From a synthetic perspective, bis (indolyl) methanes have undergone extensive
investigation over the past two to three decades owing to their remarkable pharmacological …

The five membered heteroaromatic oxazole motifs and their scaffolds exhibit significant
pharmaceutical and biological applications. Remarkably, the high efficiency in the assembly …

A metal-free one-pot method is established for the synthesis of tetrasubstituted imidazoles
from the reaction of arylmethylamines and 1, 2-dicarbonyls/benzoin. The N-α-C (sp3)–H …

Background: The bis (indolyl) methanes (BIMs) scaffold is reported for wide varieties of
pharmacological profiles, including antibacterial, anti-proliferative, anticancer, cytotoxic …

The indole moiety is an important N‐heterocycle found in natural products, and a key
structural component of many value‐added chemicals including pharmaceuticals. In …

The development of novel synthetic protocols for organic transformations is a key challenge
in fine chemical synthesis. A novel light-assisted protocol for the synthesis of bis (indolyl) …

A rapid practical process has been developed for synthesis of 2, 4, 5-trisubstituted-
imidazoles in excellent yields up to 95% from readily available starting materials. In this CuI …

A one-pot eco-friendly oxidative N-α-C (sp 3)–H bond functionalisation of arylmethylamines
for the synthesis of tetrasubstituted imidazoles is demonstrated. The substrate scope of …

Carbocatalysis represents a highly attractive and effective field within the realm of metal‐free
nanocatalysis, significantly advancing sustainability in synthetic chemistry. Graphene acid …

An environmentally benign synthesis of 3, 3'-bis (indolyl) methanes (BIMs) has been
developed from arylmethylamines and indoles under aerobic condition in presence of …