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Rearranged Phloroglucinol-Monoterpenoid Adducts from Callistemon rigidus

https://doi.org/10.1021/acs.jnatprod.7b00606

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What this work says

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

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Application of gradient-enhanced nuclear Overhauser effect spectroscopy (GOESY) in the structure elucidation of plant secondary metabolites

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inferredcites →https://doi.org/10.1007/s11101-009-9152-6openalex-snapshot

Mallotus species from Vietnamese mountainous areas: phytochemistry and pharmacological activities

inferredcites →https://doi.org/10.1016/j.fitote.2016.08.010openalex-snapshot

Acylphloroglucinols from the leaves of Callistemon viminalis

inferredcites →https://doi.org/10.1016/j.foodres.2015.02.023openalex-snapshot

Aboriginal bush foods: A major phloroglucinol from Crimson Bottlebrush flowers (Callistemon citrinus, Myrtaceae) displays strong antinociceptive and anti-inflammatory activity

inferredcites →https://doi.org/10.1016/j.phytochem.2016.08.014openalex-snapshot

Callistiviminenes A-O: Diverse adducts of β-triketone and sesqui- or monoterpene from the fruits of Callistemon viminalis

inferredcites →https://doi.org/10.1016/j.tet.2016.12.076openalex-snapshot

Viminalins A-O: Diverse [3+2] hybrids of acylphloroglucinol and α-phellandrene from the fruits of Callistemon viminalis

inferredcites →https://doi.org/10.1016/j.tet.2017.01.052openalex-snapshot

Acylphloroglucinol derivatives from the twigs and leaves of Callistemon salignus

inferredcites →https://doi.org/10.1016/s0022-2275(20)38283-3openalex-snapshot

Potential bile acid metabolites. 14. Hyocholic and muricholic acid stereoisomers.

inferredcites →https://doi.org/10.1021/acs.joc.5b01658openalex-snapshot

Chlorabietols A–C, Phloroglucinol-Diterpene Adducts from the Chloranthaceae Plant Chloranthus oldhamii

inferredcites →https://doi.org/10.1021/acs.orglett.5b03360openalex-snapshot

Callistrilones A and B, Triketone–Phloroglucinol–Monoterpene Hybrids with a New Skeleton from Callistemon rigidus

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/acs.orglett.6b00685openalex-snapshot

Meroterpenoids with Antiproliferative Activity from a Hawaiian-Plant Associated Fungus Peyronellaea coffeae-arabicae FT238

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Filicinic Acid Based Meroterpenoids with Anti-Epstein–Barr Virus Activities from Hypericum japonicum

inferredcites →https://doi.org/10.1021/acs.orglett.6b01817openalex-snapshot

Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K

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Polycyclic Polyprenylated Acylphloroglucinols

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Structural Biology and Chemistry of the Terpenoid Cyclases

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Enantiospecific, Biosynthetically Inspired Formal Total Synthesis of (+)-Liphagal

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Cytosporolides A−C, Antimicrobial Meroterpenoids with a Unique Peroxylactone Skeleton from Cytospora sp.

inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot

Phloroglucinol compounds of natural origin

inferredcites →https://doi.org/10.1039/b914364popenalex-snapshot

Phloroglucinol compounds of natural origin: Synthetic aspects

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Genome mining and molecular characterization of the biosynthetic gene cluster of a diterpenic meroterpenoid, 15-deoxyoxalicine B, in Penicillium canescens

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Evaluation of the Hepatoprotective Effect of Fumaria parviflora and Momordica balsamina from Saudi Folk Medicine Against Experimentally Induced Liver Injury in Rats

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Correlation between chemical composition and antifungal properties of essential oils of callistemon rigidus and callistemon citrinus of Cameroon against Phaeoramularia angolensis

What points at this work

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

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Undescribed phloroglucinol derivatives with antiviral activities from Dryopteris atrata (Wall. Ex Kunze) Ching

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Antiviral Triketone‐Phloroglucinol‐Monoterpene Adducts from Callistemon rigidus

inferred← citeshttps://doi.org/10.1002/cbdv.201900683openalex-snapshot

Chiral Isolation and Absolute Configuration of (+)‐ and (−)‐Xanchryones F and G from Xanthostemon chrysanthus

inferred← citeshttps://doi.org/10.1002/cbdv.202201111openalex-snapshot

Five New Phenylpropanoyl Phloroglucinol Derivatives from Leptospermum scoparium

inferred← citeshttps://doi.org/10.1007/s00044-021-02703-yopenalex-snapshot

Callistemon genus- a review on phytochemistry and biological activities

inferred← citeshttps://doi.org/10.1007/s00432-019-02905-3openalex-snapshot

Chemopreventive effect of Callistemon citrinus (Curtis) Skeels against colon cancer induced by 1,2-dimethylhydrazine in rats

inferred← citeshttps://doi.org/10.1007/s11101-020-09697-2openalex-snapshot

Phloroglucinols from Myrtaceae: attractive targets for structural characterization, biological properties and synthetic procedures

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Bioactive hybrid compounds from Myrtaceae: Chemical classification and biological activities

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Stelleranoids A–M, guaiane-type sesquiterpenoids based on [5,7] bicyclic system from Stellera chamaejasme and their cytotoxic activity

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Discovery of unusual phloroglucinol–triterpenoid adducts from Leptospermum scoparium and Xanthostemon chrysanthus by building blocks-based molecular networking

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.05.017openalex-snapshot

Four new cinnamoyl-phloroglucinols from the leaves of Xanthostemon chrysanthus

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.08.026openalex-snapshot

Brachyanins A-C, pinene-derived meroterpenoids and phloroglucinol derivative from Leptospermum brachyandrum

inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104968openalex-snapshot

Phloroglucinol-derived lipids from the leaves of Syzygium cumini and their neuroprotective activities

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/10.1016/s1875-5364(18)30131-6openalex-snapshot

Advanced natural products chemistry research in China between 2015 and 2017

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00283openalex-snapshot

Myrcaulones A–C, Unusual Rearranged Triketone–Terpene Adducts from Myrciaria cauliflora

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Camaldulensals A–C, the First Meroterpenoids Possessing Two Spatially Separated Formyl Phloroglucinols Conjugated to a Terpene Core from the Leaves of Eucalyptus camaldulensis Dehnh

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Xanthchrysones A–C: Rearranged Phenylpropanoyl–Phloroglucinol Dimers with Unusual Skeletons from Xanthostemon chrysanthus

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Collective Biomimetic Synthesis of Myrcaulones A and C and Myrcauones B–D

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00238openalex-snapshot

Biomimetic Syntheses of Callistrilones A–E via an Oxidative [3 + 2] Cycloaddition

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Cleistocaltones A and B, Antiviral Phloroglucinol–Terpenoid Adducts from Cleistocalyx operculatus

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Melipatulinones A–C, Three Lignan–Phloroglucinol Hybrids from Melicope patulinervia

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Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana

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Bio-inspired enantioselective total syntheses of (−)-viminalins A, B, H, I, and N and structural reassignment of (−)-viminalin M

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Divergent stereochemical outcomes in the insertion of donor/donor carbenes into the C–H bonds of stereogenic centers

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Advances on the Synthesis of Natural Products with Dihydrobenzofuran Skeleton via Oxidative [3+2] Cycloadditions

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