An overview of quinazolines: Pharmacological significance and recent developments

V Alagarsamy, K Chitra, G Saravanan… - European journal of …, 2018 - Elsevier
Most of the drugs and pharmacologically relevant molecules possess heterocyclic ring
structures and presence of hetero atoms or groupings divulges privileged specificities in …

Recent advances in synthesis of quinazoline‐2,4(1H,3H)‐diones: Versatile building blocks in N‐heterocyclic compounds

D Gheidari, M Mehrdad, S Maleki - Applied Organometallic …, 2022 - Wiley Online Library
Abstract Quinazoline‐2, 4 (1H, 3H)‐dione is a significant class of N‐fused heterocyclic with a
wide range of biological functions, including anti‐HIV, anticancer, antifungal, antibacterial …

Optimization of 2-anilino 4-amino substituted quinazolines into potent antimalarial agents with oral in vivo activity

PR Gilson, C Tan, KE Jarman, KN Lowes… - Journal of medicinal …, 2017 - ACS Publications
Novel antimalarial therapeutics that target multiple stages of the parasite lifecycle are
urgently required to tackle the emerging problem of resistance with current drugs. Here, we …

Discovery of novel quinazolines as potential anti-tubulin agents occupying three zones of colchicine domain

W Li, Y Yin, W Shuai, F Xu, H Yao, J Liu, K Cheng… - Bioorganic …, 2019 - Elsevier
A series of novel quinazolines as tubulin inhibitors occupying three zones of colchicine
domain have been designed and synthesized inspired by the recently disclosed crystal …

Metal-Free N–H/C–H Carbonylation by Phenyl Isocyanate: Divergent Synthesis of Six-Membered N-Heterocycles

K Govindan, A Jayaram, T Duraisamy… - The Journal of …, 2022 - ACS Publications
We disclose a method using phenyl isocyanate to synthesize carbonyl-containing N-
heterocycles. The metal-free novel approach for both N–H and C–H carbonylation …

NHC-catalyzed [12+ 2] reaction of polycyclic arylaldehydes for access to indole derivatives

H Ji, J Zou, C Mou, Y Liu, SC Ren… - Chemical Communications, 2023 - pubs.rsc.org
An N-heterocyclic carbene (NHC) catalyzed enantio-and diastereoselective [12+ 2]
cycloaddition is disclosed to rapidly construct sophisticated molecules bearing a tricyclic …

The quinazoline-2, 4 (1H, 3H)-diones skeleton: A key intermediate in drug synthesis

D Gheidari, M Mehrdad, S Maleki - Sustainable Chemistry and Pharmacy, 2022 - Elsevier
Abstract Quinazoline-2, 4 (1H, 3H)-dione is a major class of N-fused heterocyclic with a wide
range of biological functions, including anti-HIV, anticancer, antifungal, antibacterial …

DABCO-catalyzed one-pot three component synthesis of dihydropyrano [3, 2-c] chromene substituted quinazolines and their evaluation towards anticancer activity

S Vodnala, AKD Bhavani, R Kamutam… - Bioorganic & Medicinal …, 2016 - Elsevier
A facile DABCO promoted one-pot three component synthesis of a new series of C–C linked
bis-heterocycle containing dihydropyrano [c] chromene as highly fused oxa-heteryl group at …

Mechanism Exploration of Arylpiperazine Derivatives Targeting the 5-HT2A Receptor by In Silico Methods

F Lin, F Li, C Wang, J Wang, Y Yang, L Yang, Y Li - Molecules, 2017 - mdpi.com
As a G-protein coupled receptor, the 5-hydroxytryptamine 2A (5-HT2A) receptor is known for
its critical role in the cognitive, behavioural and physiological functions, and thus is a primary …

[HTML][HTML] Regioselective Nucleophilic Aromatic Substitution: Theoretical and Experimental Insights into 4-Aminoquinazoline Synthesis as a Privileged Structure in …

MLC Barbosa, PSM Pinheiro, R Alves da Conceição… - Molecules, 2024 - mdpi.com
The 4-aminoquinazoline scaffold is a privileged structure in medicinal chemistry.
Regioselective nucleophilic aromatic substitution (SNAr) for replacing the chlorine atom at …