Microwave-assisted synthesis of quinazolines and quinazolinones: an overview

L Mohammadkhani, MM Heravi - Frontiers in chemistry, 2020 - frontiersin.org
Microwave irradiation (MWI), as a unique, effective, sustainable, more economic, and
greener source of energy compared to conventional heating, is applied in different organic …

Recent investigations in the synthesis of spirooxindole derivatives by Iranian researchers

L Youseftabar-Miri, H Hosseinjani-Pirdehi… - Journal of the Iranian …, 2020 - Springer
Among isatin-based heterocyclic, spirooxindoles are interesting synthetic molecules
because of their variety of pharmacological activities. There is a wide range of multi …

Design, synthesis, antimicrobial evaluation, and molecular docking study of some 4-thiazolidinone derivatives containing pyridine and quinazoline moiety

NC Desai, KA Jadeja, DJ Jadeja… - Synthetic …, 2021 - Taylor & Francis
Abstract A series of 5-aryl-3-(4-oxo-2-phenylquinazolin-3 (4 H)-yl)-2-(pyridin-4-yl) thiazolidin-
4-ones were synthesized and evaluated for their antibacterial and antifungal activities …

Design, synthesis and docking studies of some spiro-oxindole dihydroquinazolinones as antibacterial agents

J Zhang, J Zhao, L Wang, J Liu, D Ren, Y Ma - Tetrahedron, 2016 - Elsevier
Two series of spiro-oxindole dihydroquinazolinone derivatives have been designed and
synthesized using a catalytic amount of nano cerium oxide with excellent product yields by a …

Design and synthesis of a new series of hybrids of functionalised N1-[(1H-1, 2, 3-triazol-4-yl) methyl] quinazoline-2, 4-dione with antiviral activity against Respiratory …

IE Głowacka, K Gawron, DG Piotrowska, M Graus… - Antiviral Research, 2023 - Elsevier
In this study, a series of 48 hybrids of the functionalised 1-[(1H-1, 2, 3-triazole-4-yl) methyl]
quinazoline-2, 4-dione 17–22 were synthesised and evaluated for potential antiviral activity …

Facile synthesis of new quinazolinone benzamides as potent tyrosinase inhibitors: Comparative spectroscopic and molecular docking studies

PG Mahajan, NC Dige, BD Vanjare, H Raza… - Journal of Molecular …, 2019 - Elsevier
The simple reaction approach has been designed and utilized for the synthesis of
quinazolinone benzamides 4a-4h using isatoic anhydride, m-Anisic hydrazide and various …

2-Aminoethanesulfonic acid: An efficient organocatalyst for green synthesis of spirooxindole dihydroquinazolinones and novel 1,2-(dihydroquinazolin-3(4H) …

AV Chate, PP Rudrawar, GM Bondle… - Synthetic …, 2020 - Taylor & Francis
A facile and efficient one-pot procedure for the preparation of spirooxindole
dihydroquinazolinone derivatives and new N-(4-oxo-2-phenyl-1, 2-dihydroquinazolin-3 (4 …

[HTML][HTML] Efficient Synthesis of 2-Aminoquinazoline Derivatives via Acid-Mediated [4+2] Annulation of N-Benzyl Cyanamides

ZY Qin, CX Sun, WW Zhang, JR Li, YX Gong, WM Shu… - Catalysts, 2023 - mdpi.com
The synthesis of 2-aminoquinazoline derivatives is achieved by using hydrochloric acid as a
mediator in the [4+ 2] annulation reaction between N-benzyl cyanamides and 2-amino aryl …

An efficient approach for the synthesis of new (±)-coixspirolactams

VR Nascimento, MLS Suenaga… - Organic & Biomolecular …, 2020 - pubs.rsc.org
Coixspirolactams, spiro [oxindole-γ-lactones], are found in adlay seeds and exhibit
anticancer activity. A novel synthetic methodology was developed to enable an easy access …

Synthesis, characterization, molecular docking studies and biological evaluation of some novel hybrids based on quinazolinone, benzofuran and imidazolium …

P Asadi, G Khodarahmi… - Iranian journal of …, 2017 - pmc.ncbi.nlm.nih.gov
Objective (s): Hybridization of bioactive natural and synthetic compounds is one of the most
promising novel approaches for the design of hit and lead compounds with new molecular …