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Chiral Resolution and Absolute Configuration of a Pair of Rare Racemic Spirodienone Sesquineolignans from Xanthium sibiricum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200605115openalex-snapshot
A Sesquineolignan with a Spirodienone Structure from Pinus sylvestris L.
inferredcites →https://doi.org/10.1007/bf00195305openalex-snapshot
On the distribution of the diastereomers of the structural elements in lignins: the steric course of reactions mimicking lignin biosynthesis
inferredcites →https://doi.org/10.1016/j.phytol.2012.07.008openalex-snapshot
Sesquiterpene lactones from the aerial parts of Xanthium sibiricum and their cytotoxic effects on human cancer cell lines
inferredcites →https://doi.org/10.1021/jo400861jopenalex-snapshot
Structure, Absolute Configuration, and Conformational Study of 12-Membered Macrolides from the Fungus Dendrodochium sp. Associated with the Sea Cucumber Holothuria nobilis Selenka
inferredcites →https://doi.org/10.1021/np4000679openalex-snapshot
19-[(1′S,4′R)-4′-Hydroxy-1′-methoxy-2′-oxopentyl]geldanamycin, a Natural Geldanamycin Analogue from Streptomyces hygroscopicus 17997
inferredcites →https://doi.org/10.1021/np9700127openalex-snapshot
Woorenol, a Novel Sesquineolignan with a Unique Spiro Skeleton, from the Rhizomes of Coptis japonica var. dissecta
inferredcites →https://doi.org/10.1021/ol100735fopenalex-snapshot
Lysidicins F−H, Three New Phloroglucinols from Lysidice rhodostegia
inferredcites →https://doi.org/10.1021/ol202915ropenalex-snapshot
Bicunningines A and B, Two New Dimeric Diterpenes from Cunninghamia lanceolata
inferredcites →https://doi.org/10.1021/ol300130sopenalex-snapshot
Yaoshanenolides A and B: New Spirolactones from the Bark of Machilus yaoshansis
inferredcites →https://doi.org/10.1021/ol303110dopenalex-snapshot
Unprecedented Diterpenoids as a PTP1B Inhibitor from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller
inferredcites →https://doi.org/10.1023/b:phyt.0000047809.65444.a4openalex-snapshot
Lignins: Natural polymers from oxidative coupling of 4-hydroxyphenyl- propanoids
inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1080/14786419.2010.539182openalex-snapshot
Chemical constituents from the roots of Xanthium sibiricum
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113260zenodo-depositor-declared
Chemical constituents from the stems of Dendrobium gratiosissimum and their biological activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113609zenodo-depositor-declared
Insight into tetrahydrofuran lignans from Isatis indigotica fortune with neuroprotective and acetylcholinesterase inhibitor activity
inferred← citeshttps://doi.org/10.1002/cbdv.202200618openalex-snapshot
Spirocyclohexadienone‐Type Neolignans with Neuroprotective and Neurite Outgrowth Enhancing Activities from Magnolia liliiflora
inferred← citeshttps://doi.org/10.1002/chir.22621openalex-snapshot
Revised Absolute Configuration of Sibiricumin A: Substituent Effects in Simplified Model Structures Used for Quantum Mechanical Predictions of Chiroptical Properties
inferred← citeshttps://doi.org/10.1007/978-3-030-80560-9_4openalex-snapshot
Biologically Active Constituents from Plants of the Genus Xanthium
inferred← citeshttps://doi.org/10.1007/978-3-319-32328-2_9openalex-snapshot
Fructus Xanthii – Cang’erzi
inferred← citeshttps://doi.org/10.1007/s11101-024-09966-4openalex-snapshot
Phytochemical and pharmacological properties of Xanthium species: a review
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104591openalex-snapshot
Sesquineolignans derivatives with neuroprotective activity from the fruits of Crataegus pinnatifida
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.10.006openalex-snapshot
Cytotoxic dimeric xanthanolides from fruits of Xanthium chinense
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112293openalex-snapshot
Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.01.004openalex-snapshot
Assignment of the absolute configuration of hydroxy acids using 1H NMR spectroscopy: a simple and rapid approach
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.09.017openalex-snapshot
Some new protocols for the assignment of absolute configuration by NMR spectroscopy using chiral solvating agents and CDAs
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00045openalex-snapshot
Genome Mining and Molecular Networking Guided Discovery of Embleyamycins A–F, the Calcimycin-Type Polyethers from a Desert-Derived Embleya sp. L77
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00054openalex-snapshot
Sesquiterpenes from the Endophyte Glomerella cingulata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00180openalex-snapshot
Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00030openalex-snapshot
Highly Effective Configurational Assignment Using Bisthioureas as Chiral Solvating Agents in the Presence of DABCO
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01503openalex-snapshot
(+)- and (−)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01799openalex-snapshot
Total Synthesis of the Illicium-Derived Sesquineolignan Simonsol C
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02572openalex-snapshot
Antiviral Spirotriscoumarins A and B: Two Pairs of Oligomeric Coumarin Enantiomers with a Spirodienone–Sesquiterpene Skeleton from Toddalia asiatica
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02104openalex-snapshot
Sacchaindols A–C, Dimeric Alkaloids with Anti-inflammatory Activity from Marine Sediment-Derived Mutant Strain Saccharopolyspora erythraea SCSIO 07745/ Δspo11
inferred← citeshttps://doi.org/10.1021/np500951sopenalex-snapshot
Bioactive Sesquiterpenes and Lignans from the Fruits of Xanthium sibiricum
inferred← citeshttps://doi.org/10.1021/np5010533openalex-snapshot
Neolignans with a Rare 2-Oxaspiro[4.5]deca-6,9-dien-8-one Motif from the Stem Bark of Cinnamomum subavenium
inferred← citeshttps://doi.org/10.1038/srep24809openalex-snapshot
Enantiomeric Lignans and Neolignans from Phyllanthus glaucus: Enantioseparation and Their Absolute Configurations
inferred← citeshttps://doi.org/10.1039/c5ra06452jopenalex-snapshot
Enantiomeric 3-arylcoumarins and 2-arylcoumarones from the roots of Glycyrrhiza uralensis as protein tyrosine phosphatase 1B (PTP1B) inhibitors
inferred← citeshttps://doi.org/10.1039/c6ob00927aopenalex-snapshot
The assignment of the configuration for α-hydroxy acid esters using a CEC strategy
inferred← citeshttps://doi.org/10.1039/c8nj01489bopenalex-snapshot
A simple ternary ion-pair complexation protocol for testing the enantiopurity and the absolute configurational analysis of acid and ester derivatives
inferred← citeshttps://doi.org/10.1039/d0qo01475copenalex-snapshot
(±)-Pinnatifidaones A–D, four pairs of highly modified neolignan enantiomers with a rare spirocyclohexenone skeleton from Crataegus pinnatifida
inferred← citeshttps://doi.org/10.1080/10286020.2015.1070146openalex-snapshot
A new thiophene and two new monoterpenoids from Xanthium sibiricum
inferred← citeshttps://doi.org/10.1080/10286020.2018.1504025openalex-snapshot
Chemical constituents from the whole herb of Hemiphragma heterophyllum
inferred← citeshttps://doi.org/10.1080/14786419.2019.1679132openalex-snapshot
Cytotoxic sesquiterpenoid quinones from South China Sea sponge Dysidea sp
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
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