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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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inferred← citeshttps://doi.org/10.1002/mrc.1912openalex-snapshot
Long‐range JCH heteronuclear coupling constants in cyclopentane derivatives. Part II
inferred← citeshttps://doi.org/10.1002/mrc.1971openalex-snapshot
A quantitative application of the J‐based configuration analysis method to a flexible small molecule
inferred← citeshttps://doi.org/10.1002/mrc.2182openalex-snapshot
Stereochemistry of cyclopentane derivatives from 2, 3JCH dependence on dihedral angle (θ HCCX)
inferred← citeshttps://doi.org/10.1002/mrc.3965openalex-snapshot
Recent advances in the structure elucidation of small organic molecules by the LSD software
inferred← citeshttps://doi.org/10.1002/mrc.4322openalex-snapshot
Improving the performance of J‐modulated ADEQUATE experiments through homonuclear decoupling and non‐uniform sampling
inferred← citeshttps://doi.org/10.1002/mrc.4396openalex-snapshot
Conformation analysis of d ‐glucaric acid in deuterium oxide by NMR based on its JHH and JCH coupling constants
inferred← citeshttps://doi.org/10.1002/mrc.4400openalex-snapshot
Di(ethylene glycol) methyl ether methacrylate (DEGMEMA)‐derived gels align small organic molecules in methanol
inferred← citeshttps://doi.org/10.1002/mrc.4700openalex-snapshot
Broadband homonuclear decoupled HSQMBC methods
inferred← citeshttps://doi.org/10.1002/mrc.4761openalex-snapshot
Assignment of 1H ‐ and 13C‐NMR data for four helminthosporol analogs with the bicyclo[3.2.1]oct‐6‐ene framework
inferred← citeshttps://doi.org/10.1002/mrc.4983openalex-snapshot
Elucidating heteroatom influence on homonuclear 4J(H,H) coupling constants by DFT/NMR approach
inferred← citeshttps://doi.org/10.1002/mrc.5087openalex-snapshot
A DFT/machine‐learning hybrid method for the prediction of 3 J HCCH couplings
inferred← citeshttps://doi.org/10.1002/mrc.5101openalex-snapshot
Karplus relationships of the 2JHNα and 3JΗΝβ couplings in organic azides
inferred← citeshttps://doi.org/10.1002/mrc.5448openalex-snapshot
Hydrogen bond formation may enhance RDC‐based discrimination of enantiomers
inferred← citeshttps://doi.org/10.1002/mrc.70027openalex-snapshot
Structure Elucidation of a Regioisomer and Another Proton‐Deficient Breitfussin Analogue Using Anisotropic NMR
inferred← citeshttps://doi.org/10.1002/mrc.70064openalex-snapshot
Residual Chemical Shift Anisotropies in the Structure Determination of Small Molecules
inferred← citeshttps://doi.org/10.1002/mrc.70076openalex-snapshot
C i SE: Chirality In Silico Structure Elucidation for Stereochemical Assignment of Natural and Synthetic Organic Compounds
inferred← citeshttps://doi.org/10.1002/mrc.807openalex-snapshot
J‐IMPEACH‐MBC: a new concatenated NMR experiment for F1 scalable, J‐resolved HMBC
inferred← citeshttps://doi.org/10.1002/mrc.902openalex-snapshot
Survey of NMR experiments for the determination of nJ(C,H) heteronuclear coupling constants in small molecules
inferred← citeshttps://doi.org/10.1002/rcm.7151openalex-snapshot
Differentiation of prototropic ions in regioisomeric caffeoyl quinic acids by electrospray ion mobility mass spectrometry
inferred← citeshttps://doi.org/10.1002/slct.202503456openalex-snapshot
Isolation, Structure Elucidation, and Antioxidant Activity of Chemical Constituents from Artocarpus lakoocha Fruits
inferred← citeshttps://doi.org/10.1007/128_2008_9openalex-snapshot
Macrolide-Based Microtubule-Stabilizing Agents – Chemistry and Structure–Activity Relationships
inferred← citeshttps://doi.org/10.1007/7081_2021_57openalex-snapshot
Synthesis of Chlorosulfolipid Natural Products
inferred← citeshttps://doi.org/10.1007/978-1-4939-6634-9_4openalex-snapshot
Structure Elucidation of Antibiotics by NMR Spectroscopy
inferred← citeshttps://doi.org/10.1007/978-3-540-30880-5_3openalex-snapshot
Bivalve Molluscs as Vectors of Marine Biotoxins Involved in Seafood Poisoning
inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_7openalex-snapshot
Contemporary Strategies in Natural Products Structure Elucidation
inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_8openalex-snapshot
Strategies for Structural Assignment of Marine Natural Products Through Advanced NMR-based Techniques
inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_9openalex-snapshot
NMR Methods for Stereochemical Assignments
inferred← citeshttps://doi.org/10.1007/978-981-10-5966-7_14openalex-snapshot
NMR Studies on Natural Product—Stereochemical Determination and Conformational Analysis in Solution and in Membrane
inferred← citeshttps://doi.org/10.1007/978-981-97-1619-7_3openalex-snapshot
A Long Journey Toward Structure Revision and Total Synthesis of Amphidinol 3
inferred← citeshttps://doi.org/10.1007/978-981-97-6830-1_6openalex-snapshot
NMR Studies on Natural Product—Stereochemical Determination and Conformational Analysis in Solution and in Membrane
inferred← citeshttps://doi.org/10.1007/978-981-99-1714-3_9openalex-snapshot
Synthetic Approach Toward Structural Elucidation of Marine Natural Product Symbiodinolide
inferred← citeshttps://doi.org/10.1007/s00723-019-01178-wopenalex-snapshot
NMR Study of Spatial Structure and Internal Dynamic of Adducts of Ninhydrin-Derived Azomethine Ylide with Cyclopropenes
inferred← citeshttps://doi.org/10.1007/s00723-022-01496-6openalex-snapshot
Regioisomers of 2,5,6,7,8-Pentaaryl-1H-Azepino[3,2,1-ij]Quinazoline-1,3(2H)-Dione Containing Various Aryl Substituents in the Azepine Ring: Structure Determination Using NMR Methods
inferred← citeshttps://doi.org/10.1007/s11418-025-01953-zopenalex-snapshot
Two novel resveratrol dimers from Vatica albiramis: structural elucidation and UV-induced formation
inferred← citeshttps://doi.org/10.1007/s11418-026-02045-2openalex-snapshot
Longifoliols A–C, three unprecedented isopimarane derivatives from Callicarpa longifolia
inferred← citeshttps://doi.org/10.1007/s12272-020-01277-4openalex-snapshot
Structure elucidation of small organic molecules by contemporary computational chemistry methods
inferred← citeshttps://doi.org/10.1007/s13659-025-00579-8openalex-snapshot
Polydosetins & pullularins—bioactive tetramic acids & cyclodepsipeptides from the endophytic and nematophagous fungus Polydomus karssenii
inferred← citeshttps://doi.org/10.1007/s42995-020-00066-8openalex-snapshot
Roussoelins A and B: two phenols with antioxidant capacity from ascidian-derived fungus Roussoella siamensis SYSU-MS4723
inferred← citeshttps://doi.org/10.1016/b978-0-08-099986-9.00007-5openalex-snapshot
Correlations Through the Chemical Bond II: Heteronuclear Shift Correlation
inferred← citeshttps://doi.org/10.1016/b978-0-12-385857-3.00001-3openalex-snapshot
Recent Developments in Heteronuclear Multiple-Bond Correlation Experiments
inferred← citeshttps://doi.org/10.1016/b978-0-12-817054-0.00011-4openalex-snapshot
Protein and Enzyme-Related Topics
inferred← citeshttps://doi.org/10.1016/b978-0-444-53836-9.00022-0openalex-snapshot
Novel Bioactive Peptides from Cyanobacteria
inferred← citeshttps://doi.org/10.1016/b978-0-444-63359-0.00007-0openalex-snapshot
Nuclear Magnetic Resonance Spectroscopy for Structural Characterization of Bioactive Compounds
inferred← citeshttps://doi.org/10.1016/b978-012526451-8/50003-5openalex-snapshot
Discovery of New Macrolides from Marine Organisms
inferred← citeshttps://doi.org/10.1016/bs.accb.2022.10.002openalex-snapshot
Pseudo-glycoconjugates with a C-glycoside linkage
inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.04.029openalex-snapshot
Configurational assignments of conformationally restricted bis-monoterpene hydroquinones: Utility in exploration of endangered plants
inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.09.001openalex-snapshot
Assignment of the absolute configuration of hepatoprotective highly oxygenated triterpenoids using X-ray, ECD, NMR J -based configurational analysis and HSQC overlay experiments
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103638openalex-snapshot
Tsaokopyranols A–M, 2,6-epoxydiarylheptanoids from Amomum tsao-ko and their α-glucosidase inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104097openalex-snapshot
Ten new glycosides, carissaedulosides A–J from the root barks of Carissa edulis and their cytotoxicities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104223openalex-snapshot
Rare new bicyclic cembranoid ethers and a novel trihydroxy prenylated guaiane from the Xisha soft coral Lobophytum sp
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104495openalex-snapshot
Identification of fusarielin M as a novel inhibitor of Mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB)
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105156openalex-snapshot
Absolute configuration of polypropionate derivatives: Decempyrones A–J and their MptpA inhibition and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109899openalex-snapshot
Discovery of undescribed lovastatin derivatives from Aspergillus aculeatus: natural quorum sensing inhibitors against Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110054openalex-snapshot
Structually diverse polyketides from an endolicheic fungus Leotiomycetes sp.: discovery of polyene γ-lactone derivatives and antibacterial aspyridone analogues
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.09.029openalex-snapshot
Daedalols A–C, fungal-derived BACE1 inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2013.06.015openalex-snapshot
Isoswinholide B and swinholide K, potently cytotoxic dimeric macrolides from Theonella swinhoei
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.12.003openalex-snapshot
Amphirionin-2, a novel linear polyketide with potent cytotoxic activity from a marine dinoflagellate Amphidinium species
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.11.063openalex-snapshot
Phytochemical and cytotoxic studies on the roots of Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1016/j.bse.2018.12.015openalex-snapshot
Natural products from the medicinal plant Duguetia staudtii (Annonaceae)
inferred← citeshttps://doi.org/10.1016/j.carres.2010.05.003openalex-snapshot
Synthesis and biological activity of ester and ether analogues of α-galactosylceramide (KRN7000)
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.108950openalex-snapshot
Pyridapeptides F‒I, cyclohexapeptides from marine sponge-derived Streptomyces sp. OUCMDZ-4539
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.112293openalex-snapshot
Novel lipopeptides featuring unusual C–C and C–N linkages between cyclic peptides and fatty acyl chains
inferred← citeshttps://doi.org/10.1016/j.cell.2025.11.036openalex-snapshot
Butyrolactol A enhances caspofungin efficacy via flippase inhibition in drug-resistant fungi
inferred← citeshttps://doi.org/10.1016/j.chembiol.2009.06.012openalex-snapshot
Hoiamide A, a Sodium Channel Activator of Unusual Architecture from a Consortium of Two Papua New Guinea Cyanobacteria
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.04.051openalex-snapshot
Cytotoxic oxasqualenoids from the red alga Laurencia viridis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2015.09.033openalex-snapshot
Ring-truncated deguelin derivatives as potent Hypoxia Inducible Factor-1α (HIF-1α) inhibitors
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2018.07.004openalex-snapshot
Progress in using threonine aldolases for preparative synthesis
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104282openalex-snapshot
Polyketides from Alternaria alternata MT-47, an endophytic fungus isolated from Huperzia serrata
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106566openalex-snapshot
Antidiabetic diarylheptanoids from the leaves of Amomum tsao-ko and their inhibition mechanism against α-glucosidase
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106856openalex-snapshot
HSQC−TOCSY fingerprinting-guided isolation of undescribed glycosides and scalemic pentaketides with neuroprotective activity from a mesophotic zone Ircinia sponge-associated fungus, Acremonium sp. NBUF233
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.01.109openalex-snapshot
(1S,3R,4S,5R)5-O-Caffeoylquinic acid: Isolation, stereo-structure characterization and biological activity
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.139496openalex-snapshot
New C-linked diarylheptanoid dimers as potential α-glucosidase inhibitors evidenced by biological, spectral and theoretical approaches
inferred← citeshttps://doi.org/10.1016/j.jff.2015.03.044openalex-snapshot
Quinic acid derivatives from Salicornia herbacea alleviate HMGB1-mediated endothelial dysfunction
inferred← citeshttps://doi.org/10.1016/j.jmr.2005.05.007openalex-snapshot
Spin-edited 2D HSQC–TOCSY experiments for the measurement of homonuclear and heteronuclear coupling constants: Application to carbohydrates and peptides
inferred← citeshttps://doi.org/10.1016/j.jmr.2006.03.015openalex-snapshot
Accurate measurement of long-range heteronuclear coupling constants from undistorted multiplets of an enhanced CPMG-HSQMBC experiment
inferred← citeshttps://doi.org/10.1016/j.jmr.2007.02.005openalex-snapshot
Analyses, extensions and comparison of three experimental schemes for measuring (nJCH+DCH)-couplings at natural abundance
inferred← citeshttps://doi.org/10.1016/j.molstruc.2012.09.024openalex-snapshot
The relative configurations of azalomycins F5a, F4a and F3a
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146831openalex-snapshot
Discovery of protein disulfide isomerase inhibitory megastigmane sesquiterpenoids from Pieris formosa
inferred← citeshttps://doi.org/10.1016/j.phytochem.2006.11.002openalex-snapshot
Sesquiterpene coumarins from Ferula szowitsiana and in vitro antileishmanial activity of 7-prenyloxycoumarins against promastigotes
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.10.003openalex-snapshot
Bioactive jatrophane diterpenes from Euphorbia guyoniana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.01.018openalex-snapshot
Hymenosetin, a 3-decalinoyltetramic acid antibiotic from cultures of the ash dieback pathogen, Hymenoscyphus pseudoalbidus
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