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DNA-Dinucleotides Bearing a 3‘,3‘-Cobalt- or 3‘,3‘-Iron-1,2,1‘,2‘-dicarbollide Complex

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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.200352505openalex-snapshot

A Nucleoside Conjugate Containing a Metallacarborane Group and Its Incorporation into a DNA Oligonucleotide

inferredcites →https://doi.org/10.1002/chem.200600740openalex-snapshot

Nucleoside–Metallacarborane Conjugates for Base‐Specific Metal Labeling of DNA

inferredcites →https://doi.org/10.1016/j.elecom.2006.12.010openalex-snapshot

Nucleoside–metallacarborane conjugates for multipotential electrochemical coding of DNA

inferredcites →https://doi.org/10.1016/s0010-8545(02)00087-5openalex-snapshot

The medicinal chemistry of carboranes

inferredcites →https://doi.org/10.1016/s0923-2508(98)80442-7openalex-snapshot

Methods in molecular biology

inferredcites →https://doi.org/10.1021/bc0498323openalex-snapshot

Sequence-Selective Cleavage of Oligoribonucleotides by 3d Transition Metal Complexes of 1,5,9-Triazacyclododecane-Functionalized 2‘-O-Methyl Oligoribonucleotides

inferredcites →https://doi.org/10.1021/cr0101510openalex-snapshot

Bioorganometallic Chemistry of Ferrocene

inferredcites →https://doi.org/10.1021/ja01086a053openalex-snapshot

Carbametallic Boron Hydride Derivatives. I. Apparent Analogs of Ferrocene and Ferricinium Ion

inferredcites →https://doi.org/10.1070/rc2003v072n06abeh000807openalex-snapshot

Ferrocene-containing nucleic acids. Synthesis and electrochemical properties

inferredcites →https://doi.org/10.1073/pnas.0700316104openalex-snapshot

Synthesis and evaluation of transthyretin amyloidosis inhibitors containing carborane pharmacophores

inferredcites →https://doi.org/10.1135/cccc19970047openalex-snapshot

Dimethyl Sulfate Induced Nucleophilic Substitution of the [Bis(1,2-dicarbollido)-3-cobalt(1-)]ate Ion. Syntheses, Properties and Structures of Its 8,8'-μ-Sulfato, 8-Phenyland 8-Dioxane Derivatives

inferredcites →https://doi.org/10.1139/v73-569openalex-snapshot

The tert-Butyldimethylsilyl Group as a Protecting Group in Deoxynucleosides

inferredcites →https://doi.org/10.1351/pac200375091197openalex-snapshot

Boron clusters for medicinal drug design: Selective estrogen receptor modulators bearing carborane

inferredcites →https://doi.org/10.2174/138527207780059358openalex-snapshot

DNA as Platform for New Biomaterials. Metal-Containing Nucleic Acids

inferredcites →https://doi.org/10.2174/138955707780059808openalex-snapshot

Boronated DNA-Binding Compounds as Potential Agents for Boron Neutron Capture Therapy

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Synthesis of Purine Conjugates with Bis-Carboranyl Derivatives of (S)-Lysine or (S)-Glutamic Acid

inferred← citeshttps://doi.org/10.2139/ssrn.4496950openalex-extracted

Synthesis of Purine Conjugates with Bis-Carboranyl Derivatives of (S)-Lysine or (S)-Glutamic Acid

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Boron: Metallacarbaboranes

inferred← citeshttps://doi.org/10.1002/0471142700.nc0437s38openalex-snapshot

Nucleoside Modification with Boron Clusters and Their Metal Complexes

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Boron: Metallacarbaboranes

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Electronic Tuning of Nickel‐Based Bis(dicarbollide) Redox Shuttles in Dye‐Sensitized Solar Cells

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Expanding the Range of Bioorthogonal Tags for Multiplex Stimulated Raman Scattering Microscopy

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Electronic Tuning of Nickel‐Based Bis(dicarbollide) Redox Shuttles in Dye‐Sensitized Solar Cells

inferred← citeshttps://doi.org/10.1002/anie.202311530openalex-snapshot

Expanding the Range of Bioorthogonal Tags for Multiplex Stimulated Raman Scattering Microscopy

inferred← citeshttps://doi.org/10.1002/cbic.201402611openalex-snapshot

Synthesis of Lysozyme–Metallacarborane Conjugates and the Effect of Boron Cluster Modification on Protein Structure and Function

inferred← citeshttps://doi.org/10.1002/cbic.201500569openalex-snapshot

Charge‐Compensated Metallacarborane Building Blocks for Conjugation with Peptides

inferred← citeshttps://doi.org/10.1002/chin.201217264openalex-snapshot

ChemInform Abstract: Cyclic Oxonium Derivatives as an Efficient Synthetic Tool for the Modification of Polyhedral Boron Hydrides

inferred← citeshttps://doi.org/10.1002/ejic.200900003openalex-snapshot

Polyhedral Boranes for Medical Applications: Current Status and Perspectives

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Metallacarboranes as Labels for Multipotential Electrochemical Coding of DNA. [3‐Chromium bis(dicarbollide)](‐1)ate and Its Nucleoside Conjugates

inferred← citeshttps://doi.org/10.1007/s11172-013-0095-0openalex-snapshot

Synthesis of podands with nido-carboranyl groups as a basis for construction of crown ethers with an incorporated metallacarborane moiety

inferred← citeshttps://doi.org/10.1016/b978-0-08-102688-5.00031-3openalex-snapshot

Metal Complexes in Mechanochemistry

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Carboranes in medicine

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Carboranes in Medicine

inferred← citeshttps://doi.org/10.1016/b978-0-12-820206-7.00030-5openalex-snapshot

Oligonucleotide Complexes in Bioorganometallic Chemistry

inferred← citeshttps://doi.org/10.1016/j.bioelechem.2011.10.005openalex-snapshot

Electrochemical detection of DNA hybridization using metallacarborane unit

inferred← citeshttps://doi.org/10.1016/j.bios.2013.07.026openalex-snapshot

DNA probe modified with 3-iron bis(dicarbollide) for electrochemical determination of DNA sequence of Avian Influenza Virus H5N1

inferred← citeshttps://doi.org/10.1016/j.ejps.2017.09.036openalex-snapshot

Insight into lipophilicity of deoxyribonucleoside‑boron cluster conjugates

inferred← citeshttps://doi.org/10.1016/j.inoche.2009.12.012openalex-snapshot

The ligand-structure-selective binding of oligonucleotide by cobalt complexes

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Practical synthesis of 1,4-dioxane derivative of the closo-dodecaborate anion and its ring opening with acetylenic alkoxides

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2008.12.061openalex-snapshot

Nucleoside–boron cluster conjugates – Beyond pyrimidine nucleosides and carboranes

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.07.005openalex-snapshot

Novel alkoxy derivatives of cobalt bis(1,2-dicarbollide)

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Synthesis and functionalization of nitrosyl rhenacarboranes towards their use as drug delivery vehicles

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.04.006openalex-snapshot

Cobalt bis(dicarbollide) anion and its derivatives

inferred← citeshttps://doi.org/10.1016/j.mencom.2011.03.008openalex-snapshot

New conjugates of cobalt bis(dicarbollide) with chlorophyll a derivatives

inferred← citeshttps://doi.org/10.1016/j.molliq.2025.127232openalex-snapshot

Aggregation of metallacarborane mixtures in aqueous solutions: Iron bis(1,2-dicarbollide) as paramagnetic probe in aggregates of diamagnetic cobalt bis(1,2-dicarbollide)

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2023.108548openalex-snapshot

Boron in cancer therapeutics: An overview

inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154686openalex-snapshot

Synthesis of purine conjugates with bis-carboranyl derivatives of (S)-lysine or (S)-glutamic acid

inferred← citeshttps://doi.org/10.1021/ac801235bopenalex-snapshot

Electrochemical DNA Detection Based on the Polyhedral Boron Cluster Label

inferred← citeshttps://doi.org/10.1021/acsomega.3c00422openalex-snapshot

Two Shared Icosahedral Metallacarboranes through Iron: A Joint Experimental and Theoretical Refinement of Mössbauer Spectrum in [Fe(1,2-C2B9H11)2]Cs

inferred← citeshttps://doi.org/10.1021/ic502450topenalex-snapshot

The Synthesis and Structural Characterization of Polycyclic Derivatives of Cobalt Bis(dicarbollide)(1 – )

inferred← citeshttps://doi.org/10.1021/ja100396nopenalex-snapshot

Ni(III)/(IV) Bis(dicarbollide) as a Fast, Noncorrosive Redox Shuttle for Dye-Sensitized Solar Cells

inferred← citeshttps://doi.org/10.1021/jacs.6c07376openalex-snapshot

Late-Stage Carboranylation of Nucleos(t)ides Enabled by Minisci and Pd-Catalyzed B–N Cross-Coupling Reactions: Toward the Synthesis of Carboranyl-Modified Oligonucleotides

inferred← citeshttps://doi.org/10.1021/om200938nopenalex-snapshot

The Zwitterion [8,8′-μ-CH2O(CH3)-(1,2-C2B9H10)2-3,3′-Co]0 as a Versatile Building Block To Introduce Cobalt Bis(Dicarbollide) Ion into Organic Molecules

inferred← citeshttps://doi.org/10.1038/nchem.1088openalex-snapshot

A coordination chemistry dichotomy for icosahedral carborane-based ligands

inferred← citeshttps://doi.org/10.1039/b715363eopenalex-snapshot

Cyclic oxonium derivatives of polyhedral boron hydrides and their synthetic applications

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Ferrocene-like iron bis(dicarbollide), [3-FeIII-(1,2-C2B9H11)2]−. The first experimental and theoretical refinement of a paramagnetic 11B NMR spectrum

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Direct and facile synthesis of carbon substituted alkylhydroxy derivatives of cobalt bis(1,2-dicarbollide), versatile building blocks for synthetic purposes

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Synthesis, characterisation and some chemistry of C- and B-substituted carboxylic acids of cobalt bis(dicarbollide)

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The effect of a paramagnetic metal ion within a molecule: comparison of the structurally identical paramagnetic [3,3-Fe(1,2-C 2 B 9 H 11 ) 2 ] − with the diamagnetic [3,3-Co(1,2-C 2 B 9 H 11 ) 2 ] − sandwich complexes

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Cyclic oxonium derivatives of cobalt and iron bis(dicarbollides) and their use in organic synthesis

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Metallacarboranes for the labelling of DNA — Synthesis of oligonucleotides bearing a 3,3′-iron-1,2,1′,2′-dicarbollide complex

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Recent Advances in the Synthesis of High Boron-Loaded Nucleic Acids for BNCT

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Interaction of Adenosine, Modified Using Carborane Clusters, with Ovarian Cancer Cells: A New Anticancer Approach against Chemoresistance

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DNA Modified with Boron–Metal Cluster Complexes [M(C2B9H11)2]—Synthesis, Properties, and Applications

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