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Atropisomeric meroterpenoids with rare triketone-phloroglucinol-terpene hybrids from Baeckea frutescens
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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/(sici)1099-1026(1998070)13:4<245::aid-ffj736>3.0.co;2-jopenalex-snapshot
Constituents of the essential oil ofBaeckea frutescens L. from Malaysia
inferredcites →https://doi.org/10.1002/anie.200901719openalex-snapshot
The Challenge of Atropisomerism in Drug Discovery
inferredcites →https://doi.org/10.1002/anie.201606091openalex-snapshot
Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C
inferredcites →https://doi.org/10.1016/0016-7037(95)90151-5openalex-snapshot
Stereochemistry of organic compounds
inferredcites →https://doi.org/10.1016/0031-9422(95)00659-1openalex-snapshot
Phloroglucinols from Baeckea frutescens
inferredcites →https://doi.org/10.1016/0040-4020(96)00510-8openalex-snapshot
Unusual metabolites of Baeckea frutescens
inferredcites →https://doi.org/10.1016/j.bmcl.2017.11.050openalex-snapshot
Recent encounters with atropisomerism in drug discovery
inferredcites →https://doi.org/10.1016/j.fitote.2016.01.013openalex-snapshot
New cytotoxic phloroglucinols, baeckenones D–F, from the leaves of Indonesian Baeckea frutescens
inferredcites →https://doi.org/10.1016/j.phytol.2015.11.011openalex-snapshot
New acylphloroglucinol derivatives from the leaves of Baeckea frutescens
inferredcites →https://doi.org/10.1016/j.tet.2006.06.004openalex-snapshot
Synthesis and separation of the atropisomers of 2-(5-benzo[b]fluorenyl)-2′-hydroxy-1,1′-binaphthyl and related compounds
inferredcites →https://doi.org/10.1016/j.tet.2014.01.031openalex-snapshot
Isolable atropisomers of 2-aryl indoline derivatives: determination of rotational barrier by density functional theory approach
inferredcites →https://doi.org/10.1016/j.tet.2017.01.016openalex-snapshot
New phloroglucinol derivatives from Indonesian Baeckea frutescens
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00042openalex-snapshot
Anti-inflammatory Meroterpenoids from Baeckea frutescens
inferredcites →https://doi.org/10.1021/acs.joc.6b02643openalex-snapshot
Frutescone A–G, Tasmanone-Based Meroterpenoids from the aerial parts of Baeckea frutescens
inferredcites →https://doi.org/10.1021/acs.orglett.6b00650openalex-snapshot
Hyperjapones A–E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum
inferredcites →https://doi.org/10.1021/ja0373162openalex-snapshot
Stereochemistry of Isoplagiochin C, A Macrocyclic Bisbibenzyl from Liverworts
inferredcites →https://doi.org/10.1021/np960419wopenalex-snapshot
Sesquiterpenes from Baeckea frutescens
inferredcites →https://doi.org/10.1071/ch9651405openalex-snapshot
Nuclear magnetic resonance studies. V. The tautomerism of tasmanone and related β-triketones
inferredcites →https://doi.org/10.4155/fmc-2017-0152openalex-snapshot
Atropisomerism in Medicinal Chemistry: Challenges and Opportunities
inferredcites →https://doi.org/10.9734/irjpac/2015/17199openalex-snapshot
Chemical Composition of Essential Oil of Baeckea frutescens L.
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.2022.113308zenodo-depositor-declared
Hyjapones A−D, trimethylated acyphloroglucinol meroterpenoids from Hypericum japonicum thunb. With anti-inflammatory activity
inferred← citeshttps://doi.org/10.1007/s00253-021-11312-zopenalex-snapshot
Peculiarities of meroterpenoids and their bioproduction
inferred← citeshttps://doi.org/10.1007/s11101-020-09697-2openalex-snapshot
Phloroglucinols from Myrtaceae: attractive targets for structural characterization, biological properties and synthetic procedures
inferred← citeshttps://doi.org/10.1007/s11696-021-01865-8openalex-snapshot
Caryophyllene and caryophyllene oxide: a variety of chemical transformations and biological activities
inferred← citeshttps://doi.org/10.1016/b978-0-323-91294-5.00003-8openalex-snapshot
Bioactive hybrid compounds from Myrtaceae: Chemical classification and biological activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.05.008openalex-snapshot
Anti-inflammatory activity of phenolics from Hypericum japonicum
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135101openalex-snapshot
Diels-Alder reaction: A versatile synthetic tool for the synthesis of terpenoids and alkaloids: A review
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155080openalex-snapshot
Biomimetic syntheses of myrtucommulones K-L and N, and callistiviminenes F-H
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00443openalex-snapshot
Camaldulensals A–C, the First Meroterpenoids Possessing Two Spatially Separated Formyl Phloroglucinols Conjugated to a Terpene Core from the Leaves of Eucalyptus camaldulensis Dehnh
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03156openalex-snapshot
Biomimetic Synthesis Enables the Structure Revision of Littordials E and F and Drychampone B
inferred← citeshttps://doi.org/10.1039/c9ob02282aopenalex-snapshot
Rhizophols A and B, antioxidant and axially chiral benzophenones from the endophytic fungus Cytospora rhizophorae
inferred← citeshttps://doi.org/10.1039/c9ob02490eopenalex-snapshot
Biomimetic total syntheses of baefrutones A–D, baeckenon B, and frutescones A, D–F
inferred← citeshttps://doi.org/10.1039/d1np00077bopenalex-snapshot
Recent advances in the synthesis of natural products containing the phloroglucinol motif
inferred← citeshttps://doi.org/10.1039/d1qo00989copenalex-snapshot
A biomimetic synthesis-enabled stereochemical assignment of rhodotomentones A and B, two unusual caryophyllene-derived meroterpenoids from Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1055/a-2706-8264openalex-snapshot
Active Components and Multi-target Mechanism of Tibetan Sinopodophyllum hexandrum Medicine Against Rheumatoid Arthritis Using a CFA-induced Arthritis Rat Model
inferred← citeshttps://doi.org/10.1134/s1070363220070130openalex-snapshot
Axial Chiral Metal Complexes, Carbo- and Heterocycles: Modern Synthesis Strategies and Examples of the Effect of Atropoisomerism on the Structure of Reaction Products
inferred← citeshttps://doi.org/10.1177/1934578x231189143openalex-snapshot
Baeckea frutescens L.: A Review on Phytochemistry, Biosynthesis, Synthesis, and Pharmacology
inferred← citeshttps://doi.org/10.3389/fphar.2022.830103openalex-snapshot
Biological activities of meroterpenoids isolated from different sources
inferred← citeshttps://doi.org/10.3390/biom11070957openalex-snapshot
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology
inferred← citeshttps://doi.org/10.3390/molecules23123370openalex-snapshot
Structures and Bioactive Properties of Myrtucommulones and Related Acylphloroglucinols from Myrtaceae
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