Pyrrole derivatives comprise a class of biologically active heterocyclic compounds which
can serve as promising scaffolds for antimicrobial, antiviral, antimalarial, antitubercular, anti …

A series of indole and pyridine based 1, 3, 4-oxadiazole derivatives 5a–t were synthesized
and evaluated for their in vitro antitubercular activity against Mycobacterium tuberculosis H …

Due to the emergence of drug‐resistant microbial strains, different research groups are
continuously develo** novel drug molecules against already exploited and unexploited …

In search of more potent and safe new antitubercular agents, here new 2-pyridinyl
substituted thiazolyl-5-aryl-1, 3, 4-oxadiazoles (6a–o), have been designed and synthesized …

Cinnamic acid and its derivatives are known for anti-tubercular activity. The present study
reports the synthesis of cinnamic acid derivatives via bioisosteric replacement of terminal …

Microwave-assisted organic reaction enhancement (MORE) has become more important in
synthetic organic chemistry for efficient resource utilization. In this study, we synthesized …

ABSTRACT A series of pyridine clubbed 1, 3, 4-oxadiazole derivatives were efficiently
synthesized, characterized by standard spectral techniques and evaluated for their in vitro …

Cancer is one of the leading causes of deaths globally. Despite many anticancer agents in
the market, cancer stood as a major health concern to humanity due to the problems like …

Dihydropyrimidones substituted pyrrole were prepared in high yields from three-component
coupling of alkyl isocyanides, dialkyl acetylenedicarboxylates and dihydropyrimidone …

Abstract An analogue of novel 3‐(1‐(4‐(benzoyl) benzyl)‐1H‐indol‐5‐yl)‐1, 2, 4‐oxadiazol‐
5 (4H)‐ones were synthesized in good yields (80–90%), and its anti‐tubercular (anti‐TB) …