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Quantum Mechanical–NMR-Aided Configuration and Conformation of Two Unreported Macrocycles Isolated from the Soft Coral Lobophytum sp.: Energy Calculations versus Coupling Constants
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Connecting Discrete Stereoclusters by Using DFT and NMR Spectroscopy: The Case of Nivariol
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Total Synthesis, Stereochemical Revision, and Biological Reassessment of Mandelalide A: Chemical Mimicry of Intrafamily Relationships
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Computational Chemistry to the Rescue: Modern Toolboxes for the Assignment of Complex Molecules by GIAO NMR Calculations
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Beyond DP4: an Improved Probability for the Stereochemical Assignment of Isomeric Compounds using Quantum Chemical Calculations of NMR Shifts
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Rare Cembranoids from Chinese Soft Coral Sarcophyton ehrenbergi: Structural and Stereochemical Studies
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Structure Validation of Complex Natural Products: Time to Change the Paradigm. What did Synthesis of Alstofolinine A Prove?
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DFT/NMR Approach for the Configuration Assignment of Groups of Stereoisomers by the Combination and Comparison of Experimental and Predicted Sets of Data
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Computational Chemistry Driven Solution to Rubriflordilactone B
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Xishacorenes A–C, Diterpenes with Bicyclo[3.3.1]nonane Nucleus from the Xisha Soft Coral Sinularia polydactyla
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Combining the Power of J Coupling and DP4 Analysis on Stereochemical Assignments: The J -DP4 Methods
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Redefining the Impact of Boltzmann Analysis in the Stereochemical Assignment of Polar and Flexible Molecules by NMR Calculations
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Catalyst targets tertiary C–H bonds
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Determination of Relative Configuration in Organic Compounds by NMR Spectroscopy and Computational Methods
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Computational Prediction of 1 H and 13 C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry
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Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability
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Relativistic Force Field: Parametric Computations of Proton–Proton Coupling Constants in 1H NMR Spectra
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Assigning the Stereochemistry of Pairs of Diastereoisomers Using GIAO NMR Shift Calculation
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Stereochemical Determination of Acyclic Structures Based on Carbon−Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products
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Belizentrin, a Highly Bioactive Macrocycle from the Dinoflagellate Prorocentrum belizeanum
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Chemical constituents of the soft corals Sinularia vanderlandi and Sinularia gravis from the coast of Madagascar
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Doubling the power of DP4 for computational structure elucidation
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Recent trends in the structural revision of natural products
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A Brief Review on New Naturally Occurring Cembranoid Diterpene Derivatives from the Soft Corals of the Genera Sarcophyton, Sinularia, and Lobophytum Since 2016
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Squamins C–F, four cyclopeptides from the seeds of Annona globiflora
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Further undescribed cembranoids from South China Sea soft coral Sarcophyton ehrenbergi: Structural elucidation and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113578zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/ange.202113905openalex-snapshot
Hydrocarbon Macrocycle Conformer Ensembles and 13C‐NMR Spectra
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Hydrocarbon Macrocycle Conformer Ensembles and 13 C‐NMR Spectra
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inferred← citeshttps://doi.org/10.1002/cjoc.202000539openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202100236openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202100253openalex-snapshot
Sinucrassins A—K, Casbane‐type Diterpenoids from the South China Sea Soft Coral Sinularia crassa
inferred← citeshttps://doi.org/10.1002/cjoc.202100564openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202100597openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202100676openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13659-021-00303-2openalex-snapshot
Cembranoids of Soft Corals: Recent Updates and Their Biological Activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104223openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105534openalex-snapshot
Diterpenoids from Euphorbia helioscopia and their enhancement of NK cell-mediated killing of NSCLC cells
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114185openalex-snapshot
Gongolarones as antiamoeboid chemical scaffold
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116139openalex-snapshot
Ximaoglaucumins A − F, new cembranoids with anti-inflammatory activities from the South China Sea soft coral Sarcophyton glaucum
inferred← citeshttps://doi.org/10.1016/j.chroma.2024.465416openalex-snapshot
Macrocyclic anti-inflammatory diterpenes from the South China Sea soft coral Sinularia erecta and their isolation by combined column chromatography
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2025.100287openalex-snapshot
Glaucumolides C-P, cembrane-type diterpenoids from the marine soft coral Sarcophyton glaucum with potential attenuating activities against IgAN nephropathy
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104699openalex-snapshot
Bioactive cembrane diterpenoids from the gum resin of Boswellia carterii
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105299openalex-snapshot
Polyoxygenated cembranoids from the South China Sea soft coral Sarcophyton boettgeri and their stereochemistry
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.143077openalex-snapshot
Bioactive C17-norcembranoids and Cembranoids from the Coral Litophyton brassicum of Xisha Island
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113703openalex-snapshot
Cembrane diterpenoids: Chemistry and pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132204openalex-snapshot
Polyoxygenated cembranoids from the Hainan soft coral Lobophytum crassum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153792openalex-snapshot
New diterpenoids from the South China Sea soft coral Sinularia pedunculata
inferred← citeshttps://doi.org/10.1021/acs.jcim.5c02506openalex-snapshot
Solvent Matters: Bridging Theory and Experiment in Quantum-Mechanical NMR Structural Elucidation
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00898openalex-snapshot
Coriaceumins A–D, the First Nitrogen-Containing Crenulide Diterpenoids from the Brown Alga Dictyota coriacea Collected in the East China Sea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00463openalex-snapshot
Unusual Diterpenoids from the South China Sea Soft Coral Sarcophyton ehrenbergi
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02397openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.0c02742openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.1c01218openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03437openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.0c04016openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01601openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsomega.3c06299openalex-snapshot
OSMAC Approach and Cocultivation for the Induction of Secondary Metabolism of the Fungus Pleotrichocladium opacum
inferred← citeshttps://doi.org/10.1038/s41401-022-00980-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41401-024-01347-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1np00030fopenalex-snapshot
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Sarcoeleganolides H–K, new anti-thrombotic cembranes from soft coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.3389/fntpr.2023.1122426openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20090574openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20100602openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20110699openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md21020069openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md21060362openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md21080457openalex-snapshot
Lobosteroids A–F: Six New Highly Oxidized Steroids from the Chinese Soft Coral Lobophytum sp.
inferred← citeshttps://doi.org/10.3390/md21100526openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md22010050openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md22120553openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md23120450openalex-snapshot
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