the aryl-(z)-n-[2-amino-1,2-dicyanovinyl]formamidine 2 cyclize in solvent-free conditions and in the presence of a base to give a 5-amino-1-aryl-4-cyanoimidazoles 3. silica sulfuric acid as an efficient and reusable heterogeneous catalyst has been used for the preparation of amidines 2 from formimidate 1 through reaction with aromatic amines at room temperature and in good to excellent yields. ...

LC-MS/MS method to determine hydrophobic N-alkyloxy substituted amidines: N-(2-ethylhexyloxy)pyridine-2-carboximidamide, N-(2-ethylhexyloxy)pyridine-3-carboximidamide, N-(2-ethylhexyloxy)pyridine-4-carboximidamide, N-decyloxy pyridine-2-carboximidamide, N-decyloxypyridine-3-carboximidamide and N-decyloxypyridine-4-carboximidamide was developed and validated in terms of linearity, precision and ...

2-Aminobenzimidazole 10, although a weak catalyst in the monomeric state, is successful building block for effective artificial ribonucleases. In an effort to identify new blocks with improved catalytic potential, RNA cleavage by variety of heterocyclic amidines and guanidines has been studied. addition pKa values steric effects, energy difference between tautomeric forms seems be another impor...

In the field of organic chemistry, a base is generally defined as a reagent capable of abstracting proton to yield a carbanion species. At a basic textbook level, organobases are normally limited to amines, which are categorized as very weak bases according to the above definition. The introduction of an imine function (1⁄4NH) to the a-carbon of amines affords more basic amine species, amidines...

Lattices of single polystyrene particles were constructed by using a combinatorial approach to analyze particle pattern recognition properties. Dip-pen nanolithography was used to generate chemical templates of 16-thiohexadecanoic acid on a gold surface to study the two-dimensional assembly of amine- and amidine-modified particles.