Many studies have been focused on the selective separation of hydrogen chloride (HCl)
gas, but its capture and conversion in situ is still at a standstill. Herein, a pioneering attempt …

Rates and selectivities for liquid-phase reactions depend on the structure and acidity of
active sites within zeolite catalysts and the solvent environment surrounding the active sites …

A salen-based Ce-MOFs contained rich uncoordinated imine (− CH= N−) groups (termed as
N-Ce-salen) has been synthesized by using solution-diffusion method. Furthermore, the as …

This study explored the catalytic performance of two robust zirconium-based metal–organic
frameworks (MOFs), MIP-202 (Zr) and UiO-66-(CO2H) 2 in the ring-opening of epoxides …

Adding an amine moiety to a carbonyl group poses a challenging synthetic task;
nevertheless, it is a crucial step in developing numerous bioactive molecules. Here, we …

Herein, we introduce a mild and efficient method for synthesizing aniline biaryls and
unsymmetrical phenol biaryls through iodine-catalyzed coupling of quinone imine ketals …

SnCl2 catalyzed three-component coupling of aniline, epoxide, and paraformaldehyde
resulted in the synthesis of 1, 3-oxazolidine derivatives. The reaction is simple and does not …

Using commercially available Pd/C as a catalyst, β-amino alcohols are synthesized from
nitroarenes and 1, 2-epoxides. Nitroarenes are transformed to amines through ring opening …

We report a straightforward, metal-free, efficient protocol for the synthesis of 2-
phenylnaphthalenes from 1-phenylethane-1, 2-diols under mild conditions. In this strategy …

One significant and elegant method for creating β-amino alcohols, which are useful
intermediates for the synthesis of many different natural and synthetic pharmaceutical …