Asymmetric organocatalysis: an enabling technology for medicinal chemistry

B Han, XH He, YQ Liu, G He, C Peng… - Chemical Society Reviews, 2021 - pubs.rsc.org
The efficacy and synthetic versatility of asymmetric organocatalysis have contributed
enormously to the field of organic synthesis since the early 2000s. As asymmetric …

Medicinal chemistry of indole derivatives: Current to future therapeutic prospectives

A Kumari, RK Singh - Bioorganic chemistry, 2019 - Elsevier
Indole is a versatile pharmacophore, a privileged scaffold and an outstanding heterocyclic
compound with wide ranges of pharmacological activities due to different mechanisms of …

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

N Chadha, O Silakari - European Journal of Medicinal Chemistry, 2017 - Elsevier
Indoles constitute extensively explored heterocyclic ring systems with wide range of
applications in pathophysiological conditions that is, cancer, microbial and viral infections …

Isatin derivatives and their anti-bacterial activities

H Guo - European Journal of Medicinal Chemistry, 2019 - Elsevier
Bacterial infections are account for the majority of hospital-acquired and community-
acquired infections. The emergency and widespread of drug-resistant pathogens has further …

Recent developments and biological activities of thiazolidinone derivatives: A review

AK Jain, A Vaidya, V Ravichandran, SK Kashaw… - Bioorganic & medicinal …, 2012 - Elsevier
Thiazolidinone is considered as a biologically important active scaffold that possesses
almost all types of biological activities. Successful introduction of ralitoline as a potent anti …

Synthetic approaches, structure activity relationship and biological applications for pharmacologically attractive pyrazole/pyrazoline–thiazolidine-based hybrids

D Havrylyuk, O Roman, R Lesyk - European journal of medicinal chemistry, 2016 - Elsevier
The features of the chemistry of 4-thiazolidinone and pyrazole/pyrazolines as
pharmacologically attractive scaffolds were described in a number of reviews in which the …

Design, synthesis, molecular modeling, and antimicrobial potential of novel 3‐[(1H‐pyrazol‐3‐yl)imino]indolin‐2‐one derivatives as DNA gyrase inhibitors

AY Alzahrani, YA Ammar, MA Salem… - Archiv der …, 2022 - Wiley Online Library
Abstract A series of 3‐[(1H‐pyrazol‐3‐yl) imino] indolin‐2‐one derivatives were designed
using the molecular hybridization method, characterized using different spectroscopic …

Catalytic functionalization of tertiary alcohols to fully substituted carbon centres

L Chen, XP Yin, CH Wang, J Zhou - Organic & Biomolecular Chemistry, 2014 - pubs.rsc.org
The catalytic nucleophilic substitution of tertiary alcohols using carbon or heteroatom based
nucleophiles is a versatile methodology for the efficient, diverse and atom economical …

Indole clubbed 2, 4‐thiazolidinedione linked 1, 2, 3‐triazole as a potent antimalarial and antibacterial agent against drug‐resistant strain and molecular modeling …

DB Upadhyay, JA Mokariya, PJ Patel… - Archiv der …, 2024 - Wiley Online Library
In the face of escalating challenges of microbial resistance strains, this study describes the
design and synthesis of 5‐({1‐[(1H‐1, 2, 3‐triazol‐4‐yl) methyl]‐1H‐indol‐3‐yl} methylene) …

Spirooxindoles as Potential Pharmacophores.

SS Panda, RA Jones, P Bachawala… - Mini reviews in …, 2017 - europepmc.org
Objective The spirooxindole heterocyclic scaffold is found in many natural products and has
been identified as an important bioactive agent. Background Over the past few decades …