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Phosphorus–nitrogen compounds. Part 64. Comparative reactions of spiro and ansa (N/O) cyclotetraphosphazenes with bulky (4-fluorobenzyl) N/N and N/O donor type bidentate reagents: structure, stereogenic properties and cytotoxic activity studies
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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/aoc.6150openalex-snapshot
The comparative reactions of 2‐cis‐4‐ansa and spiro cyclotetraphosphazenes with difunctional ligands: Structural and stereogenic properties, electrochemical, antimicrobial and cytotoxic activity studies
inferredcites →https://doi.org/10.1002/ejic.200901198openalex-snapshot
The Nature of the Phosphazene Nitrogen–Metal Bond: DFT Calculations on 2‐(Pyridyloxy)cyclophosphazene Complexes
inferredcites →https://doi.org/10.1002/ejic.202101067openalex-snapshot
Ferrocenyl Gold Complexes as Efficient Catalysts
inferredcites →https://doi.org/10.1002/jccs.202100475openalex-snapshot
Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies
inferredcites →https://doi.org/10.1002/slct.201700497openalex-snapshot
Antiproliferative Effects against A549, Hep3B and FL Cell Lines of Cyclotriphosphazene‐Based Novel Protic Molten Salts: Spectroscopic, Crystallographic and Thermal Results.
inferredcites →https://doi.org/10.1007/s00394-015-1131-7openalex-snapshot
Antiproliferative activity of the ellagic acid-derived gut microbiota isourolithin A and comparison with its urolithin A isomer: the role of cell metabolism
inferredcites →https://doi.org/10.1007/s10847-009-9578-xopenalex-snapshot
Phosphorus–nitrogen compounds: part 16. Synthesis, stereogenism, anisochronism and the relationship between 31P NMR spectral and crystallographic data of monotopic spiro-crypta phosphazene derivatives
inferredcites →https://doi.org/10.1007/s10870-020-00851-4openalex-snapshot
Synthesis of Bis(2,2,3,3-tetrafluoro-1,4-butanedialkoxy)-2-trans-6-bis(4-fluorobenzyl)spirocyclotetraphosphazene: Structural Characterization, Biological Activity and DFT Studies
inferredcites →https://doi.org/10.1007/s11224-017-1070-4openalex-snapshot
The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene?
inferredcites →https://doi.org/10.1016/0014-2964(79)90137-3openalex-snapshot
Antitumour activity of some cyclophosphazenes
inferredcites →https://doi.org/10.1016/j.apsusc.2007.07.068openalex-snapshot
Modification of Au surfaces using new ferrocene derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2005.09.054openalex-snapshot
Synthesis and in vitro activities of ferrocenic aminohydroxynaphthoquinones against Toxoplasma gondii and Plasmodium falciparum
inferredcites →https://doi.org/10.1016/j.ccr.2006.07.005openalex-snapshot
Cyclophosphazene-based multi-site coordination ligands
inferredcites →https://doi.org/10.1016/j.ccr.2015.01.012openalex-snapshot
Chiral configurations in cyclophosphazene chemistry
inferredcites →https://doi.org/10.1016/j.ejmech.2013.09.046openalex-snapshot
Phosphorus–nitrogen compounds part 27. Syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of new phosphazenes bearing secondary amino and pendant (4-fluorobenzyl)spiro groups
inferredcites →https://doi.org/10.1016/j.ejmech.2014.10.005openalex-snapshot
Phosphorus–nitrogen compounds. Part 29. Syntheses, crystal structures, spectroscopic and stereogenic properties, electrochemical investigations, antituberculosis, antimicrobial and cytotoxic activities and DNA interactions of ansa-spiro-ansa cyclotetraphosphazenes
inferredcites →https://doi.org/10.1016/j.ica.2018.02.025openalex-snapshot
Phosphorus-nitrogen compounds. Part 40. The syntheses of (4-fluorobenzyl) pendant armed cyclotetraphosphazene derivatives: Spectroscopic, crystallographic and stereogenic properties, DNA interactions and antimicrobial activities
inferredcites →https://doi.org/10.1016/j.ica.2018.10.028openalex-snapshot
Phosphorus-nitrogen compounds. Part 44. The syntheses of N,N-spiro bridged cyclotriphosphazene derivatives with (4-fluorobenzyl) pendant arms: Structural and stereogenic properties, DNA interactions, antimicrobial and cytotoxic activities
inferredcites →https://doi.org/10.1016/j.ica.2019.03.018openalex-snapshot
Phosphorus-Nitrogen compounds part 47: The conventional and microwave-assisted syntheses of dispirocyclotriphosphazene derivatives with (4-fluoro/4-nitrobenzyl) pendant arms: Structural and stereogenic properties and DNA interactions
inferredcites →https://doi.org/10.1016/j.ica.2019.119106openalex-snapshot
Phosphorus-nitrogen compounds. Part 52. The reactions of octachlorocyclotetraphosphazene with sodium 3-(N-ferrocenylmethylamino)-1-propanoxide: Investigations of spectroscopic, crystallographic and stereogenic properties
inferredcites →https://doi.org/10.1016/j.ica.2021.120577openalex-snapshot
Amino alcohol based cyclotriphosphazenes: Effects of chain length and base factor on product diversity
inferredcites →https://doi.org/10.1016/j.jfluchem.2006.05.001openalex-snapshot
Chemistry of diphenyltetrafluorophosphazene: Reactions with dilithiated diols
inferredcites →https://doi.org/10.1016/j.jinorgbio.2007.07.003openalex-snapshot
Nanoparticulate platinum(II) anticancer drug: Synthesis and characterization of amphiphilic cyclotriphosphazene–platinum(II) conjugates
inferredcites →https://doi.org/10.1016/j.jorganchem.2012.10.043openalex-snapshot
Synthesis and properties of cyclophosphazenes appended with covalently linked porphyrin–ferrocene conjugates
inferredcites →https://doi.org/10.1016/j.molstruc.2022.132371openalex-snapshot
Novel tetracyclic spermine derivatives of cyclotriphosphazene: Design, synthesis and biological activity
inferredcites →https://doi.org/10.1016/j.poly.2010.07.017openalex-snapshot
Phosphorus–nitrogen compounds: Part 19. Syntheses, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic monoferrocenylcyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2011.05.041openalex-snapshot
Structural properties of new spiro-1,3-propanediaminocyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1016/j.poly.2011.08.035openalex-snapshot
Phosphorus–nitrogen compounds part 22. Syntheses, structural investigations, biological activities and DNA interactions of new mono and bis (4-fluorobenzyl) spirocyclophosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2017.06.054openalex-snapshot
Stereochemical aspects of cyclotriphosphazenes: Prochiral and pseudo-asymmetric phosphorus atoms
inferredcites →https://doi.org/10.1016/j.polymer.2020.122797openalex-snapshot
Using recyclable polystyrene supported cyclic trimeric phosphazene base as catalyst to directly prepare hypotoxic polyesters via ring-opening polymerizations
inferredcites →https://doi.org/10.1016/s0898-8838(02)53005-1openalex-snapshot
Advances in the chemistry of chlorocyclophosphazenes
inferredcites →https://doi.org/10.1016/s1010-6030(00)00213-6openalex-snapshot
Ferrocene and ferrocenyl derivatives in luminescent systems
inferredcites →https://doi.org/10.1021/cr00002a002openalex-snapshot
Regio- and stereochemical control in substitution reactions of cyclophosphazenes
inferredcites →https://doi.org/10.1021/ic0511266openalex-snapshot
Revisiting the Electronic Structure of Phosphazenes
inferredcites →https://doi.org/10.1021/ic062141topenalex-snapshot
Conformational Flexibility in 2,2‘-Dioxybiphenyl-chloro-cyclotetraphosphazenes and its Relevance to Polyphosphazene Analogues
inferredcites →https://doi.org/10.1021/ic101884sopenalex-snapshot
Ring-Closing Metathesis Reactions of Terminal Alkene-Derived Cyclic Phosphazenes
inferredcites →https://doi.org/10.1021/ic3017134openalex-snapshot
Phosphorus–Nitrogen Compounds. Part 24. Syntheses, Crystal Structures, Spectroscopic and Stereogenic Properties, Biological Activities, and DNA Interactions of Novel Spiro-ansa-spiro- and Ansa-spiro-ansa-cyclotetraphosphazenes
inferredcites →https://doi.org/10.1021/ja00839a011openalex-snapshot
General definition of ring puckering coordinates
inferredcites →https://doi.org/10.1021/ja964127topenalex-snapshot
The Dendritic Effect in Molecular Recognition: Ferrocene Dendrimers and Their Use as Supramolecular Redox Sensors for the Recognition of Small Inorganic Anions
inferredcites →https://doi.org/10.1021/jo7025756openalex-snapshot
Negative Hyperconjugation in Phosphorus Stabilized Carbanions
inferredcites →https://doi.org/10.1021/om020760dopenalex-snapshot
Cyclophosphazene Hydrazides as Scaffolds for Multi-Ferrocenyl Assemblies: Synthesis, Structure, and Electrochemistry
inferredcites →https://doi.org/10.1021/sc400283dopenalex-snapshot
Synthesis and Performance of Cyclomatrix Polyphosphazene Derived from Trispiro-Cyclotriphosphazene as a Halogen-Free Nonflammable Material
inferredcites →https://doi.org/10.1039/b104973aopenalex-snapshot
Chiral configurations of spermine-bridged cyclotriphosphazatrienes
inferredcites →https://doi.org/10.1039/b505236jopenalex-snapshot
Achiral molecules in non-centrosymmetric space groups
inferredcites →https://doi.org/10.1039/c1dt10073dopenalex-snapshot
Bridged cyclophosphazenes resulting from deprotonation reactions of cyclotriphophazenes bearing a P–NH group
inferredcites →https://doi.org/10.1039/c1dt10176eopenalex-snapshot
Competitive formation of cis and trans derivatives in the nucleophilic substitution reactions of cyclophosphazenes having a mono-spiro P–NHR group
inferredcites →https://doi.org/10.1039/c2dt31852kopenalex-snapshot
Three novel 3D coordination polymers based on a flexible multisite cyclotetraphosphazene ligand
inferredcites →https://doi.org/10.1039/c6nj00204hopenalex-snapshot
Phosphorus–nitrogen compounds. Part 35. Syntheses, spectroscopic and electrochemical properties, and antituberculosis, antimicrobial and cytotoxic activities of mono-ferrocenyl-spirocyclotetraphosphazenes
inferredcites →https://doi.org/10.1039/c7cc04949hopenalex-snapshot
Phosphorus dendrimers for nanomedicine
inferredcites →https://doi.org/10.1039/c9nj00577copenalex-snapshot
Phosphorus–nitrogen compounds. Part 42. The comparative syntheses of 2- cis -4-ansa(N/O) and spiro(N/O) cyclotetraphosphazene derivatives: spectroscopic and crystallographic characterization, antituberculosis and cytotoxic activity studies
inferredcites →https://doi.org/10.1039/d1nj04585gopenalex-snapshot
Synthesis, characterization and cytotoxic activity studies on cancer cell lines of new paraben-decorated monospiro-cyclotriphosphazenes
inferredcites →https://doi.org/10.1039/dt9870002023openalex-snapshot
Phosphorus–nitrogen compounds. Part 50. Further studies on the formation of bicyclic cyclotetraphosphazatetraene derivatives
inferredcites →https://doi.org/10.1080/10426507.2010.496120openalex-snapshot
Synthesis and Characterization of Side Group–Modified Cyclotetraphosphazene Derivatives
inferredcites →https://doi.org/10.1080/10426507.2016.1160240openalex-snapshot
Synthesis, structural characterization, and cytotoxic activity of new spirocyclic octachlorocyclotetraphosphazenes
inferredcites →https://doi.org/10.1080/10426507.2017.1359595openalex-snapshot
The reactions of 2-trans-6-bis(4-fluorobenzyl)spirocyclotetraphosphazene with primary amines: spectroscopic and crystallographic characterizations
inferredcites →https://doi.org/10.1080/10426507.2018.1469490openalex-snapshot
Syntheses and structural characterizations of 2-pyridyl(N/O)spirocyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1080/10426507.2021.1986502openalex-snapshot
Phosphorus-nitrogen compounds. Part 56. Comparative syntheses and spectral properties of multiheterocyclic 2-cis-4-ansa and spiro-ferrocenyl (N/O)cyclotetraphosphazenes: Antituberculosis and antimicrobial activity and DNA interaction studies
inferredcites →https://doi.org/10.1107/s0021889812029111openalex-snapshot
WinGX and ORTEP for Windows : an update
inferredcites →https://doi.org/10.18596/jotcsa.379971openalex-snapshot
Syntheses and spectroscopic investigations of 2-pyridyl(N/N)spirocyclotriphosphazenes
inferredcites →https://doi.org/10.9767/bcrec.11.2.541.151-160openalex-snapshot
New Method for Nucleophilic Substitution on Hexachlorocyclotriphosphazene by Allylamine Using an Algerian Proton Exchanged Montmorillonite Clay (Maghnite-H+) as a Green Solid Catalyst
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4816439openalex-extracted
Cyclotriphosphazenes: Pre-Harvest Foliar Applications Improve Antioxidant Activity by Increasing Phenolic Compounds in Lavandula Angustifolia Mill
inferred← citeshttps://doi.org/10.1002/aoc.70595openalex-snapshot
Phosphorus‐Nitrogen Compounds. Part 85. Design and Synthesis of Novel Hybrid Multiheterocyclic spiro ‐ and 2‐ cis ‐4‐ ansa ‐Ferrocenyl‐(N/O)‐cyclotetraphosphazene Conjugates Bearing Piperonal Pendant Arms: Structural Characterizations, Carbonic Anhydrase Activation, and Antioxidant Activity Studies
inferred← citeshttps://doi.org/10.1007/s11164-024-05285-7openalex-snapshot
Phosphorus–nitrogen compounds: part 75—design, synthesis, stereogenic and conformational properties of chiral dispiro(N/N)cyclotriphosphazenes: structural analysis and photophysical and bioactivity studies
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.104826openalex-snapshot
Cyclotriphosphazenes: Pre-harvest foliar applications improve antioxidant activity by increasing phenolic compounds in Lavandula angustifolia Mill.
inferred← citeshttps://doi.org/10.1016/j.ica.2025.122836openalex-snapshot
Indolyl-3-spiro(N/N)cyclotriphosphazenes: syntheses, spectral, crystallographic and thermal analyses
inferred← citeshttps://doi.org/10.1016/j.ica.2026.123201openalex-snapshot
Unsymmetrical amine-alcohol functionalization of cyclotetraphosphazenes: structural diversity and spectroscopic investigation
inferred← citeshttps://doi.org/10.1016/j.ica.2026.123444openalex-snapshot
Phosphorus‑nitrogen compounds. Part 88. Design and preparation of fully substituted mono(4-nitrobenzyl)spiro(N/N)cyclotriphosphazenes: Chemical, structural investigation, carbonic anhydrase activation and free radical scavenging activity studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.145126openalex-snapshot
Phosphorus-nitrogen compounds: Part 82. Experimental and computational studies of (p-dimethylamino)benzylspiro-(N/N)-cyclotriphosphazene derivatives
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146671openalex-snapshot
Phosphorus-nitrogen compounds. Part 86. Comparative synthesis of dispiromono and dispirobicyclotetraphosphazenes: Spectral, crystallographic and thermal properties, antimicrobial, antituberculosis and DNA-cleavage activities, antiproliferative effects and 3D tumor modeling studies with cancer stem…
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147815openalex-snapshot
The design of fully and partially substituted indole-functionalized cyclotriphosphazenes: Synthesis, chirality, thermal characterization, antioxidant, and in silico ADME-bioactivity profiling
inferred← citeshttps://doi.org/10.1039/d3nj00721aopenalex-snapshot
Phosphorus–nitrogen compounds: part 70. Syntheses of tetraaminomono/bis(4-fluorobenzyl)spiro( N / N )cyclotriphosphazenes: structural characterization, Hirshfeld surface analysis and comparative evaluation of esterase activities of hCA I and hCA II isoenzymes
inferred← citeshttps://doi.org/10.1039/d6nj00879hopenalex-snapshot
The syntheses, crystal structures, and spectroscopic, chiral, thermal and free radical scavenging properties of fully and partially substituted indolyl-phosphazenes
inferred← citeshttps://doi.org/10.1080/10426507.2022.2145477openalex-snapshot
Phosphorus-nitrogen compounds. Part 67. The reactions of Mono/bis (4-fluorobenzyl)spiro(N/N)cyclotriphosphazenes with sodium(3-amino-1-propanoxide): investigation of spectral properties, DNA-cleavage and antimicrobial activities
inferred← citeshttps://doi.org/10.1080/10426507.2025.2456201openalex-snapshot
Phosphorus-nitrogen compounds. Part 77. The synthesis of novel ferrocenyl(N/O)spiro- and 2- cis -4-dichloro-ferrocenyl(N/O)ansa-cyclotetraphosphazenes with 9-ethyl-3-carbazolyl pendant arm(s): spectral, bioactivity, electrochemical and dye-sensitized solar cell fabrication studies
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