Emergence of multidrug resistant and extensively drug resistant tuberculosis has prompted
to develop new molecular entities to treat the disease. A series of new 4‐thiazolidinones …

Compounds interacting with cell protein tubulin and microtubules represent an important
type of antimitotic agents. A series of tubulin-targeted 2-aryl-4-benzoyl-imidazoles were …

Abstract Novel 2-heteroaryl-N-[4-(substituted aryl) thiazol-2-yl] propanamide derivatives (7a–
7o) were synthesized and investigated for their antimicrobial activity. Among the tested …

A series of combretastatin A-4 analogs in which cis-olefinic bond replaced by thiazole ring
were prepared by reaction of α-bromo-1, 2-(p-substituted) diaryl-1-ethanones and …

A novel, facile reaction for the synthesis of series of bis‐thiazole derivatives has been
developed from the reaction of the appropriate thiosemicarbazone derivatives and bis‐2 …

Organic synthesis involves the production of important chemical structures using scalable
and cost‐effective methods that are also environmentally friendly. In this review, a detailed …

A three-step method was designed and developed on the basis of retrosynthetic analysis for
the synthesis of hybrid molecules containing a thiazole ring and an N-sulfonyl amidine …

A series of novel 1-thiazolyl-5-coumarin-3-yl-pyrazole derivatives (4a–l) were synthesized
via one-pot multicomponent reaction of 5-substituted salicylaldehydes (1a–c), 4-hydroxy-6 …

A simple, three-component synthesis of 2-aminothiazoles using trimethylsilyl isothiocyanate -
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Aim: Choline kinase α inhibitors represent one of the newest classes of cytotoxic drugs for
cancer treatment, since aberrant choline metabolism is a characteristic shared by many …