novel multicomponent method for the synthesis of 2-thioxo-1, 3-thiazolidin-4-ones

A Alizadeh, N Zohreh - Synlett, 2009 - thieme-connect.com
Thieme E-Journals - Synlett / Full Text DE EN Home Products Journals Books Book Series
Service Library Service Help Contact Portal SYNLETT Full-text search Full-text search Author …

Fungicide Activity of 5‐(4‐Chlorobenzylidene)‐(Z)‐2‐dimethylamino‐1,3‐thiazol‐4‐one against Cryptococcus Neoformans

B Insuasty, A Gutiérrez, J Quiroga… - … der Pharmazie: An …, 2010 - Wiley Online Library
The present work describes the synthesis and antifungal evaluation of new 5‐arylidene‐(Z)‐
2‐dimethylamino‐1, 3‐thiazol‐4‐ones 4a–f, obtained by the reaction of aromatic aldehydes …

[PDF][PDF] Synthesis and structures of some new thiazolidin-4-ones and thiazolin-4-ones of anticipated biological activity

KA Kandeel - Arkivoc, 2006 - arkat-usa.org
Abstract The condensation of ω-(4-formylphenoxy) acetophenone (3a) and its 4-bromo
derivative (3b) with 2-thioxo-1, 3-thiazolidin-4-one (4a) and 1, 3-thiazolidin-2, 4-dione (4b) in …

Synthesis of phthalimido or succinimido-[2-aryl-4-oxo-3-[{2-oxo-2-(phenothiazin-10-yl) ethyl} amino]-1, 3-thiazolidin-5-yl] ethanoate and their antimicrobial activities

VK Salvi, S Sharma, C Sharma, D Bhambi, GL Talesara - 2009 - nopr.niscpr.res.in
Keeping in view the pharmacological potential of thiazolidinones and phenothiazines, the
title compounds containing these nuclei have been synthesized. Reaction of 10 …

Facile and convenient synthesis of 5-Arylalkylidenerhodanines by Electrocatalytic crossed Aldol condensation

H Veisi, Z Vafajoo, B Maleki… - Phosphorus, Sulfur, and …, 2013 - Taylor & Francis
An electrochemically induced catalytic crossed Aldol condensation of one equivalent of
rhodanine with various aromatic aldehydes and ketones in ethanol in an undivided cell in …