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Isolation and Biomimetic Synthesis of (±)-Guajadial B, a Novel Meroterpenoid from Psidium guajava

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cber.18980310308openalex-snapshot
Condensation von Malonsäure mit aromatischen Aldehyden durch Ammoniak und Amine
inferredcites →https://doi.org/10.1002/ejoc.200700682openalex-snapshot
Asymmetric Cyclization of 2′‐Hydroxychalcones to Flavanones: Catalysis by Chiral Brønsted Acids and Bases
inferredcites →https://doi.org/10.1016/j.cclet.2012.05.018openalex-snapshot
Two new triterpenoids from Psidium guajava
inferredcites →https://doi.org/10.1016/j.jep.2008.01.025openalex-snapshot
Psidium guajava: A review of its traditional uses, phytochemistry and pharmacology
inferredcites →https://doi.org/10.1016/s0378-8741(99)00022-7openalex-snapshot
Anticough and antimicrobial activities of Psidium guajava Linn. leaf extract
inferredcites →https://doi.org/10.1021/ol100138kopenalex-snapshot
A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A
inferredcites →https://doi.org/10.1021/ol102179uopenalex-snapshot
Psiguadials A and B, Two Novel Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava
inferredcites →https://doi.org/10.1021/ol702537qopenalex-snapshot
Guajadial: An Unusual Meroterpenoid from Guava Leaves Psidium guajava
inferredcites →https://doi.org/10.1021/ol8005826openalex-snapshot
Camphor Sulfonyl Hydrazines (CaSH) as Organocatalysts in Enantioselective Diels−Alder Reactions
inferredcites →https://doi.org/10.1021/ol9024869openalex-snapshot
Psidials A−C, Three Unusual Meroterpenoids from the Leaves of Psidium guajava L

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C
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Guapsidial A and Guadials B and C: Three New Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1002/chem.202001111openalex-snapshot
Discovery and Biomimetic Synthesis of a Phloroglucinol‐Terpene Adduct Collection from Baeckea frutescens and Its Biogenetic Origin Insight
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New camphor hybrids: lipophilic enhancement improves antimicrobial efficacy against drug-resistant pathogenic microbes and intestinal worms
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Guajadials C-F, four unusual meroterpenoids from Psidium guajava
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Isoprenylated flavonoids and clerodane diterpenoids from Dodonaea viscosa
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Pterocarpadiols A–D, Rare 6a,11b-Dihydroxypterocarpans from Derris robusta
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Clerodane Diterpenoids with Anti-hyperglycemic Activity from Tinospora crispa
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Six-Membered Ring Systems
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The chemical and pharmacological basis of guava (Psidium guajava L.) as potential therapy for type 2 diabetes and associated diseases
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105027openalex-snapshot
Antioxidative and anti-inflammatory activity of psiguadial B and its halogenated analogues as potential neuroprotective agents
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e08465openalex-snapshot
A review on anti-peptic ulcer activities of medicinal plants used in the formulation of Enterica, Dyspepsia and NPK 500 capsules
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Evidence for the efficacy of anti-inflammatory plants used in Brazilian traditional medicine with ethnopharmacological relevance
inferred← citeshttps://doi.org/10.1016/j.jfutfo.2022.12.005openalex-snapshot
A review of meroterpenoids and of their bioactivity from guava (Psidium guajava L.)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114254openalex-snapshot
Acetylcholinesterase inhibitory phloroglucinols from tropic Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.10.008openalex-snapshot
New sesquiterpenoids from Petasites japonicus and Petasites tricholobus
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.10.010openalex-snapshot
New iridoid glycosides from Viburnum punctatum
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104118openalex-snapshot
Rapid microwave-assisted synthesis of meroterpenoids from Psidium guajava
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Viminalins A-O: Diverse [3+2] hybrids of acylphloroglucinol and α-phellandrene from the fruits of Callistemon viminalis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.02.058openalex-snapshot
Synthetic studies on psiguadial B: Construction of bicyclo[4.3.1]decane skeleton via double cyclization reaction of alkyne dicobalt complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.059openalex-snapshot
Biomimetic total synthesis and structure confirmation of myrtucommulone K
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.014openalex-snapshot
Melaleucadines A and B: Two rare benzylic phloroglucinol-terpene hybrids from Melaleuca leucadendron
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c08089openalex-snapshot
Six Unusual Meroterpenoids from the Leaves of Psidium guajava L. and Their PTP1B Inhibitory Activities
inferred← citeshttps://doi.org/10.1021/acs.jafc.7b01762openalex-snapshot
Meroterpenoids with Antitumor Activities from Guava (Psidium guajava)
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00139openalex-snapshot
NMR Fingerprints of Formyl Phloroglucinol Meroterpenoids and Their Application to the Investigation of Eucalyptus gittinsii subsp. gittinsii
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01720openalex-snapshot
Drychampones A–C: Three Meroterpenoids from Dryopteris championii
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02643openalex-snapshot
Frutescone A–G, Tasmanone-Based Meroterpenoids from the aerial parts of Baeckea frutescens
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/10.1021/acs.orglett.5b03117openalex-snapshot
Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01817openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01944openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03299openalex-snapshot
Biomimetic Synthesis of Psiguajdianone Guided Discovery of the Meroterpenoids from Psidium guajava
inferred← citeshttps://doi.org/10.1021/ol502441nopenalex-snapshot
Sterhirsutins A and B, Two New Heterodimeric Sesquiterpenes with a New Skeleton from the Culture of Stereum hirsutum Collected in Tibet Plateau
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Natural product anticipation through synthesis
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Psiguajadials A–K: Unusual Psidium Meroterpenoids as Phosphodiesterase-4 Inhibitors from the Leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1039/c3np70047jopenalex-snapshot
Natural sesquiterpenoids
inferred← citeshttps://doi.org/10.1039/c5ra19651eopenalex-snapshot
Calliviminones C–H: six new hetero- and carbon-Diels–Alder adducts with unusual skeletons from the fruits of Callistemon viminalis
inferred← citeshttps://doi.org/10.1039/c8ob01092gopenalex-snapshot
Biomimetic total syntheses of chromane meroterpenoids, guadials B and C, guapsidial A and psiguajadial D
inferred← citeshttps://doi.org/10.1039/c8ob01388hopenalex-snapshot
Natural products as modulators of the cyclic-AMP pathway: evaluation and synthesis of lead compounds
inferred← citeshttps://doi.org/10.1039/c8ob02687dopenalex-snapshot
Meroterpene-like compounds derived from β-caryophyllene as potent α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1039/c9ob01426hopenalex-snapshot
Bio-inspired enantioselective total syntheses of (−)-viminalins A, B, H, I, and N and structural reassignment of (−)-viminalin M
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/d1ob00693bopenalex-snapshot
Psidguajones A and B, a pair of complex meroterpenoid epimers from the leaves of Psidium guajava
inferred← citeshttps://doi.org/10.1070/rcr4679openalex-snapshot
ortho-Quinone methides as key intermediates in cascade heterocyclizations
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Preparation of isoquercitrin by biotransformation of rutin using α-L-rhamnosidase from Aspergillus niger JMU-TS528 and HSCCC purification
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Novel skeleton sesquiterpenoids isolated from guava leaves
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Four meroterpenoids from the leaves of Psidium guajava L. and their cytotoxicity activities
inferred← citeshttps://doi.org/10.2174/1386207326666230426093315openalex-snapshot
Psidium guajava: An Insight into Ethnomedicinal Uses, Phytochemistry, 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/md11041050openalex-snapshot
(±)-Pestalachloride D, an Antibacterial Racemate of Chlorinated Benzophenone Derivative from a Soft Coral-Derived Fungus Pestalotiopsis sp.
inferred← citeshttps://doi.org/10.3390/molecules181215648openalex-snapshot
Preparative Isolation and Purification of Five Flavonoid Glycosides and One Benzophenone Galloyl Glycoside from Psidium guajava by High-Speed Counter-Current Chromatography (HSCCC)
inferred← citeshttps://doi.org/10.3390/molecules24244536openalex-snapshot
Antileishmanial Compounds Isolated from Psidium Guajava L. Using a Metabolomic Approach
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Psidium guajava L. An Incalculable but Underexplored Food Crop: Its Phytochemistry, Ethnopharmacology, and Industrial Applications
inferred← citeshttps://doi.org/10.70675/a6217c4fzb9abz4348z8391zce379cc8eac8openalex-snapshot
Targeting potentially active compounds from Psidium guajava L. collected from Lao PDR against the Neglected Tropical Diseases using a metabolomic approach
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