Biological activity of oxadiazole and thiadiazole derivatives

UA Atmaram, SM Roopan - Applied Microbiology and Biotechnology, 2022 - Springer
The 5-membered oxadiazole and thiadiazole scaffolds are the most privileged and well-
known heterocycles, being a common and essential feature of a variety of natural products …

Recent advances of imidazole-containing derivatives as anti-tubercular agents

YL Fan, XH Jin, ZP Huang, HF Yu, ZG Zeng… - European journal of …, 2018 - Elsevier
Tuberculosis still remains one of the most common, communicable, and leading deadliest
diseases known to mankind throughout the world. Drug-resistance in Mycobacterium …

Anti-tuberculosis activity and its structure-activity relationship (SAR) studies of oxadiazole derivatives: A key review

SK Verma, R Verma, S Verma, Y Vaishnav… - European Journal of …, 2021 - Elsevier
With the increasing number of cases of inactive and drug-resistance tuberculosis, there is an
urgent need to develop new potent molecules set for fighting this brutal disease. Medicinal …

A panoramic review of benzimidazole derivatives and their potential biological activity

H Hernández-López… - Mini Reviews in …, 2022 - ingentaconnect.com
The therapeutic potential of the benzimidazole nucleus has been recognized since 1944,
and it is an important heterocycle system due to its presence in a wide range of bioactive …

The first one-pot ambient-temperature synthesis of 1, 2, 4-oxadiazoles from amidoximes and carboxylic acid esters

S Baykov, T Sharonova, A Shetnev, S Rozhkov… - Tetrahedron, 2017 - Elsevier
The first one-pot room-temperature protocol for the synthesis of 3, 5-disubstituted-1, 2, 4-
oxadiazoles via the condensation between amidoximes and carboxylic acid esters in …

Recent advancements and developments in search of anti-tuberculosis agents: a quinquennial update and future directions

TM Dhameliya, KA Bhakhar, ND Gajjar, KA Patel… - Journal of Molecular …, 2022 - Elsevier
Tuberculosis (TB) has been considered as the highly chronic, contagious and infectious
disorder caused by Mycobacterium tuberculosis (Mtb). Every year more than 10 million …

Exploration of Remarkably Potential Multitarget-Directed N-Alkylated-2-(substituted phenyl)-1H-benzimidazole Derivatives as Antiproliferative, Antifungal, and …

NKN Phan, TKC Huynh, HP Nguyen, QT Le… - ACS …, 2023 - ACS Publications
Improving lipophilicity for drugs to penetrate the lipid membrane and decreasing bacterial
and fungal coinfections for patients with cancer pose challenges in the drug development …

Oxadiazole scaffolds in anti-tuberculosis drug discovery

SS De, MP Khambete, MS Degani - Bioorganic & medicinal chemistry …, 2019 - Elsevier
With the increasing number of cases of latent and drug resistant tuberculosis, there is an
urgent need to develop new, potent molecules capable of combating this deadly disease …

Synthesis of 1,2-Fused/Disubstituted Benzimidazoles and Benzimidazolium Salts by I2-Mediated sp3 C–H Amination

X Yi, Z Zhao, M Wang, W Yu, J Chang - Organic Letters, 2022 - ACS Publications
An intramolecular sp3 C–H amination reaction of aniline derivatives has been established.
This reaction employs molecular iodine (I2) under transition-metal-free conditions and …

Electrochemical Synthesis of Benzo[d]imidazole via Intramolecular C(sp3)–H Amination

A Li, C Li, T Yang, Z Yang, Y Liu, LJ Li… - The Journal of …, 2021 - ACS Publications
An electrochemical dehydrogenative amination for the synthesis of benzimidazoles was
developed. This electrosynthesis method could address the limitations of the C (sp3)–H …