Mild and highly efficient method for the synthesis of arylidenethiazolidinone analogues was written by Chandrappa, S.;Vinaya, K.;Prasanna, D. S.;Rangappa, K. S.. And the article was included in Proceedings of the Indian National Science Academy in 2011.Category: thiazolidine This article mentions the following:
A new, convenient method for the syntheses of arylidenethiazolidinone analogs e. g., I from gem-dibromomethylarenes and 2,4-thiazolidindiones under mild conditions is described. Short reaction times, large-scale synthesis, easy and quick isolation of the products, and excellent yields are the main advantages of this method. In the experiment, the researchers used many compounds, for example, 3-Methylthiazolidine-2,4-dione (cas: 16312-21-3Category: thiazolidine).
3-Methylthiazolidine-2,4-dione (cas: 16312-21-3) belongs to thiazolidine derivatives. Thiazolidine is an important scaffold and has a wide range of promising biological activities. Thiazolidine derivatives have reported anti-inflammatory and anti-nociceptive activity. Thiazolidine and its composites are key components of many natural products and drugs , and are also present in many synthetic compounds such as anticancer, anti-inflammatory, antitubercular, antifungal, antiviral, anti-HIV, cytotoxicity, antitrypanosomal, antinociceptive and anti-hypernociceptive compounds.Category: thiazolidine
Referemce:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com