The hydrogenation of nitro compounds to their corresponding amines is developed using a
heterogeneous and recyclable catalyst (V2O5/TiO2) under irradiation of blue LED (9 W) at …

A simple and efficient method for preparation of 2‐amino‐3‐substituted quinazolin‐4 (3H)‐
ones by reaction of cyanuric chloride with 2‐amino N‐substituted benzamides in acetonitrile …

The potential of 2-aminoquinazolin-4 (3H)-one as an organocatalyst for the activation of
aldehydes via noncovalent interaction for the synthesis of tertiary amines using formic acid …

The transition metal free reduction of aromatic/heteroaromatic nitro compounds to amines
has been improved employing phenyl (2‐quinolyl) methanol (PQM) as organocatalyst in the …

Aromatic amines are important intermediates in the industry to produce a wide array of
products, and the reduction of aromatic nitro compounds is the main methodology for their …

2‐Aminoquinazolin‐4‐one based efficient organocatalytic eco‐friendly reductive amination
approach was developed for the mono N‐alkylation of anilines using hydrosilane as a …

Herein, a highly efficient, simple, base-free, chemoselective and environmentally-benign
strategy was developed for the reduction of nitro compounds using NaBH4 as a hydrogen …