823213-16-7Relevant academic research and scientific papers
3-(5-(Benzylideneamino)thiazol-3-yl)-2H-chromen-2-ones: A new class of alkaline phosphatase and ecto-5′-nucleotidase inhibitors
Saeed, Aamer,Ejaz, Syeda Abida,Shehzad, Muddasar,Hassan, Sidra,Al-Rashida, Mariya,Lecka, Joanna,Sévigny, Jean,Iqbal, Jamshed
, p. 21026 - 21036 (2016/03/05)
A new series of 3-(2-(benzylideneamino)thiazol-4-yl)-2H-chromen-2-ones has been synthesized. The structures of the compounds were established by means of 1H and 13C NMR spectroscopy. All compounds were evaluated for their potential t
Novel approach for the rapid and efficient synthesis of heterocyclic Schiff bases and azetidinones under microwave irradiation
Naik, Bhanvesh,Desai
, p. 267 - 271 (2007/10/03)
A series of compounds, viz. 3″-chloro-4″-(substituted phenyl)-1″-[4-(coumarin-3-yl)thiazol-2-yl]-2″-azetidinones 4a-j have been prepared by the reaction of 2-N-(substituted benzylidene)imino-4- (coumarin-3-yl)lhiazoles 3a-j with chloroacetyl chloride in m
Synthesis and evaluation of anticancer and antiviral activity of some 2-aryl-3-(4-(2H-1-benzopyran-2-one-3-yl)-2-thiazolyl)-5-methyl-4-thiazolidinones
Rajeswar Rao,Vijaya Kumar,Ravinder Reddy,Reddy
, p. 273 - 284 (2007/10/03)
2-Aryl-3-(4-(2H-1-benzopyran-2-one-3-yl)-2-thiazolyl)-5-methyl-4- thiazolidinones (3), have been prepared by the reaction of Schiff's bases (2) with 2-mercaptopropionic acid. The Schiffs bases in turn are obtained by the reaction of various aldehydes with 3-(2-amino-4-thiazolyl)coumarins. The compounds 3 have been evaluated for their anticancer and antiviral activity.
