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Dimeric Guaianolides and a Fulvenoguaianolide from Artemisia myriantha
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-9422(90)85432-fopenalex-snapshot
Guaianolides from Kaunia lasiophthalma
inferredcites →https://doi.org/10.1016/0031-9422(90)87129-iopenalex-snapshot
Guaianolides and other constituents from Artemisia douglasiana
inferredcites →https://doi.org/10.1016/0031-9422(91)80045-3openalex-snapshot
A sesquiterpene glucoside from Reichardia tingitana
inferredcites →https://doi.org/10.1016/s0031-9422(00)81853-1openalex-snapshot
Fulvene lactones from Tanacetum annuum
inferredcites →https://doi.org/10.1021/jo00141a020openalex-snapshot
Syntheses of arborescin, 1,10-epiarborescin, and (11S)-guaia-3,10(14)-dieno-13,6.alpha.-lactone, the key intermediate in Greene and Crabbe's estafiatin synthesis, and the stereochemical assignment of arborescin
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112955zenodo-depositor-declared
Guaianolides from Artemisia codonocephala suppress interleukine-1β secretion in macrophages
inferred← citeshttps://doi.org/10.1002/ardp.201100065openalex-snapshot
Synthesis and Biological Evaluation of Antitumor‐Active Arglabin Derivatives
inferred← citeshttps://doi.org/10.1002/cbdv.202502438openalex-snapshot
Four New Compounds From Lactuca indica That Inhibit Nitric Oxide Production
inferred← citeshttps://doi.org/10.1002/cjoc.202100528openalex-snapshot
Artematrovirenolides A—D and Artematrolides S—Z, Sesquiterpenoid Dimers with Cytotoxicity against Three Hepatoma Cell Lines from Artemisia atrovirens
inferred← citeshttps://doi.org/10.1002/ejoc.201301445openalex-snapshot
Sesquiterpenes from Artemisia argyi: Absolute Configurations and Biological Activities
inferred← citeshttps://doi.org/10.1007/s13659-020-00254-0openalex-snapshot
Artemlavanins A and B from Artemisia lavandulaefolia and Their Cytotoxicity Against Hepatic Stellate Cell Line LX2
inferred← citeshttps://doi.org/10.1007/s13659-020-00255-zopenalex-snapshot
Artemyrianins A–G from Artemisia myriantha and Their Cytotoxicity Against HepG2 Cells
inferred← citeshttps://doi.org/10.1016/j.apsb.2020.12.006openalex-snapshot
New guaiane-type sesquiterpenoid dimers from Artemisia atrovirens and their antihepatoma activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103551openalex-snapshot
Polyhydroxyl guaianolide terpenoids as potential NF-кB inhibitors induced cytotoxicity in human gastric adenocarcinoma cell line
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104451openalex-snapshot
Sesquiterpene lactone dimers from Artemisia lavandulifolia inhibit interleukin-1β production in macrophages through activating autophagy
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.10.077openalex-snapshot
New terpenoids and thiophene derivatives from the aerial parts of Artemisia sieversiana
inferred← citeshttps://doi.org/10.1016/j.bse.2010.01.015openalex-snapshot
1, 10-Secoguaianolides from Artemisia anomala (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.bse.2012.07.027openalex-snapshot
Two new sesquiterpene lactones and other chemical constituents of Artemisia roxbughiana
inferred← citeshttps://doi.org/10.1016/j.cbi.2015.08.015openalex-snapshot
Arglabin: From isolation to antitumor evaluation
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.01.017openalex-snapshot
Design, synthesis, and antiviral activity of novel rutin derivatives containing 1, 4-pentadien-3-one moiety
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.12.005openalex-snapshot
NO inhibitory guaianolide-derived terpenoids from Artemisia argyi
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104900openalex-snapshot
Cytotoxic guaianolides and seco-guaianolides from Artemisia atrovirens
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106527openalex-snapshot
Artemiyrianins A-H, guaiane-type sesquiterpenoids from Artemisia myriantha var. pleiocephala and their antihepatoma activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2011.07.008openalex-snapshot
Terpenoids and phenethyl glucosides from Hyssopus cuspidatus (Labiatae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.03.009openalex-snapshot
Cytotoxic sesquiterpene lactones from Artemisia myriantha
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.127openalex-snapshot
Four new isomeric sesquiterpene lactone dimers from Carpesium faberi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00396openalex-snapshot
Artemyrianolides A–S, Cytotoxic Sesquiterpenoids from Artemisia myriantha
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00894openalex-snapshot
Nitric Oxide Inhibitory Dimeric Sesquiterpenoids from Artemisia rupestris
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00867openalex-snapshot
Highly Oxidized Guaianolide Sesquiterpenoids with Potential Anti-inflammatory Activity from Chrysanthemum indicum
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01491openalex-snapshot
Artatrovirenols A and B: Two Cagelike Sesquiterpenoids from Artemisia atrovirens
inferred← citeshttps://doi.org/10.1021/jo0710432openalex-snapshot
Synthesis of Seven-Membered Carbocyclic Rings via a Microwave-Assisted Tandem Oxyanionic 5-exo dig Cyclization−Claisen Rearrangement Process
inferred← citeshttps://doi.org/10.1021/ol2028515openalex-snapshot
An Allenic Pauson–Khand Approach to 6,12-Guaianolides
inferred← citeshttps://doi.org/10.1021/ol501923kopenalex-snapshot
Carpedilactones A–D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi
inferred← citeshttps://doi.org/10.1021/ol900967jopenalex-snapshot
Asymmetric Synthesis of Seven-Membered Carbocyclic Rings via a Sequential Oxyanionic 5-Exo-Dig Cyclization/Claisen Rearrangement Process. Total Synthesis of (−)-Frondosin B
inferred← citeshttps://doi.org/10.1039/b510388fopenalex-snapshot
A facile domino metathetic route to a thapsigargin skeleton
inferred← citeshttps://doi.org/10.1039/c4ra04069dopenalex-snapshot
Nitroalkenes in the synthesis of carbocyclic compounds
inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
Natural disesquiterpenoids: an update
inferred← citeshttps://doi.org/10.1055/a-1554-2866openalex-snapshot
New Guaianolide Sesquiterpene Lactones and Other Constituents from Pyrethrum pulchrum
inferred← citeshttps://doi.org/10.1080/10412905.2009.9700104openalex-snapshot
Essential Oil Profile of Natural-Temperate and Domesticated-SubtropicalArtemisia myrianthaWall. ex Bess. var.pleiocephala(Pamp.) Ling. Plants
inferred← citeshttps://doi.org/10.1080/14786410600823878openalex-snapshot
An unusual sesquiterpenoid fromHypochaeris achyrophorus(Asteraceae)
inferred← citeshttps://doi.org/10.1080/14786419.2013.768991openalex-snapshot
A new guaianolide from Artemisia roxburghiana
inferred← citeshttps://doi.org/10.3998/ark.5550190.0012.505openalex-snapshot
Synthesis of cycloheptanoid natural products via tandem 5-exo cyclization/Claisen rearrangement process
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.7.1841openalex-snapshot
Studies toward Synthesis of Arteminolides: Intramolecular [5+2] Oxidopyrylium Ion Cycloaddition Reactions with Silicon Tether
inferred← citeshttps://doi.org/10.5012/bkcs.2012.33.1.289openalex-snapshot
Synthetic Studies on Arglabin Diene; An Alleged Precursor to Arteminolides
inferred← citeshttps://doi.org/10.5012/bkcs.2014.35.1.23openalex-snapshot
Silicon-Tethered Intramolecular [5+2] Oxidopyrylium-Based Cycloaddition and Reductive Cleavage of Ether Bridge: Synthetic Studies Toward Arteminolides
inferred← citeshttps://doi.org/10.5114/bta.2012.46591openalex-snapshot
REVIEW PAPER Artemisia species in vitro cultures for production of biologically active secondary metabolites
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