A palladium-catalyzed ortho-C− H amidation of anilides by N-nosyloxycarbamates was
developed for the synthesis of 2-aminoanilines. This reaction can be carried out under …

The use of bismuth (III) salts in organic synthesis has attracted an increasing interest over
the last years. Systems comprising of bismuth (III) salts are generally catalytic and involve a …

There are some 850 human G protein-coupled receptors (GPCRs) currently known
(http://bioinformatics2. biol. uoa. gr), making this the most abundant family of well …

4-Hydroxyphenylpyruvate dioxygenase (HPPD, EC 1.13. 11.27) is one of the most valuable
herbicide targets due to its unique biological functions. In search of HPPD inhibitors with …

Inhibitors of the PI3-kinase/AKT (protein kinase B) pathway are under investigation as
anticancer and antiviral agents. The benzimidazole derivative AKT inhibitor-IV (ChemBridge …

The desulfurization ability of diacetoxyiodobenzene (DIB) has been explored in the
preparation of isothiocyanates from the corresponding dithiocarbamate salts. The in situ …

Rh (III)-catalyzed aromatic C–H amination of acetophenone o-methyloximes with primary N-
chloroalkylamines was developed, and the arylamine products were obtained in up to 92 …

Molecules | Free Full-Text | An Effective Microwave-Induced Iodine-Catalyzed Method for the
Synthesis of Quinoxalines via Condensation of 1,2-Diamines with 1,2-Dicarbonyl Compounds …

A new class of benzimidazole derivatives as tubulin polymerization inhibitors has been
designed and synthesized in this study. The in vitro anticancer profile of the developed …

A new series of carboxamide-bearing benzimidazole derivatives have been reported for
their cytotoxicity profile (in vitro) on selected human tumour cells like A549, HCT116, SK-Mel …