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Structural Reassignment of a Marine Metabolite from a Binaphthalenetetrol to a Tetrabrominated Diphenyl Ether
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Asymmetric Total Synthesis of Nigerone and ent‐Nigerone: Enantioselective Oxidative Biaryl Coupling of Highly Hindered Naphthols
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Dynamic Stereochemistry Transfer in a Transannular Aldol Reaction: Total Synthesis of Hypocrellin A
inferredcites →https://doi.org/10.1016/j.tet.2008.01.110openalex-snapshot
Dual activation in oxidative coupling of 2-naphthols catalyzed by chiral dinuclear vanadium complexes
inferredcites →https://doi.org/10.1016/j.tetlet.2004.01.007openalex-snapshot
Dual activation in a homolytic coupling reaction promoted by an enantioselective dinuclear vanadium(IV) catalyst
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Polybrominated oxydiphenol derivatives from the sponge dysidea herbacea
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Highly Enantioselective Oxidative Couplings of 2-Naphthols Catalyzed by Chiral Bimetallic Oxovanadium Complexes with Either Oxygen or Air as Oxidant
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Design, Synthesis, and Investigation of Protein Kinase C Inhibitors: Total Syntheses of (+)-Calphostin D, (+)-Phleichrome, Cercosporin, and New Photoactive Perylenequinones
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Perylenequinone Natural Products: Enantioselective Synthesis of the Oxidized Pentacyclic Core
inferredcites →https://doi.org/10.1021/jo901384hopenalex-snapshot
Perylenequinone Natural Products: Total Syntheses of the Diastereomers (+)-Phleichrome and (+)-Calphostin D by Assembly of Centrochiral and Axial Chiral Fragments
inferredcites →https://doi.org/10.1021/jo9013854openalex-snapshot
Perylenequinone Natural Products: Evolution of the Total Synthesis of Cercosporin
inferredcites →https://doi.org/10.1021/jo901386dopenalex-snapshot
Perylenequinone Natural Products: Total Synthesis of Hypocrellin A
inferredcites →https://doi.org/10.1021/jo9018914openalex-snapshot
Synthesis of the Cores of Hypocrellin and Shiraiachrome: Diastereoselective 1,8-Diketone Aldol Cyclization
inferredcites →https://doi.org/10.1021/np070337fopenalex-snapshot
Cytotoxic Metabolites from an Indonesian Sponge Lendenfeldia sp.
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Asymmetric Total Synthesis of Nigerone
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Enantioselective Total Synthesis of (S)-Bisoranjidiol, an Axially Chiral Bisanthraquinone
inferredcites →https://doi.org/10.1039/b717068hopenalex-snapshot
Chiral dinuclear vanadium(v) catalysts for oxidative coupling of 2-naphthols
inferredcites →https://doi.org/10.1039/b806016aopenalex-snapshot
Dinuclear chiral vanadium catalysts for oxidative coupling of 2-naphthols via a dual activation mechanism
inferredcites →https://doi.org/10.1039/b821092fopenalex-snapshot
Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling
inferredcites →https://doi.org/10.1046/j.1444-2906.2001.00339.xopenalex-snapshot
Four new bioactive bromophenols from the palauan Sponge Phyllospongia dendyi
inferredcites →https://doi.org/10.1080/03014223.1980.11760680openalex-snapshot
A revision of the supraspecific classification of the orders Dictyoceratida, Dendroceratida, and Verongida (class Demospongiae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Undescribed diphenyl ethers betaethrins A-I from a desert plant endophytic strain of the fungus Phoma betae A.B. Frank (Didymellaceae)
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An Integrated Approach to Structure Verification Using Automated Procedures
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Advances in Exploring Mechanisms of Oxidative Phenolic Coupling Reactions
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Reassignments and Corroborations of Oxo‐Bridged Natural Products Directed by OSE and DU8+ NMR Computation
inferred← citeshttps://doi.org/10.1002/anie.201902777openalex-snapshot
Reassignments and Corroborations of Oxo‐Bridged Natural Products Directed by OSE and DU8+ NMR Computation
inferred← citeshttps://doi.org/10.1002/chem.202001884openalex-snapshot
EBC‐232 and 323: A Structural Conundrum Necessitating Unification of Five In Silico Prediction and Elucidation Methods**
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From Natural Compounds to Bioactive Molecules through NMR and In Silico Methodologies
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Reassignment of Improbable Natural Products Identified through Chemical Principle Screening
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Structural Reassignment of Two Polyenol Natural Products
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Automatic assignment of 1H‐NMR spectra of small molecules
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Facilitating quality control for spectra assignments of small organic molecules: nmrshiftdb2 – a free in‐house NMR database with integrated LIMS for academic service laboratories
inferred← citeshttps://doi.org/10.1007/978-3-662-46402-1_4openalex-snapshot
Structure Elucidation Using Strict Structure Generation
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.07.006openalex-snapshot
Synthesis of axially chiral biaryl compounds by asymmetric catalytic reactions with transition metals
inferred← citeshttps://doi.org/10.1016/j.tet.2014.01.005openalex-snapshot
Synthesis of substituted naphthalenes from α-substituted ketones and 1,2-bis(halomethyl)benzenes including a rearrangement aromatization of benzo[c]oxepine
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00322openalex-snapshot
Peganutonin A: Computationally Informed Synthesis of Its Revised Structure
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00685openalex-snapshot
Structural Revision of Natural Dibenzofurans Based on Their Spectroscopic Characteristics
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02859openalex-snapshot
Penicitone: Structural Reassignment of a Proposed Natural Product Acid Chloride
inferred← citeshttps://doi.org/10.1021/ol302195eopenalex-snapshot
Selective Oxidation of 8,8′-Hydroxylated Binaphthols to Bis-spironaphthalenones or Binaphtho-para- and Binaphtho-ortho-quinones
inferred← citeshttps://doi.org/10.1039/d1sc03865fopenalex-snapshot
Cu( i ) catalysis for selective condensation/bicycloaromatization of two different arylalkynes: direct and general construction of functionalized C–N axial biaryl compounds
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The DP5 probability, quantification and visualisation of structural uncertainty in single molecules
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Pitfalls in the structural elucidation of small molecules. A critical analysis of a decade of structural misassignments of marine natural products
inferred← citeshttps://doi.org/10.1039/d3np00009eopenalex-snapshot
Recent advances in oxidative phenol coupling for the total synthesis of natural products
inferred← citeshttps://doi.org/10.2174/1570193x20666230707140919openalex-snapshot
Diphenyl Ethers: Isolation, Bioactivities and Biosynthesis
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-2blsbopenalex-snapshot
The DP5 Probability, Quantification and Visualisation of Structural Uncertainty in Single Molecules
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-2blsb-v2openalex-snapshot
The DP5 Probability, Quantification and Visualisation of Structural Uncertainty in Single Molecules
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-2blsb-v3openalex-snapshot
The DP5 Probability, Quantification and Visualisation of Structural Uncertainty in Single Molecules
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-2blsb-v4openalex-snapshot
The DP5 Probability, Quantification and Visualisation of Structural Uncertainty in Single Molecules
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Valorisation chimique et biotechnologique de la biodiversité marine de l’Archipel des Comores : recherche de molécules naturelles anti-âge
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