On the public citation graph
New Acyclic 12‐Hydroxygeranylgeraniol‐Derived Diterpenoids from the Seeds of Carpesium triste
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/chin.198242070openalex-snapshot
ChemInform Abstract: GENERAL METHOD FOR DETERMINING ABSOLUTE CONFIGURATION OF ACYCLIC ALLYLIC ALCOHOLS
inferredcites →https://doi.org/10.1007/bf02976551openalex-snapshot
A new cytotoxic acyclic diterpene fromCarpesium divaricatum
inferredcites →https://doi.org/10.1016/j.phytochem.2004.03.014openalex-snapshot
Trihydroxylated linear diterpenes from the brown alga Bifurcaria bifurcata
inferredcites →https://doi.org/10.1016/s0021-9673(01)95493-7openalex-snapshot
Separation of geranylgeraniol isomers by high-performance liquid chromatography and identification by 13C nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1016/s0031-9422(01)00042-5openalex-snapshot
(S)-12-Hydroxygeranylgeraniol-derived diterpenes from the brown alga Bifurcaria bifurcata
inferredcites →https://doi.org/10.1021/ja00377a063openalex-snapshot
General method for determining absolute configuration of acyclic allylic alcohols
inferredcites →https://doi.org/10.1021/np0700570openalex-snapshot
Cytotoxic Germacranolides and Acyclic Diterpenoides from the Seeds of Carpesium triste
inferredcites →https://doi.org/10.1021/np960563hopenalex-snapshot
Napalolides A−D, Four New Sesquiterpene Lactones from Carpesium nepalense
inferredcites →https://doi.org/10.1021/np970157dopenalex-snapshot
Four New Cytotoxic Germacranolides from Carpesium divaricatum
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1246/cl.1985.249openalex-snapshot
ABSOLUTE CONFIGURATION OF CRINITOL. AN ACYCLIC DITERPENE INSECT GROWTH INHIBITOR FROM THE BROWN ALGAE SARGASSUM TORTILE
inferredcites →https://doi.org/10.1248/cpb.49.396openalex-snapshot
Prolyl Endopeptidase Inhibitors from the Underground Part of Rhodiola sachalinensis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4674500openalex-extracted
Carpesabrolide a, a Succinic Acid-Guaiane Merosesquiterpenoid with Anti-Inflammatory Activity from Carpesium Abrotanoides
inferred← citeshttps://doi.org/10.1002/cbdv.202200898openalex-snapshot
Lipskynoids A–G, New Acyclic Diterpenes from the Flowers ofCarpesium lipskyi
inferred← citeshttps://doi.org/10.1002/hlca.201300151openalex-snapshot
Eudesmanolides and Guaianolides from Carpesium triste
inferred← citeshttps://doi.org/10.1007/s10600-015-1383-8openalex-snapshot
A New Sesquiterpenoid from the Flower Buds of Carpesium triste
inferred← citeshttps://doi.org/10.1016/j.jep.2015.01.027openalex-snapshot
The genus Carpesium: A review of its ethnopharmacology, phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.07.010openalex-snapshot
Three new sesquiterpene lactones from Carpesium abrotanoides
inferred← citeshttps://doi.org/10.1021/jo102516aopenalex-snapshot
General and Highly α-Regioselective Zinc-Mediated Prenylation of Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1039/d4ra00292jopenalex-snapshot
Carpesabrolide A, a novel meroterpenoid with anti-inflammatory activity from Carpesium abrotanoides
inferred← citeshttps://doi.org/10.1515/hc-2022-0012openalex-snapshot
Chemical constituents of plants from the genus Carpesium
inferred← citeshttps://doi.org/10.70675/5e45bb7az93d3z4c80zbc60zed1b729bd936openalex-snapshot
Biosynthèse et rôle biologique des diterpènes dans les graines de caféiers
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