Boron‐Based Compounds 2018
DOI: 10.1002/9781119275602.ch1.4
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Half‐ and Mixed‐Sandwich Transition Metal Dicarbollides andnido‐Carboranes(–1) for Medicinal Applications

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Cited by 7 publications
(7 citation statements)
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“…82 Additionally, both ferrabis(dicarbollide) moieties were tested in terms of their application in PBCT, which besides BNCT carries a great potential for aggressive glioblastoma treatment. In the first step of reaction underlying PBCT, an 11 B isotope fuses with a proton yielding an excited state carbon nucleus 12 C, which decays to a single α particle and a beryllium nucleus 8 Be further decaying to two additional alpha particles. This, in theory, results in the generation of a 3-fold higher alpha particles number per reaction than the BNCT 83 (the comparison between these reactions is pictured in Figure 6).…”
Section: Venus Flytrap Cluster As a Stablementioning
confidence: 99%
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“…82 Additionally, both ferrabis(dicarbollide) moieties were tested in terms of their application in PBCT, which besides BNCT carries a great potential for aggressive glioblastoma treatment. In the first step of reaction underlying PBCT, an 11 B isotope fuses with a proton yielding an excited state carbon nucleus 12 C, which decays to a single α particle and a beryllium nucleus 8 Be further decaying to two additional alpha particles. This, in theory, results in the generation of a 3-fold higher alpha particles number per reaction than the BNCT 83 (the comparison between these reactions is pictured in Figure 6).…”
Section: Venus Flytrap Cluster As a Stablementioning
confidence: 99%
“…However, these two ligands show differences in charge and organometallic symmetry they make. 10,12 As a result, the character of the aromacity is different for both moieties: metallacarboranes display global aromaticity, whereas metallocenes present local aromaticity only in the ligands. 13 Therefore, metallacarboranes present a completely different set of physical, chemical, and biological properties than the corresponding cyclopentadienyl-based metallocenes.…”
Section: Introductionmentioning
confidence: 99%
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“…Thus, the development of drugs in which the carborane moiety mimics a phenyl group or is the pharmacophore itself is actively studied [23][24][25][26][27][28][29]. Applications of such carborane-containing drugs are for example cancer therapeutics and enzyme inhibitors [11,14,19,20,22,23,[30][31][32][33][34][35][36][37]. Due to its isolobal relationship with the cyclopentadienyl ligand (Cp − ) the dicarbollide anion (nido-carborate(2−), C2B9H11 2− , Cb 2− ) is a suitable replacement as ligand for transition metals [38,39].…”
Section: Introductionmentioning
confidence: 99%