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Novel marine sponge alkaloids. 1. Plakinidine A and B, anthelmintic active alkaloids from a Plakortis sponge
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inferred← citeshttps://doi.org/10.11646/zootaxa.3718.6.2zenodo-depositor-declared
Four new species of Plakinidae (Porifera: Homoscleromorpha) from Brazil
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod019openalex-snapshot
Porifera (Sponges)–1
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/ange.19931050104openalex-snapshot
Marine Metaboliten und die Komplexierung von Metall‐Ionen: Tatsachen und Hypothesen
inferred← citeshttps://doi.org/10.1002/anie.199300013openalex-snapshot
Marine Metabolites and Metal Ion Chelation: The Facts and the Fantasies
inferred← citeshttps://doi.org/10.1002/cbdv.200490048openalex-snapshot
Natural‐Product Diversity of the New Caledonian Marine Ecosystem Compared to Other Ecosystems: A Pharmacologically Oriented View
inferred← citeshttps://doi.org/10.1002/chin.199013307openalex-snapshot
ChemInform Abstract: Novel Marine Sponge Alkaloids. Part 1. Plakinidine A (Ia) and B (Ib), Anthelmintic Active Alkaloids from a Plakortis Sponge.
inferred← citeshttps://doi.org/10.1002/ejoc.201300227openalex-snapshot
Bisannulation of 2,3‐Dichloro‐1,4‐naphthoquinone with o‐Nitrophenylacetic Acid Derivatives: A Succinct Synthesis of the ABCD Ring System of Alpkinidine
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A Green Approach for the One‐Pot, Three‐Component Synthesis of 2‐Arylpyrroloacridin‐1(2H)‐Ones using Lactic Acid as a Bio‐based Catalyst under Solvent‐Free Conditions
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Improved and Efficient Synthesis of Pyrrolo[2,3,4‐kl]acridin‐1‐one Derivatives under Ultrasound Irradiation
inferred← citeshttps://doi.org/10.1002/jhet.2023openalex-snapshot
An Efficient Synthesis of Pyrroline‐Fused Acridine Derivatives Catalyzed by Silica Sulfuric Acid
inferred← citeshttps://doi.org/10.1002/jhet.3043openalex-snapshot
Synthesis and Antibacterial Activity of Novel 1H‐indol‐2‐ol Derivatives
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Nematotoxicity of drupacine and a Cephalotaxus alkaloid preparation against the plant‐parasitic nematodes Meloidogyne incognita and Bursaphelenchus xylophilus
inferred← citeshttps://doi.org/10.1002/slct.201601718openalex-snapshot
An Amino Sugar Promoted Green Protocol: A One‐Pot, Meglumine‐Catalyzed, Multicomponent Strategy for Synthesis of Multifaceted Pyrroloacridin‐1(2H)‐one Derivatives
inferred← citeshttps://doi.org/10.1002/slct.201900357openalex-snapshot
A Concise Approach for the Synthesis of the ABCD Ring System of Alpkinidine
inferred← citeshttps://doi.org/10.1002/slct.201904621openalex-snapshot
Microwave‐Assisted Synthesis of Positional Isomeric Dihydro‐triazolo‐pyrimido‐acridines and Biological studies
inferred← citeshttps://doi.org/10.1002/tcr.70239openalex-snapshot
Serendipitous Emergence of Pyrrolo[2,3,4‐ kl ]acridin‐1(2 H )‐one Derivatives: From Unexpected Discovery to Synthetic Development
inferred← citeshttps://doi.org/10.1007/978-1-4615-0747-5_3openalex-snapshot
Class Demospongiae Sollas, 1885
inferred← citeshttps://doi.org/10.1007/978-1-4899-2391-2_7openalex-snapshot
Antitumor and Cytotoxic Compounds from Marine Organisms
inferred← citeshttps://doi.org/10.1007/978-1-4899-2391-2_9openalex-snapshot
The Search for Antiparasitic Agents from Marine Animals
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_12openalex-snapshot
Bioactive Alkaloids from Marine Sponges
inferred← citeshttps://doi.org/10.1007/978-81-322-2794-6_9openalex-snapshot
Biologically Active Metabolites from Sponges and Their Activities
inferred← citeshttps://doi.org/10.1007/s10600-015-1508-0openalex-snapshot
New Indole Alkaloids from the Sponge Plakortis sp.
inferred← citeshttps://doi.org/10.1007/s11144-019-01709-3openalex-snapshot
Chemoselective synthesis of drug-like pyrrolo[2,3,4-kl]acridin-1-one using polyoxometalate@lanthanoid catalyst
inferred← citeshttps://doi.org/10.1007/s40995-016-0133-5openalex-snapshot
Eco-Friendly and Facile Approach Toward a One-Pot Synthesis of 2-Arylpyrrolo[2,3,4-kl]acridin-1(2H)-ones Catalyzed by Acetic Acid Under Solvent-Free Conditions
inferred← citeshttps://doi.org/10.1016/0040-4039(91)85064-copenalex-snapshot
Neamphine, a sulfur containing aromatic heterocycle isolated from the marine sponge neamphius huxleyi
inferred← citeshttps://doi.org/10.1016/b978-0-323-95931-5.00008-7openalex-snapshot
Multicomponent reactions and its application with ionic liquid
inferred← citeshttps://doi.org/10.1016/b978-0-444-63462-7.00009-9openalex-snapshot
Alkaloids: A Source of Anticancer Agents from Nature
inferred← citeshttps://doi.org/10.1016/b978-0-7506-9003-4.50020-4openalex-snapshot
Modern Spectroscopic Approaches to Structure Elucidation
inferred← citeshttps://doi.org/10.1016/bs.aihch.2020.01.001openalex-snapshot
The Friedländer reaction: A powerful strategy for the synthesis of heterocycles
inferred← citeshttps://doi.org/10.1016/bs.alkal.2023.06.001openalex-snapshot
Marine pyridoacridine, pyridoacridone and pyrroloacridine alkaloids
inferred← citeshttps://doi.org/10.1016/j.bmcl.2008.05.078openalex-snapshot
Novel fluorinated acridone derivatives. Part 1: Synthesis and evaluation as potential anticancer agents
inferred← citeshttps://doi.org/10.1016/j.saa.2012.04.015openalex-snapshot
Synthesis, spectral characterization and larvicidal activity of acridin-1(2H)-one analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2004.03.057openalex-snapshot
Synthetic studies of benzo[b]pyrrolo[4,3,2-de][1,10]phenanthroline
inferred← citeshttps://doi.org/10.1016/j.tet.2009.10.109openalex-snapshot
Ecionines A and B, two new cytotoxic pyridoacridine alkaloids from the Australian marine sponge, Ecionemia geodides
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135043openalex-snapshot
Metal-free one-pot synthesis of pyrroloacridine derivatives mediated by achiral nicotinic acid
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.044openalex-snapshot
A short route to the synthesis of pyrroloacridines via Ullmann–Goldberg condensation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.048openalex-snapshot
A facile regio- and stereoselective synthesis of novel dispirooxindolyl-[acridine-2′,3-pyrrolidine/thiapyrrolizidine]-1′-ones via 1,3-dipolar cycloaddition of azomethine ylides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.070openalex-snapshot
An unexpected multicomponent reaction leading to 2-arylpyrrolo[2,3,4-kl]acridin-1(2H)-ones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.105openalex-snapshot
A facile sequential three-component regio- and stereoselective synthesis of novel spiro-isoxazoline/acridinone hybrids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.059openalex-snapshot
Acid-mediated cyclizations of SEM-protected heterocyclic anilines and adjacent hydroxyls or enol-ethers
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155518openalex-snapshot
Greener synthesis of Pyrroloacridine-1(2H)-one and 1,8-Dioxodecahydroacridine derivatives: Ascorbic acid mediated OrganocatalyticApproach
inferred← citeshttps://doi.org/10.1016/j.ultsonch.2014.06.015openalex-snapshot
Simultaneous sonication assistance for the synthesis of pyrroloacridinones and its efficient catalyst HBF4 supported on uniform spherical silica nanoparticles
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)80872-3openalex-snapshot
Using spectroscopic and database strategies to unravel structures of polycyclic bioactive marine sponge sesterterpenes
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00332-4openalex-snapshot
Metabolites from the sponge Plakortis simplex. Determination of absolute stereochemistry of plakortin. Isolation and stereostructure of three plakortin related compounds
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)85977-8openalex-snapshot
Novel marine sponge alkaloids 3. β-carbolinium salts from Fascaplysinopsis reticulata
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)92247-0openalex-snapshot
Plakotenin, a new cytotoxic carboxylic acid from the okinawan marine sponge plakortis Sp.
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00671-3openalex-snapshot
Structures and cytotoxicities of fascaplysin and related alkaloids from two marine phyla—Fascaplysinopsis sponges and Didemnum tunicates
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60930-7openalex-snapshot
Heterocycle-Fused Acridines
inferred← citeshttps://doi.org/10.1016/s0065-7743(08)61204-xopenalex-snapshot
Chapter 17. Antiparasitic Agents
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60105-4openalex-snapshot
Chapter 2 Marine Alkaloids II
inferred← citeshttps://doi.org/10.1016/s1521-4478(06)80007-7openalex-snapshot
Recent developments in the synthesis of marine pyridoacridine alkaloids
inferred← citeshttps://doi.org/10.1016/s1572-5995(02)80013-8openalex-snapshot
Secondary metabolites with antinematodal activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00302openalex-snapshot
Evaluating Nitrogen-Containing Biosynthetic Products Produced by Saltwater Culturing of Several California Littoral Zone Gram-Negative Bacteria
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01386openalex-snapshot
Synthesis of Stable N–H Imines with a Benzo[7,8]indolizine Core and Benzo[7,8]indolizino[1,2-c]quinolines via Copper-Catalyzed Annulation of α,β-Unsaturated O-Acyl Ketoximes with Isoquinolinium N-Ylides
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03922openalex-snapshot
Photochemical Dimerization of Plakinidine B Leads to Potent Inhibition of the E3 Ubiquitin-Protein Ligase CBL-B
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03868openalex-snapshot
Mn(III)-Mediated Cascade Cyclization of 3-Isocyano-[1,1′-biphenyl]-2-carbonitrile with Arylboronic Acid: Construction of Pyrrolopyridine Derivatives
inferred← citeshttps://doi.org/10.1021/acschemneuro.6b00167openalex-snapshot
Identification of the First Marine-Derived Opioid Receptor “Balanced” Agonist with a Signaling Profile That Resembles the Endorphins
inferred← citeshttps://doi.org/10.1021/acsomega.2c02116openalex-snapshot
Toward the Total Synthesis of Alpkinidine: Synthesis of Haloquinone CE Ring System Synthons and Attempted Nucleophilic Bisannulation
inferred← citeshttps://doi.org/10.1021/ar00031a003openalex-snapshot
Selective electrophilic activation of alkanes
inferred← citeshttps://doi.org/10.1021/ci200619yopenalex-snapshot
INFERCNMR: A 13C NMR Interpretive Library Search System
inferred← citeshttps://doi.org/10.1021/cr040630+openalex-snapshot
Total Synthesis of Selected Bioactive Natural Products: Illustration of Strategy and Design
inferred← citeshttps://doi.org/10.1021/ic971435zopenalex-snapshot
Structural Studies of a Borane-Modified Phosphate Diester Linkage: Ab Initio Calculations on the Dimethylboranophosphate Anion and the Single-Crystal X-ray Structure of Its Diisopropylammonium Salt
inferred← citeshttps://doi.org/10.1021/ja952277iopenalex-snapshot
Synthesis and Physical Properties of Highly Sulfonated Polyaniline
inferred← citeshttps://doi.org/10.1021/ja962334nopenalex-snapshot
Double Stereochemical Labeling in Stilbene Photochemistry: Tracing Phenyl Rotation Reveals Stereochemically Distinct Reaction Pathways for Formation of the E Photoproducts
inferred← citeshttps://doi.org/10.1021/jo026459oopenalex-snapshot
Structures and Cytotoxic Properties of Sponge-Derived Bisannulated Acridines
inferred← citeshttps://doi.org/10.1021/jo0489871openalex-snapshot
Simple, Facile, and One-Pot Conversion of the Baylis−Hillman Adducts into Functionalized 1,2,3,4-Tetrahydroacridines and Cyclopenta[b]quinolines
inferred← citeshttps://doi.org/10.1021/jo050420copenalex-snapshot
A Convenient Route to Diverse Heterocycles through an Addition of β-Amino Carbonyl Compounds to 3-Halogeno-4-methoxybenzynes
inferred← citeshttps://doi.org/10.1021/jo400539xopenalex-snapshot
Tandem Synthesis of Pyrroloacridones via [3 + 2] Alkyne Annulation/Ring-Opening with Concomitant Intramolecular Aldol Condensation
inferred← citeshttps://doi.org/10.1021/jo981377eopenalex-snapshot
Amphilactams A−D: Novel Nematocides from Southern Australian Marine Sponges of the Genus Amphimedon
inferred← citeshttps://doi.org/10.1021/jp0630471openalex-snapshot
Photoinduced Electron-Transfer Reactions in Two Room-Temperature Ionic Liquids: 1-Butyl-3-methylimidazolium Hexafluorophosphate and 1-Octyl-3-methylimidazolium Hexafluorophosphate
inferred← citeshttps://doi.org/10.1021/jp980383bopenalex-snapshot
Photophysical and Photochemical Investigation of a Dodecafluorosubphthalocyanine Derivative
inferred← citeshttps://doi.org/10.1021/np060585wopenalex-snapshot
Pyrroloacridine Alkaloids from Plakortis quasiamphiaster: Structures and Bioactivity
inferred← citeshttps://doi.org/10.1021/np800184gopenalex-snapshot
Marine Natural Product Libraries for High-Throughput Screening and Rapid Drug Discovery
inferred← citeshttps://doi.org/10.1021/np800817yopenalex-snapshot
A Selective Account of Effective Paradigms and Significant Outcomes in the Discovery of Inspirational Marine Natural Products
inferred← citeshttps://doi.org/10.1021/np970312oopenalex-snapshot
Plakinidine D, a New Pyrroloacridine Alkaloid from the Ascidian Didemnum rubeum
inferred← citeshttps://doi.org/10.1021/ol302058gopenalex-snapshot
An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l -Proline
inferred← citeshttps://doi.org/10.1021/ol400322vopenalex-snapshot
Highly Selective Domino Multicyclizations for Forming Polycyclic Fused Acridines and Azaheterocyclic Skeletons
inferred← citeshttps://doi.org/10.1021/ol400371hopenalex-snapshot
Sc(OTf)3-Catalyzed Dehydrogenative Cyclization for Synthesis of N-Methylacridones
inferred← citeshttps://doi.org/10.1021/ol402164sopenalex-snapshot
A Concise Construction of Polycyclic Quinolines via Annulation of ω-Cyano-1-alkynes with Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1021/ol901916popenalex-snapshot
Unprecedented Bridged Annulation Approach to the Construction of 5,6-Dihydro-4H-benzo[kl]acridines
inferred← citeshttps://doi.org/10.1039/c2np20055dopenalex-snapshot
Investigations of the marine flora and fauna of the Fiji Islands
inferred← citeshttps://doi.org/10.1039/c2ob26315gopenalex-snapshot
A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives
inferred← citeshttps://doi.org/10.1039/c4ra01287aopenalex-snapshot
Covalently anchored carboxylic acid on uniform spherical silica nanoparticles with narrow slit like mesopores for the synthesis of pyrroloacridinones: CuI-catalyzed further C(sp3)–H oxyfunctionalization for CO formation
inferred← citeshttps://doi.org/10.1039/c5ra11747jopenalex-snapshot
Amidic C–N bond cleavage of isatin: chemoselective synthesis of pyrrolo[2,3,4- kl ]acridin-1-ones using Ag NPs decorated rGO composite as an efficient and recoverable catalyst under microwave irradiation
inferred← citeshttps://doi.org/10.1039/c6ra18048eopenalex-snapshot
Single step incorporation of isatin to enaminone: a recyclable catalyst towards assembly of diverse four ring fused pyrrolo[2,3,4-kl]acridin-1-ones
inferred← citeshttps://doi.org/10.1039/d2nj04082dopenalex-snapshot
One-pot Mannich/aza-Wittig/deaminative aromatization reactions for the synthesis of 1,2,3,4-tetrahydroacridines and cyclohepta[ b ]quinolines
inferred← citeshttps://doi.org/10.1039/d2ob00547fopenalex-snapshot
Synthesis of triarylphosphines from arylammonium salts via one-pot transition-metal-free C–P coupling
inferred← citeshttps://doi.org/10.1039/d3np00019bopenalex-snapshot
Natural products as anthelmintics: safeguarding animal health
inferred← citeshttps://doi.org/10.1039/d4qo00169aopenalex-snapshot
Concise synthesis of pyrrolo[3,4- c ]quinolines via a P(NMe 2 ) 3 -catalyzed [4 + 2] annulation followed by a Zn/AcOH-mediated reduction–hydroamination–isomerization
inferred← citeshttps://doi.org/10.1080/00397911.2016.1204462openalex-snapshot
Synthesis of 2H-pyrrolo[3,4-C]quinoline via an Aldol/Van Leusen/Staudinger/aza-Wittig sequence
inferred← citeshttps://doi.org/10.1080/00397911.2017.1421665openalex-snapshot
β-Cyclodextrin catalyzed one-pot four component auspicious protocol for synthesis of spiro[acridine-9,3′-indole]-2′,4,4′(1′H,5′H,10H)-trione as a potential antimicrobial agent
inferred← citeshttps://doi.org/10.1080/10406638.2018.1481115openalex-snapshot
A One-pot Multicomponent Synthesis of Pyrroloacridine-1(2H)-one and 1,8-Dioxodecahydroacridine Derivatives Catalyzed by Salicylic Acid in Polyethylene Glycol
inferred← citeshttps://doi.org/10.1080/14786410701526024openalex-snapshot
Benhamycin, novel alkaloid from terrestrialStreptomycessp.
inferred← citeshttps://doi.org/10.3390/molecules18021613openalex-snapshot
Microwave-Assisted Improved Synthesis of Pyrrolo[2,3,4-kl]acridine and Dihydropyrrolo[2,3,4-kl]acridine Derivatives Catalyzed by Silica Sulfuric Acid
inferred← citeshttps://doi.org/10.3390/molecules25092070openalex-snapshot
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products
inferred← citeshttps://doi.org/10.3390/molecules25245862openalex-snapshot
Grindstone Chemistry: Design, One-Pot Synthesis, and Promising Anticancer Activity of Spiro[acridine-9,2′-indoline]-1,3,8-trione Derivatives against the MCF-7 Cancer Cell Line
inferred← citeshttps://doi.org/10.3390/molecules26154534openalex-snapshot
Natural Products from Tongan Marine Organisms
inferred← citeshttps://doi.org/10.3987/com-13-s(s)65openalex-snapshot
Regioselective Multicomponent Domino Reactions Providing Rapid and Efficient Routes to Fused Acridines
inferred← citeshttps://doi.org/10.3987/com-18-s(f)26openalex-snapshot
Synthetic Studies on Plakinidines
inferred← citeshttps://doi.org/10.3987/rev-04-sr(p)1openalex-snapshot
Metabolites from Marine Sponges of the Genus Plakortis
inferred← citeshttps://doi.org/10.3998/ark.5550190.p008.948openalex-snapshot
New cytotoxic cyclic peroxide acids from Plakortis sp. marine sponge
inferred← citeshttps://doi.org/10.70675/e1f90413z5e0dz40c6zbd12zfb9360e627bbopenalex-snapshot
Recherche de molecules naturelles bioactives issues de la biodiversite marine de la zone sud-ouest de l'ocean Indien
inferred← citeshttps://doi.org/10.7164/antibiotics.50.543openalex-snapshot
Lymphostin (LK6-A), a Novel Immunosuppressant from Streptomyces sp. KY11783: Structural Elucidation.
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