Introduction Hybrid drug design has developed as a prime method for the development of
novel anticancer therapies that can theoretically solve much of the pharmacokinetic …

It is well-known that thiazole derivatives are usually found in lead structures, which
demonstrate a wide range of pharmacological effects. The aim of this research was to …

Primary and secondary alcohols have been converted into 2-amino-1, 3-thiazoles under
microwave irradiation, employing trichloroisocyanuric acid (TCCA) as a dual oxidant and …

A direct single-pot three-component procedure for synthesizing bio-active hydrazinyl
thiazole derivatives has been demonstrated. The reaction involves substituted 2 …

4-Aryl-3-thiocyanatobutan-2-ones were prepared by Meerwein reactions from methyl vinyl
ketone and aryldiazonium salts under copper (II) catalysis in 35–75% yields. α-Thiocyanato …

In our preliminary in vitro studies, the Enhydra fluctuans extract demonstrated inhibition of
calcium phosphate (brushite) crystals. Human serum albumin (HSA) is known to act as a …

A simple and efficient one-pot protocol has been developed for the conversion of styrenes
into 4-aryl-2-aminothiazoles using readily available starting materials. Tribromoisocyanuric …

The current review aimed to provide an understanding of the preparation, reactions, and
biological action of thiazoles. The purpose of this review was to focus on the progress made …

Novel series of heterocycliccompounds pairing hybrids pyrazole, naphthalene and
pyrazoline/thiazoldinemoieties were synthesized. The starting compounds pyrazolyl …

Both one-pot and two-step procedures for the synthesis of substituted 2-aminothiazoles and
2-aminoselenazoles are described. Anilines are first converted into arenediazonium …