A planning strategy for diversity‐oriented catalyst-free synthesis of pseudopeptides containing rhodanine scaffolds has been developed via a novel one-pot sequential six …
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 …
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 …
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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 …
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 …
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 …
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 …