Abstract
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Takahiro Yamada, Rinka Fujita, Ayaka Kishino, Norihiko Takeda, Masafumi Ueda
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
unpaywall
Confidence 95%
datacite
Confidence 0%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Natural and synthetic chromenes, fused chromenes, and versatility of dihydrobenzo[h]chromenes in organic synthesis
10.1021/cr500075s · 2014
Coumarin: A natural, privileged and versatile scaffold for bioactive compounds
10.3390/molecules23020250 · 2018
An overview of coumarin as a versatile and readily accessible scaffold with broad-ranging biological activities
10.3390/ijms21134618 · 2020
Recent advances of coumarin-type compounds in discovery of pesticides
10.1021/acs.jafc.4c06538 · 2024
Coumarins and coumarin-related compounds in pharmacotherapy of cancer
10.3390/cancers12071959 · 2020
Recent advances and therapeutic journey of coumarins: current status and perspectives
10.1007/s00044-015-1350-8 · 2015
Coumarin-based small-molecule fluorescent chemosensors
10.1021/acs.chemrev.9b00145 · 2019
Synthesis and application of coumarin fluorescence probes
10.1039/c9ra10290f · 2020
Review of recent advancements in fluorescent chemosensor for ion detection via coumarin derivatives
10.1007/s11696-022-02092-5 · 2022
π-Expanded coumarins: synthesis, optical properties and applications
10.1039/c4tc02665a · 2015
Substitution effects on the optoelectronic properties of coumarin derivatives
10.3390/app10010144 · 2019
Therapeutic effects of coumarins with different substitution patterns
10.3390/molecules28052413 · 2023
Exotines A and B, two heterodimers of isopentenyl-substituted indole and coumarin derivatives from Murraya exotica
10.1021/acs.orglett.5b02230 · 2015
Cancer chemopreventive agents, 4-phenylcoumarins from Calophyllum inophyllum
10.1016/s0304-3835(01)00521-3 · 2001
Antimalarial 4-phenylcoumarins from the stem bark of Hintonia Latiflora
10.1021/np060233p · 2006
Synthesis and biological evaluation of 4-arylcoumarin analogues of combretastatins Part 2
10.1021/jm901826e · 2011
Secondary metabolites from endophytic Streptomyces aureofaciens CMUAc130 and their antifungal activity
10.1099/mic.0.27758-0 · 2005
Specific inhibition of human immunodeficiency virus type 1 reverse transcriptase mediated by Soulattrolide, a coumarin isolated from the latex of Calophyllum teysmannii
10.1021/np960399y · 1996
Synthesis and antiprotozoal activity of 4-arylcoumarins
10.1016/j.ejmech.2009.10.022 · 2010
Recent advances and perspectives in the synthesis of bioactive coumarins
10.1039/c6ra07071j · 2016
Recent advances in the synthesis of coumarin derivatives from different starting materials
10.3390/biom10010151 · 2020
Recent advances in the design and synthesis of coumarins and their derivatives via Suzuki–Miyaura reaction (2002–2024)
10.1007/s00706-025-03396-4 · 2025
Derivatization of coumarins at the benzenoid ring in aqueous medium
10.1002/jhet.1800 · 2014
Discovery of an NF-κB1 P105 degrader for anti-inflammatory therapy via structural optimization of the coumarin natural product Minutuminolate
10.1021/acs.jmedchem.5c00055 · 2025
Site-selective C-H bond functionalization of chromones and coumarins
10.1002/ajoc.201800128 · 2018
Coumarins synthesis and transformation via C–H bond activation—a review
10.3390/inorganics10020023 · 2022
A facile route to flavone and neoflavone backbones via a regioselective palladium catalyzed oxidative heck reaction
10.1039/c2cc18150a · 2012
Palladium-catalyzed oxidative heck coupling reaction for direct synthesis of 4-arylcoumarins using coumarins and arylboronic acids
10.1021/jo202577m · 2012
Regioselective palladium—catalyzed olefination of coumarins via aerobic oxidative heck reactions
10.1039/c2cc37676h · 2012
Access to 4-alkenylated coumarins via ruthenium-catalyzed olefinic C–H alkenylation of coumarins with modifiable and removable directing groups
10.1021/acs.joc.0c00249 · 2020
Pd(II)-Catalyzed Fujiwara–Moritani reactions for the synthesis and functionalization of substituted coumarins
10.1021/acsomega.1c03469 · 2021
Regioselective palladium-catalyzed direct cross-coupling of coumarins with simple arenes
10.1039/c2cc34551j · 2012
Highly regioselective α-arylation of coumarins via palladium-catalyzed C–H activation/desulfitative coupling
10.1002/adsc.201300707 · 2013
Palladium-catalyzed carbonylation of coumarin C(sp2)–H bonds: a new entry to arylcoumarin ketones
10.1055/s-0037-1610675 · 2018
Visible light-induced cross-dehydrocoupling of 3-cyanocoumarins with unactivated aliphatic aldehydes enables access to 4-acylated coumarins
10.1021/acs.joc.2c02928 · 2023
Regioselective palladium-catalyzed phosphonation of coumarins with dialkyl H-phosphonates via C–H functionalization
10.1021/ol4031167 · 2013
Palladium catalyzed C–I and vicinal C–H dual activation of diaryliodonium salts for diarylation: synthesis of 4,5-benzocoumarins
10.1021/acs.orglett.5b02938 · 2015
Polar-effect-directed control in site-selectivity of radical substitution enables C–H perfluoroalkylation of coumarins
10.1021/acs.joc.4c01469 · 2024
Copper-catalyzed synthesis of difluoromethylated/C-4- and C-5-functionalized polycyclic coumarin derivatives
10.1021/acs.joc.4c00766 · 2024
Regiodivergent Pd-catalyzed annulation of coumarins: directing-group-controlled coumarin-fused N-heterocycles
10.1021/acs.orglett.6c00915 · 2026
Arene activation with mercury(II) and thallium(III) electrophiles. Mechanistic relevance of charge-transfer transitions in π-complexes as intermediates
10.1021/ja00281a043 · doi-reference
Thallium in organic synthesis. XXII. Electrophilic aromatic thallation using thallium(III) trifluoroacetate Simple synthesis of aromatic iodides
10.1021/ja00748a029 · doi-reference
4-Arylcoumarin inhibits immediate-type allergy
10.1080/09540100701788636 · doi-reference
Bioconjugation with strained alkenes and alkynes
10.1021/ar200059z · doi-reference
Rapid Cu-free click chemistry with readily synthesized biarylazacyclooctynones
10.1021/ja100014q · doi-reference
Aza-dibenzocyclooctynes for fast and efficient enzyme PEGylation via copper-free (3+2) cycloaddition
10.1039/b917797c · doi-reference
Fishing for drug targets: A focus on diazirine photoaffinity probe synthesis
10.1021/acs.jmedchem.7b01561 · doi-reference
Aliphatic diazirines as photoaffinity probes for proteins: recent developments
10.1021/cr1002722 · doi-reference
Palladium(II)-catalyzed oxidative coupling of arenes by thallium(III)
10.1016/s0040-4020(01)91964-7 · doi-reference
Synthesis of aromatic carbonyl compounds via thallation-carbonylation of arenes
10.1021/ja00371a019 · doi-reference
Palladium(II)-catalyzed oxidation of substituted benzenes to biaryls by tris(trifluoroacetato)thallium(III)
10.1016/s0040-4039(01)82023-2 · doi-reference
Biomimetically inspired, one-step synthesis of exotine A and exotine B
10.1021/acs.joc.0c01524 · doi-reference
Total synthesis of (±)–exotine B
10.1021/acs.orglett.8b01817 · doi-reference
Pd/Tl Bimetal-catalyzed C3(5)–H activation of pyridine derivatives enables access to pyridine-fused benzophospholes and their transformation into seven-membered phosphepines
10.1021/acs.orglett.5c05316 · doi-reference
Electrophilic C3–H alkenylation of 2,6-dialkoxypyridine derivatives via Pd(II)/Tl(III) reaction system
10.1002/adsc.202300650 · doi-reference
Bimetallic catalysis for C–C and C–X coupling reactions
10.1039/c6sc05556g · doi-reference
Heteromultimetallic catalysis for sustainable organic syntheses
10.1039/c6cs00787b · doi-reference
Synergistic dual transition metal catalysis
10.1021/acs.chemrev.0c00245 · doi-reference
Efficient activation of aromatic C–H bonds for addition to C–C multiple bonds
10.1126/science.287.5460.1992 · doi-reference
Oligothiophene synthesis by a general C–H activation mechanism: electrophilic concerted metalation–deprotonation (eCMD)
10.1021/acscatal.9b01195 · doi-reference
C–H Alkenylation of heteroarenes: mechanism, rate, and selectivity changes enabled by thioether ligands
10.1021/jacs.7b03887 · doi-reference
Benzenoid ring C–H olefination of coumarins under Rh(III)-catalysis: synthesis, anti-inflammatory evaluation and in silico studies
10.1016/j.bioorg.2026.109553 · doi-reference