On the public citation graph
Antimalarial (+)-trans-Hexahydrodibenzopyran Derivatives from Machaerium multiflorum
0 signed · 85 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.19820940334openalex-snapshot
Makrocyclen aus D- und L-Prolinresten
inferredcites →https://doi.org/10.1007/bf01963954openalex-snapshot
Cannabiripsol: A novelCannabis constituent
inferredcites →https://doi.org/10.1007/bf01963955openalex-snapshot
(−)-Maalian-5-ol, a new enantiomeric sesquiterpenoid from the liverwortPlagiochila ovalifolia
inferredcites →https://doi.org/10.1016/s0031-9422(00)00074-1openalex-snapshot
An antimalarial stilbene from Artocarpus integer
inferredcites →https://doi.org/10.1021/jm00184a002openalex-snapshot
Stereochemical requirements for cannabinoid activity
inferredcites →https://doi.org/10.1021/jm00184a003openalex-snapshot
Fluoroprostaglandins: synthesis and biological evaluation of the methyl esters of (+)-12-fluoro-, (-)-ent-12-fluoro-, (+)-15-epi-fluoro-, and (-)-ent-15-epi-12-fluoroprostaglandin F2.alpha.
inferredcites →https://doi.org/10.1021/jm950934bopenalex-snapshot
Unsaturated Side Chain β-11-Hydroxyhexahydrocannabinol Analogs
inferredcites →https://doi.org/10.1021/np50008a001openalex-snapshot
Constituents of Cannabis sativa L. XVII. A Review of the Natural Constituents
inferredcites →https://doi.org/10.1055/s-2006-960825openalex-snapshot
Antigiardial Isoflavones fromMachaerium aristulatum
inferredcites →https://doi.org/10.1111/j.1536-7150.1991.tb02488.xopenalex-snapshot
The Healing Forest
inferredcites →https://doi.org/10.1111/j.1749-6632.1971.tb13985.xopenalex-snapshot
STRUCTURAL REQUIREMENTS FOR CANNABINOID ACTIVITY*
inferredcites →https://doi.org/10.1248/cpb.15.324openalex-snapshot
Structure and Absolute Configuration of Kessanol and 8-epi-Kessanol
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.2022.113128zenodo-depositor-declared
Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
inferred← citeshttps://doi.org/10.1002/9781118342886.ch9openalex-snapshot
Domino Reactions in the Enantioselective Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/adsc.201100898openalex-snapshot
Enantioselective Synthesis of (−)‐CP‐55940 via Ruthenium‐ Catalyzed Asymmetric Hydrogenation of Ketones
inferred← citeshttps://doi.org/10.1002/adsc.201300294openalex-snapshot
Potassium (E)‐Alkenylaryltrifluoroborates: Orthogonal Functionalization of Haloaryltrifluoroborates via Heck–Mizoroki Reaction
inferred← citeshttps://doi.org/10.1002/ange.201502595openalex-snapshot
Eine kurze und divergente Totalsynthese von (+)‐Machaeriol B, (+)‐Machaeriol D, (+)‐Δ8‐THC und zugehörigen Analoga
inferred← citeshttps://doi.org/10.1002/ange.202302475openalex-snapshot
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids**
inferred← citeshttps://doi.org/10.1002/anie.201502595openalex-snapshot
Short and Divergent Total Synthesis of (+)‐Machaeriol B, (+)‐Machaeriol D, (+)‐Δ8‐THC, and Analogues
inferred← citeshttps://doi.org/10.1002/anie.202302475openalex-snapshot
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids**
inferred← citeshttps://doi.org/10.1002/asia.202500258openalex-snapshot
Intramolecular Diels‐Alder Reaction of Benzo‐Tethered Dienyl Cinnamates: Synthesis of the Tricyclic Core of Morusalisin A
inferred← citeshttps://doi.org/10.1002/cben.202000013openalex-snapshot
Corymbia citriodora: A Valuable Resource from Australian Flora for the Production of Fragrances, Repellents, and Bioactive Compounds
inferred← citeshttps://doi.org/10.1002/chem.201403523openalex-snapshot
Metal‐Free One‐Pot Synthesis of Benzofurans
inferred← citeshttps://doi.org/10.1002/chem.202200405openalex-snapshot
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II
inferred← citeshttps://doi.org/10.1002/dta.3519openalex-snapshot
Hexahydrocannabinol and closely related semi‐synthetic cannabinoids: A comprehensive review
inferred← citeshttps://doi.org/10.1002/ejoc.202001246openalex-snapshot
Evolution of Strategies in Protecting‐Group‐Free Synthesis of Natural Products: A Recent Update
inferred← citeshttps://doi.org/10.1002/hlca.200900014openalex-snapshot
Total Synthesis of (+)‐Machaeriols B and C and of Their Enantiomers with a Cannabinoid Structure
inferred← citeshttps://doi.org/10.1002/slct.202503660openalex-snapshot
Recent Advances in Organometallic Reagents and Catalysts: A Concise Strategy to Synthesize Cannabinoid Natural Products
inferred← citeshttps://doi.org/10.1002/slct.73826openalex-snapshot
Protecting‐Group‐Free Synthesis of CBD‐Like Compounds via Perfluoroboronic Acid‐Mediated Friedel–Crafts Allylation
inferred← citeshttps://doi.org/10.1007/978-3-319-45541-9_2openalex-snapshot
Synthesis of Phytocannabinoids
inferred← citeshttps://doi.org/10.1016/b978-0-12-817903-1.00006-1openalex-snapshot
Progress in studies on meroterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91097-2.00006-6openalex-snapshot
Bioactive stilbenes from plants
inferred← citeshttps://doi.org/10.1016/b978-0-444-63460-3.00002-xopenalex-snapshot
From Bench to Bedside: Natural Products and Analogs for the Treatment of Neglected Tropical Diseases (NTDs)
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104202openalex-snapshot
Metabolites of Machaerium isadelphum as chemophenetic markers of Machaerium genus
inferred← citeshttps://doi.org/10.1016/j.cjac.2025.100589openalex-snapshot
In situ produced palladium nanoparticle-catalyzed efficient synthesis of benzo[c]chromenes and analogues under aerobic and ligand-free conditions in water
inferred← citeshttps://doi.org/10.1016/j.jmgm.2013.12.010openalex-snapshot
Antileishmanial phytochemical phenolics: Molecular docking to potential protein targets
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.08.013openalex-snapshot
Monoterpene-stilbenes and other constituents from Machaerium isadelphum
inferred← citeshttps://doi.org/10.1016/j.tet.2012.04.098openalex-snapshot
Synthesis of heterocycles by domino-Knoevenagel–hetero-Diels–Alder reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134694openalex-snapshot
Cytotoxic activity of secondary metabolites from Machaerium isadelphum and structure-activity relationship of machaeriols and machaeridiols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2003.12.107openalex-snapshot
First synthesis of antimalarial Machaeriols A and B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.11.106openalex-snapshot
Enantioselective synthesis of the tetrahydro-6H-benzo[c]chromenes via Domino Michael–Aldol condensation: control of five stereocenters in a quadruple-cascade organocatalytic multi-component reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.11.076openalex-snapshot
CuI catalyzed domino coupling–cyclization of 2-iodo-phenols and 1-alkynes to the synthesis of 2-substituted benzo[b]furans/furo-pyridines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151579openalex-snapshot
Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes
inferred← citeshttps://doi.org/10.1016/s0079-6468(05)43006-4openalex-snapshot
Recent Advances in the Search for Newer Antimalarial Agents
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00874openalex-snapshot
Plant-Based Modulators of Endocannabinoid Signaling
inferred← citeshttps://doi.org/10.1021/acs.joc.6b03086openalex-snapshot
Divergent Strategy for the Diastereoselective Synthesis of the Tricyclic 6,7-Diaryltetrahydro-6H-benzo[c]chromene Core via Pt(IV)-Catalyzed Cycloaddition of o-Quinone Methides and Olefin Ring-Closing Metathesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01322openalex-snapshot
Asymmetric Synthesis of Functionalized Tricyclic Chromanes via an Organocatalytic Triple Domino Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01005openalex-snapshot
Short and Protecting-Group-Free Approach to the (−)-Δ8-THC-Motif: Synthesis of THC-Analogues, (−)-Machaeriol B and (−)-Machaeriol D
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01857openalex-snapshot
Tetrahydrobenzochromene Synthesis Enabled by a Deconjugative Alkylation/Tsuji–Saegusa–Ito Oxidation on Knoevenagel Adducts
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03752openalex-snapshot
Iron-Catalyzed Enantioselective Intramolecular Inverse Electron-Demand Hetero Diels–Alder Reactions: An Access to Bicyclic Dihydropyran Derivatives
inferred← citeshttps://doi.org/10.1021/acsomega.1c02413openalex-snapshot
Novel Machaeriol Analogues as Modulators of Cannabinoid Receptors: Structure–Activity Relationships of (+)-Hexahydrocannabinoids and Their Isoform Selectivities
inferred← citeshttps://doi.org/10.1021/jacs.4c18319openalex-snapshot
Ligand-Governed Regio- and Enantioselective [2 + 2 + 2] Cycloaddition of 1,7-Enynes: Assembly of the Benzo[c]chromen-1-ol Backbone and Access to Enantioenriched Cannabinol Bioisostere
inferred← citeshttps://doi.org/10.1021/np800328ropenalex-snapshot
Cycloartane Glycosides from Sutherlandia frutescens
inferred← citeshttps://doi.org/10.1021/ol9017326openalex-snapshot
A New Cross-Coupling-Based Synthesis of Carpanone
inferred← citeshttps://doi.org/10.1021/ol902840xopenalex-snapshot
Enantioselective Total Synthesis of (+)-Conicol via Cascade Three-Component Organocatalysis
inferred← citeshttps://doi.org/10.1039/b212695hopenalex-snapshot
Anti-staphylococcal plant natural products
inferred← citeshttps://doi.org/10.1039/c5ra17488kopenalex-snapshot
Recent applications of the hetero Diels–Alder reaction in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/c6np00074fopenalex-snapshot
Phytocannabinoids: a unified critical inventory
inferred← citeshttps://doi.org/10.1039/c7ra03551aopenalex-snapshot
Total synthesis of natural products containing benzofuran rings
inferred← citeshttps://doi.org/10.1039/d2nj02019jopenalex-snapshot
Highly diastereoselective annulation of 2-substituted 3-nitro-2 H -chromenes with hemicurcuminoids and curcuminoids via a double and triple Michael reaction cascade
inferred← citeshttps://doi.org/10.1055/a-1148-9000openalex-snapshot
Natural Phenolic Compounds and Derivatives as Potential Antimalarial Agents
inferred← citeshttps://doi.org/10.1080/14786419.2014.1003062openalex-snapshot
The genusMachaerium(Fabaceae): taxonomy, phytochemistry, traditional uses and biological activities
inferred← citeshttps://doi.org/10.1080/17568919.2025.2580915openalex-snapshot
Recent development of plant-derived and synthetic cannabinoids as novel antimicrobial agents
inferred← citeshttps://doi.org/10.1093/mutage/gev066openalex-snapshot
Chemical and biological characterisation ofMachaerium hirtum(Vell.) Stellfeld: absence of cytotoxicity and mutagenicity and possible chemopreventive potential
inferred← citeshttps://doi.org/10.1111/tmi.70044openalex-snapshot
Cannabis‐Derived Compounds Against Plasmodium sp.: A Systematic Review of Preclinical Studies
inferred← citeshttps://doi.org/10.11606/d.100.2021.tde-28012022-093234openalex-snapshot
Estudo químico e fitotóxico do extrato hidroetanólico das folhas de >i /i< Benth
inferred← citeshttps://doi.org/10.1177/1934578x0800300925openalex-snapshot
Extraction Methods Play a Critical Role in Chemical Profile and Biological Activities of Black Cohosh
inferred← citeshttps://doi.org/10.1186/1756-0500-4-506openalex-snapshot
In vitro antiplasmodial activity of crude extracts of Tetrapleura tetraptera and Copaifera religiosa
inferred← citeshttps://doi.org/10.1201/9781315367583-12openalex-snapshot
The Ecology of Wild Cannabis sativa
inferred← citeshttps://doi.org/10.1201/9781315367583-20openalex-snapshot
Cannabis Chemistry: Cannabinoids in Cannabis, Humans, and Other Species
inferred← citeshttps://doi.org/10.1371/journal.pone.0089566openalex-snapshot
Care and Feeding of the Endocannabinoid System: A Systematic Review of Potential Clinical Interventions that Upregulate the Endocannabinoid System
inferred← citeshttps://doi.org/10.1590/s0100-83582019370100015openalex-snapshot
Phytotoxic Potential of the Crude Extract and Leaf Fractions of Machaerium hirtum on the Initial Growth of Euphorbia heterophylla And Ipomoea grandifolia
inferred← citeshttps://doi.org/10.2174/0118756298307930240531072440openalex-snapshot
A Comprehensive Review on History, Sources, Biosynthesis, Chemical Synthesis and Applications of Stilbenes
inferred← citeshttps://doi.org/10.2174/092986712800229023openalex-snapshot
The Potential of Secondary Metabolites from Plants as Drugs or Leads Against Protozoan Neglected Diseases - Part I
inferred← citeshttps://doi.org/10.2174/09298673113206660291openalex-snapshot
Combating Malaria with Plant Molecules: A Brief Update
inferred← citeshttps://doi.org/10.3390/molecules23010033openalex-snapshot
Recent Advances in Organocatalyzed Domino C–C Bond-Forming Reactions
inferred← citeshttps://doi.org/10.3390/molecules25245885openalex-snapshot
Characterization of α-Glucosidase Inhibitors from Psychotria malayana Jack Leaves Extract Using LC-MS-Based Multivariate Data Analysis and In-Silico Molecular Docking
inferred← citeshttps://doi.org/10.3390/molecules25246000openalex-snapshot
Antimicrobial Constituents from Machaerium Pers.: Inhibitory Activities and Synergism of Machaeriols and Machaeridiols against Methicillin-Resistant Staphylococcus aureus, Vancomycin-Resistant Enterococcus faecium, and Permeabilized Gram-Negative Pathogens
inferred← citeshttps://doi.org/10.3390/molecules27196604openalex-snapshot
Synthesis and Inhibitory Activity of Machaeridiol-Based Novel Anti-MRSA and Anti-VRE Compounds and Their Profiling for Cancer-Related Signaling Pathways
inferred← citeshttps://doi.org/10.3390/molecules28104162openalex-snapshot
Cannabinoid and Opioid Receptor Affinity and Modulation of Cancer-Related Signaling Pathways of Machaeriols and Machaeridiols from Machaerium Pers.
inferred← citeshttps://doi.org/10.3390/molecules28176434openalex-snapshot
Saturated Cannabinoids: Update on Synthesis Strategies and Biological Studies of These Emerging Cannabinoid Analogs
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.