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 …
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 …
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
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 …
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 …
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
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 …
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
Tuberculosis (TB) has been considered as the highly chronic, contagious and infectious
disorder caused by Mycobacterium tuberculosis (Mtb). Every year more than 10 million …
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 …
and fungal coinfections for patients with cancer pose challenges in the drug development …
Oxadiazole scaffolds in anti-tuberculosis drug discovery
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 …
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 …
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 …
developed. This electrosynthesis method could address the limitations of the C (sp3)–H …