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Racemic Bisindole Alkaloids: Structure, Bioactivity, and Computational Study
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Design and Catalytic Asymmetric Construction of Axially Chiral 3,3′‐Bisindole Skeletons
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Computing chiroptical properties with first‐principles theoretical methods: Background and illustrative examples
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Shermo: A general code for calculating molecular thermochemistry properties
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Exploring stereoselectivity of 3-indolyl cyclopent[b]indoles: A parallel synthesis and anti-EGFR study on human cancer cells
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Synthesis and biological evaluation of curcumin inspired indole analogues as tubulin polymerization inhibitors
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Exhaustive conformational search for transition states: the case of catechol O -methyltransferase active site
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A novel TFA-mediated cyclo-dimerization of 1-substituted 3-alkenylindole derivatives to cyclopent[b]indoles
inferredcites →https://doi.org/10.1016/j.tetlet.2019.151453openalex-snapshot
Lewis acid-catalyzed cyclodimerization of 1-substituted-3-arylvinylindoles leading to highly functionalized fused cyclopenta[b]indoles
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Applications of Deuterium in Medicinal Chemistry
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00452openalex-snapshot
Tulongicin, an Antibacterial Tri-Indole Alkaloid from a Deep-Water Topsentia sp. Sponge
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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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Agelanemoechine, a Dimeric Bromopyrrole Alkaloid with a Pro-Angiogenic Effect from the South China Sea Sponge Agelas nemoechinata
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A series of chiral polybrominated biindoles from the marine blue-green alga Rivularia firma. Application of carbon-13 NMR spin-lattice relaxation data and carbon-13-proton coupling constants to structure elucidation
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Nature of Nonbonded Se···O Interactions Characterized by17O NMR Spectroscopy and NBO and AIM Analyses
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Dearomative Indole (3 + 2) Cycloaddition Reactions
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Discovery of a Potent and Selective Prostaglandin D2 Receptor Antagonist, [(3R)-4-(4-Chloro- benzyl)-7-fluoro-5-(methylsulfonyl)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]-acetic Acid (MK-0524)
inferredcites →https://doi.org/10.1021/jm501100bopenalex-snapshot
Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
inferredcites →https://doi.org/10.1021/jp001062eopenalex-snapshot
Pair Population Analysis within AIM Theory
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Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions
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inferredcites →https://doi.org/10.1021/np060420nopenalex-snapshot
Hyrtinadine A, a Bis-indole Alkaloid from a Marine Sponge
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Antibacterial Anthraquinone Derivatives from a Sea Anemone-Derived Fungus Nigrospora sp.
inferredcites →https://doi.org/10.1021/np4005536openalex-snapshot
Bisindole Alkaloids with Neural Anti-inflammatory Activity from Gelsemium elegans
inferredcites →https://doi.org/10.1021/np500362popenalex-snapshot
Indimicins A–E, Bisindole Alkaloids from the Deep-Sea-Derived Streptomyces sp. SCSIO 03032
inferredcites →https://doi.org/10.1021/ol802506nopenalex-snapshot
Flinderoles A−C: Antimalarial Bis-indole Alkaloids from Flindersia Species
inferredcites →https://doi.org/10.1038/nprot.2008.141openalex-snapshot
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inferredcites →https://doi.org/10.1039/c39850000047openalex-snapshot
Yuehchukene: a novel indole alkaloid with anti-implantation activity
inferredcites →https://doi.org/10.1039/c3ra47056copenalex-snapshot
Highly efficient [3 + 2] reaction of 3-vinylindoles with 3-indolylmethanols by Brønsted-acid catalysis
inferredcites →https://doi.org/10.1039/c5np00032gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferredcites →https://doi.org/10.1039/c5qo00030kopenalex-snapshot
Concise asymmetric total synthesis of bruceolline J
inferredcites →https://doi.org/10.1039/c8ra03480jopenalex-snapshot
Recent metal-catalysed approaches for the synthesis of cyclopenta[ b ]indoles
inferredcites →https://doi.org/10.1055/s-0030-1259688openalex-snapshot
Discovery of an Acid-Promoted [3+2] Cyclodimerization of 3-Vinylindoles and the Development of a General Lewis Acid Catalyzed Process
inferredcites →https://doi.org/10.1063/1.447964openalex-snapshot
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.3389/fphar.2026.1763267openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/antibiotics13121212openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20100649openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules29050933openalex-snapshot
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