References

10.1002/9780470742761

10.1002/9780470742761 · ExternalCitation · doi-reference

N-heterocyclic carbene catalyzed intramolecular hydroacylation of activated alkynes: Synthesis of chromones

10.1002/adsc.201000828 · ExternalCitation · doi-reference

Transition-metal-free C(sp2)–H dithiocarbamation and chromone annulation cascade for 3-dithiocarbamyl chromone synthesis

10.1002/adsc.202100617 · ExternalCitation · doi-reference

C3-functionalized chromones synthesis by tandem C–H elaboration and chromone annulation of enaminones

10.1002/ajoc.201900196 · ExternalCitation · doi-reference

Metal-free, facile synthesis of sulfenylated chromones and indoles promoted by an aqueous HBr–DMSO system

10.1002/ajoc.201900402 · ExternalCitation · doi-reference

Transition-metal-free intramolecular Ullmann-type O-arylation: Synthesis of chromone derivatives

10.1002/ange.201007302 · ExternalCitation · doi-reference

Cobalt-catalyzed annulation of salicylaldehydes and alkynes to form chromones and 4-chromanones

10.1002/anie.201510999 · ExternalCitation · doi-reference

Novel 5h-chromeno [4, 3-b] pyridin-5-one derivatives against phytopathogenic fungi: Synthesis and molecular docking

10.1002/cbdv.202500386 · ExternalCitation · doi-reference

Styrylchromones: Biological activities and structure-activity relationship

10.1002/cmdc.202400782 · ExternalCitation · doi-reference

Revolutionizing anti-fungal strategies: novel Chromone-based microtubulin target fungicides for Sclerotinia sclerotiorum of oilseed rape

10.1002/ps.70666 · ExternalCitation · doi-reference

Synthesis, leishmanicidal, trypanocidal and cytotoxic activities of quinoline-chalcone and quinoline-chromone hybrids

10.1007/s00044-017-1846-5 · ExternalCitation · doi-reference

Synthesis and evaluation of chromone-2-carboxamido-alkylamines as potent acetylcholinesterase inhibitors

10.1007/s00044-020-02508-5 · ExternalCitation · doi-reference

Ion channels: molecular targets of neuroactive insecticides

10.1007/s10158-005-0004-9 · ExternalCitation · doi-reference

Synthesis and evaluation of chromone derivatives as inhibitors of monoamine oxidase

10.1007/s11030-019-09917-8 · ExternalCitation · doi-reference

Current strategies in development of new chromone derivatives with diversified pharmacological activities: A review

10.1007/s11094-020-02187-x · ExternalCitation · doi-reference

Identification of a diarylpentanoid-producing polyketide synthase in the biosynthesis of 2-(2-phenylethyl)chromones in agarwood

10.1007/s11418-023-01743-5 · ExternalCitation · doi-reference

A novel synthesis of chromone based unnatural α-amino acid derivatives

10.1007/s12039-017-1328-9 · ExternalCitation · doi-reference

Structure-antioxidant activity relationships of flavonoids and phenolic acids

10.1016/0891-5849(95)02227-9 · ExternalCitation · doi-reference

Synthesis of 4-hydroxy-1-methylindole and benzo [b] thiophen-4-ol based unnatural flavonoids as new class of antimicrobial agents

10.1016/j.bmc.2004.12.032 · ExternalCitation · doi-reference

Synthesis and insecticidal activity of chromanone and chromone analogues of diacylhydrazines

10.1016/j.bmc.2007.01.008 · ExternalCitation · doi-reference

Rearranged limonoids and chromones from Harrisonia perforata and their anti-inflammatory activity

10.1016/j.bmcl.2013.04.064 · ExternalCitation · doi-reference

Synthesis, biological evaluation and molecular docking studies of chromone hydrazone derivatives as α-glucosidase inhibitors

10.1016/j.bmcl.2017.05.007 · ExternalCitation · doi-reference

Design, synthesis and anti-TMV activities of novel chromone derivatives containing dithioacetal moiety

10.1016/j.bmcl.2019.126945 · ExternalCitation · doi-reference

Synthesis, characterization and antioxidant activity of chitosan-chromone derivatives

10.1016/j.carbpol.2017.11.074 · ExternalCitation · doi-reference

Synthesis, nematicidal activity and docking study of novel chromone derivatives containing substituted pyrazole

10.1016/j.cclet.2017.10.011 · ExternalCitation · doi-reference

2-(phenyl)-4H-chromen-4-ones: Green synthesis, characterization, in vitro antifungal evaluation and molecular docking approach toward Aspergillus fumigatus

10.1016/j.crgsc.2021.100234 · ExternalCitation · doi-reference

Mechanism of unusual formation of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl) chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides and their antimicrobial evaluation

10.1016/j.ejmech.2009.03.030 · ExternalCitation · doi-reference

Synthesis and evaluation of novel chromone analogs for their inhibitory activity against interleukin-5

10.1016/j.ejmech.2010.02.041 · ExternalCitation · doi-reference

Chromones as a privileged scaffold in drug discovery: A review

10.1016/j.ejmech.2014.03.047 · ExternalCitation · doi-reference

Novel chromone and xanthone derivatives: Synthesis and ROS/RNS scavenging activities

10.1016/j.ejmech.2016.03.043 · ExternalCitation · doi-reference

Design and synthesis of chromone-based monoamine oxidase B inhibitors with improved drug-like properties

10.1016/j.ejmech.2022.114507 · ExternalCitation · doi-reference

Evaluation of anti-nociceptive, anti-inflammatory and antipyretic activities of Artemisia scoparia hydromethanolic extract

10.1016/j.jep.2012.10.022 · ExternalCitation · doi-reference

Artemisia leaf extract induces apoptosis in human endometriotic cells through regulation of the p38 and NFκB pathways

10.1016/j.jep.2012.12.003 · ExternalCitation · doi-reference

Design and synthesis of some chromone derivatives of biological importance: A greener approach

10.1016/j.matpr.2017.09.109 · ExternalCitation · doi-reference

Synthesis, biological evaluation and molecular docking studies of chromone derivatives as potential α-glucosidase inhibitors

10.1016/j.molstruc.2022.134575 · ExternalCitation · doi-reference

Chromone derivatives from Halenia elliptica and their anti-HBV activities

10.1016/j.phytochem.2011.09.015 · ExternalCitation · doi-reference

Synthesis of functionalized chromones via organocatalysis

10.1016/j.tet.2014.10.045 · ExternalCitation · doi-reference

Divergent synthesis of chromones and chromanones from diketones using an AgOTf/[Si]H system by switching hydrosilanes

10.1016/j.tet.2024.134087 · ExternalCitation · doi-reference

Electrophilic carbon transfer in gold catalysis: Synthesis of substituted chromones

10.1016/j.tetlet.2011.03.018 · ExternalCitation · doi-reference

Advances in flavonoid research since 1992

10.1016/s0031-9422(00)00235-1 · ExternalCitation · doi-reference

2 Chromone-2-and-3-carboxylic acids and their derivatives

10.1016/s0079-6468(08)70397-7 · ExternalCitation · doi-reference

Insecticidal structure and bioactivities of compounds from Ficus sarmentosa var. henryi

10.1016/s1671-2927(11)60133-8 · ExternalCitation · doi-reference

Discovery of novel chromone derivatives containing a sulfonamide moiety as anti-ToCV agents through the tomato chlorosis virus coat protein-oriented screening method

10.1021/acs.jafc.1c02467 · ExternalCitation · doi-reference

Discovery of novel chromone derivatives as potential anti-TSWV agents

10.1021/acs.jafc.1c03626 · ExternalCitation · doi-reference

Recent advances and outlook of benzopyran derivatives in the discovery of agricultural chemicals

10.1021/acs.jafc.3c09244 · ExternalCitation · doi-reference

Insect antifeedant potential of xanthohumol, isoxanthohumol, and their derivatives

10.1021/acs.jafc.5b02025 · ExternalCitation · doi-reference

A novel chromone-sulfonyl hydrazone scaffold targeting fungal tubulin: design, synthesis, and antifungal mechanism against Sclerotinia sclerotiorum

10.1021/acs.jafc.5c10776 · ExternalCitation · doi-reference

Synthesis and antifungal activity of chromones and benzoxepines from the leaves of Ptaeroxylon obliquum

10.1021/acs.jnatprod.0c00587 · ExternalCitation · doi-reference

Biflorin, isolated from the flower buds of Syzygium aromaticum L, suppresses LPS-induced inflammatory mediators via STAT1 inactivation in macrophages and protects mice from endotoxin shock

10.1021/acs.jnatprod.5b00609 · ExternalCitation · doi-reference

Cascade in situ iodination, chromone annulation, and cyanation for site-selective synthesis of 2-cyanochromones

10.1021/acs.joc.3c00206 · ExternalCitation · doi-reference

Synthesis of succinimide-containing chromones, naphthoquinones, and xanthones under Rh(III) catalysis: Evaluation of anticancer activity

10.1021/acs.joc.6b02577 · ExternalCitation · doi-reference

Synthesis of chromones from 1,1-diacylcyclopropanes: Toward the synthesis of bromophycoic acid e

10.1021/acs.joc.7b00648 · ExternalCitation · doi-reference

On-water Cp\ Ir(III)-catalyzed C–H functionalization for the synthesis of chromones through annulation of salicylaldehydes with diazo-ketones

10.1021/acs.joc.9b00418 · ExternalCitation · doi-reference

Cp\ Ir(III)-catalyzed C–H/O–H functionalization of salicylaldehydes for the synthesis of chromones at room temperature

10.1021/acs.joc.9b01139 · ExternalCitation · doi-reference

Divergent synthesis of 2-chromonyl-3-hydrazono-chromones and 2-alkoxy-3-hydrazono-chromones through switchable annulation reactions of o-hydroxyphenylenaminones with aryldiazonium salts

10.1021/acs.orglett.4c01571 · ExternalCitation · doi-reference

Green method for the synthesis of chromeno[2,3-c]pyrazol-4(1H)-ones through ionic liquid promoted directed annulation of 5-(aryloxy)-1H-pyrazole-4-carbaldehydes in aqueous media

10.1021/acs.orglett.5b00033 · ExternalCitation · doi-reference

De novo construction of highly substituted chromones and benzo [b] furans via a switchable transformation of 3-alkynyl-4-pyrones with active methylene compounds

10.1021/acs.orglett.5c02822 · ExternalCitation · doi-reference

Controllable Rh(III)-catalyzed annulation between salicylaldehydes and diazo compounds: Divergent synthesis of chromones and benzofurans

10.1021/acs.orglett.6b03355 · ExternalCitation · doi-reference

Thermoinduced free-radical C–H acyloxylation of tertiary enaminones: Catalyst-free synthesis of acyloxyl chromones and enaminones

10.1021/acs.orglett.8b01536 · ExternalCitation · doi-reference

Synthesis and antifungal activity of novel imidazole derivatives

10.1021/acsagscitech.4c00622 · ExternalCitation · doi-reference

Design, synthesis and biological evaluation of chromeno [3, 4-b] xanthones as multifunctional agents for alzheimer’s disease

10.1021/acschemneuro.5c00425 · ExternalCitation · doi-reference

Biological and medicinal properties of natural chromones and chromanones

10.1021/acsomega.4c00771 · ExternalCitation · doi-reference

Chromone: a valid scaffold in medicinal chemistry

10.1021/cr400265z · ExternalCitation · doi-reference

Insect antifeedant activity of flavones and chromones against Spodoptera litura

10.1021/jf025627a · ExternalCitation · doi-reference

Design, synthesis, and biological evaluation of chromone-based p38 MAP kinase inhibitors

10.1021/jm200818j · ExternalCitation · doi-reference

Synthesis and evaluation of substituted chroman-4-one and chromone derivatives as sirtuin 2-selective inhibitors

10.1021/jm3005288 · ExternalCitation · doi-reference

New frontiers in selective human MAO-B inhibitors: Miniperspective

10.1021/jm501690r · ExternalCitation · doi-reference

Synthesis of chromones via palladium-catalyzed ligand-free cyclocarbonylation of o-iodophenols with terminal acetylenes in phosphonium salt ionic liquids

10.1021/jo902210p · ExternalCitation · doi-reference

Antioxidant lignans and chromone glycosides from Eurya japonica

10.1021/np3007638 · ExternalCitation · doi-reference

2-Phenoxychromones and prenylflavonoids from Epimedium koreanum and their inhibitory effects on LPS-induced nitric oxide and interleukin-1β production

10.1021/np400831p · ExternalCitation · doi-reference

K2CO3-catalyzed synthesis of chromones and 4-quinolones through the cleavage of aromatic C–O bonds

10.1021/ol300908g · ExternalCitation · doi-reference

Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood

10.1038/s41467-022-27971-z · ExternalCitation · doi-reference

New hybrid hydrazinyl thiazole substituted chromones: As potential α-amylase inhibitors and radical (DPPH & ABTS) scavengers

10.1038/s41598-017-17261-w · ExternalCitation · doi-reference

Synthesis, bioactivity assessment, molecular docking and ADMET studies of new chromone congeners exhibiting potent anticancer activity

10.1038/s41598-024-59606-2 · ExternalCitation · doi-reference

Synthesis, biological evaluation, and molecular docking of novel coumarin-based bisimine derivatives

10.1038/s41598-025-26301-9 · ExternalCitation · doi-reference

Synthesis, SAR, and in silico studies of new benzochromene derivatives as insecticidal agents against Culex pipiens L larvae and adults

10.1038/s41598-025-30027-z · ExternalCitation · doi-reference

Novel benzofuran–chromone and coumarin derivatives: Synthesis and biological activity in K562 human leukemia cells

10.1039/c3md00241a · ExternalCitation · doi-reference

First intramolecular Diels–Alder reactions using chromone derivatives: Synthesis of chromeno[3,4-b]xanthones and 2-(benzo[c]chromenyl)chromones

10.1039/c7nj05185a · ExternalCitation · doi-reference

Iodine-mediated synthesis of sulfur-bridged enaminones and chromones via double C(sp2)–H thiolation

10.1039/c7ob00619e · ExternalCitation · doi-reference

Synthesis of chiral chromanols via a RuPHOX–Ru catalyzed asymmetric hydrogenation of chromones

10.1039/c8cc07787h · ExternalCitation · doi-reference

PIDA-mediated α-C–H functionalization of enaminones: The synthesis of thiocyano enaminones and chromones in water

10.1039/c9nj04580e · ExternalCitation · doi-reference

Rh(III)-catalyzed C–H activation/annulation of salicylaldehydes with sulfoxonium ylides for the synthesis of chromones

10.1039/c9qo00830f · ExternalCitation · doi-reference

Toward C2-nitrogenated chromones by copper-catalyzed β-C(sp2)–H N-heteroarylation of enaminones

10.1039/d0qo00065e · ExternalCitation · doi-reference

Cytotoxic dihydrothiophene-condensed chromones from the marine-derived fungus Penicillium oxalicum

10.1055/s-0033-1350805 · ExternalCitation · doi-reference

Electrochemically induced thiocyanation of enaminones: Synthesis of functionalized alkenes and chromones

10.1055/s-0039-1691486 · ExternalCitation · doi-reference

Convenient one-pot synthesis of chromone derivatives and their antifungal and antibacterial evaluation

10.1080/00397911.2011.647222 · ExternalCitation · doi-reference

Ion channels as insecticide targets

10.1080/01677063.2016.1229781 · ExternalCitation · doi-reference

New chromone analog and pyrrole alkaloid produced by Penicillium sclerotiorum and their antibacterial activity

10.1080/10286020.2022.2084585 · ExternalCitation · doi-reference

Structure and biological activity of a new rotenoid from Pongamia pinnata

10.1080/10575630290033114 · ExternalCitation · doi-reference

New secondary metabolites from bioactive extracts of the fungus Armillaria tabescens

10.1080/14786419.2012.738206 · ExternalCitation · doi-reference

A new chromone from the twig of Mallotus apelta

10.1080/14786419.2014.951853 · ExternalCitation · doi-reference

A new potent immunosuppressive isoflavanonol from Campylotropis hirtella

10.1080/14786419.2015.1063053 · ExternalCitation · doi-reference

Pharmaceutical methods for enhancing the dissolution of poorly water-soluble drugs

10.1089/adt.2022.119 · ExternalCitation · doi-reference

Flavonoids: A review of probable mechanisms of action and potential applications

10.1093/ajcn/74.4.418 · ExternalCitation · doi-reference

Antifungal and antibiofilm activities of chromones against nine Candida species

10.1128/spectrum.01737-23 · ExternalCitation · doi-reference

Microwave-assisted synthesis, molecular docking, and insecticidal activity of 1,2,3-triazole-linked chromone derivatives

10.1134/s1070363224010169 · ExternalCitation · doi-reference

Design, synthesis, and biological evaluation of novel 4-chromanone-derived compounds incorporating an oxime ether moiety

10.1134/s1070363225601760 · ExternalCitation · doi-reference

Antifungal activity of some new flavones and flavone glycosides of Echinops echinatus

10.1139/b88-260 · ExternalCitation · doi-reference

Synthesis and evaluation of some novel chromone based dithiazoles as antimicrobial agents

10.1155/2013/815453 · ExternalCitation · doi-reference

New chromone and triglyceride from Cucumis melo seeds

10.1177/1934578x1400900217 · ExternalCitation · doi-reference

Isoflavonoids from Crotalaria albida inhibit adipocyte differentiation and lipid accumulation in 3T3-L1 cells via suppression of PPAR-γ pathway

10.1371/journal.pone.0135893 · ExternalCitation · doi-reference

Flavonoids of Lonchocarpus montanus AMG Azevedo and biological activity

10.1590/s0001-37652007000300001 · ExternalCitation · doi-reference

Isolation, identification, and insecticidal activity of chromone compounds from Trichoderma harzianum against Aedes aegypti larvae

10.16801/j.issn.1008-7303.2025.0046 · ExternalCitation · doi-reference

Synthesis and herbicidal activity of heterocyclic azlactone and imidazolinone derivatives

10.21608/asejaiqjsae.2015.2957 · ExternalCitation · doi-reference

A comprehensive guide to the development, evaluation, and future prospects of self-nanoemulsifying drug delivery systems for poorly water-soluble drugs

10.2174/0113816128296705240327065131 · ExternalCitation · doi-reference

Nanotechnology in drug delivery: Overcoming poor solubility challenges through nanoformulations

10.2174/0124681873276732231207051324 · ExternalCitation · doi-reference

Recent advances in the catalytic one-pot synthesis of flavonoids and chromones

10.2174/1389557517666170315124951 · ExternalCitation · doi-reference

An efficient synthesis of novel chromone-containing furopyrimidines

10.3184/174751911x13146322603355 · ExternalCitation · doi-reference

Synthesis, biological evaluation and QSAR studies of 3-iodochromone derivatives as potential fungicides

10.3389/fchem.2021.636882 · ExternalCitation · doi-reference

Novel indazolylchromones: synthesis, fungicidal evaluation, molecular docking and aquatic toxicity prediction

10.3389/fchem.2024.1411187 · ExternalCitation · doi-reference

Naturally occurring chromone glycosides: Sources, bioactivities, and spectroscopic features

10.3390/molecules26247646 · ExternalCitation · doi-reference

Synthesis and antimicrobial evaluation of chroman-4-one and homoisoflavonoid derivatives

10.3390/molecules30173575 · ExternalCitation · doi-reference

Enhancing the bioavailability of poorly soluble drugs

10.3390/pharmaceutics16060758 · ExternalCitation · doi-reference

Antifungal activity of 4′,7-dimethoxyisoflavone against some fungi

10.4489/myco.2002.30.1.055 · ExternalCitation · doi-reference

Synthesis and anti-bacterial activity of 1, 4-dihydropyridine derivatives embedded with chromone and dimedone based hybrids

10.5958/0974-4150.2018.00012.3 · ExternalCitation · doi-reference