128404-93-3Relevant academic research and scientific papers
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.
REACTION OF MERCAPTOACETIC ACID AND CHLOROACETYL CHLORIDE WITH BENZALAMINO THIAZOLYL COUMARINS
Veerabhadraiah, Udarapu,Rajeswar Rao, Vedeela,Padmanabha Rao, Tadepalcy Venkata
, p. 535 - 539 (2007/10/02)
2-Aryl-3--4-thiazolidinones (III), have been synthesized by the reaction of Schiff's bases (II) derived from 3-(2-amino-4-thiazolyl)-2H-1-benzopyran-2-ones (I) with mercaptoacetic acid.The Schiff's bases on reaction with chloroacetyl chloride in the presence of triethylamine in dioxane gave chloroacetamido derivative (IV) instead of expected compound V.
