Search results for "Iodination"

showing 3 items of 3 documents

Synthesis of quadruped-shaped polyfunctionalized o-carborane synthons

2011

[EN] o-Carborane derivatives with precisely defined patterns of substitution have been prepared from 8,9,10,12-I-4-1,2-closo-C2B10H8 by replacing the iodine atoms, bonded to four adjacent boron vertices in the cluster, with allyl, and subsequently 3-hydroxypropyl groups. The resulting structures, comprising four pendant arms and two reactive vertices located on opposite sides of a central o-carborane core, can be envisaged as versatile precursors for dendritic growth

DendrimersIcosahedral CarboranesStereochemistryMolecular ConformationNeutron-Capture TherapySupramolecular Assemblieschemistry.chemical_elementBoranesCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMolecular conformationDendrimerQUIMICA ANALITICAMaterials ChemistryCluster (physics)BoranesBoronta116CancerIodination010405 organic chemistryChemistryPolysubstituted FrameworksSynthonMetals and AlloysHalogenationGeneral Chemistry3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsC-HChemistryCrystallographyCeramics and CompositesCarboraneDerivativesIodineChemical Communications
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Iodofluorination of alkenes and alkynes promoted by iodine and 4-iodotoluene difluoride

2006

It was found that a mixt. of mol. iodine and 4-iodotoluene difluoride are useful to generate in situ the electrophilic iodine/nucleophilic fluorine (IF) couple that was able to add in a Markovnikov fashion and with prevalent anti-stereoselectivity to various alkenes and alkynes.

Settore AGR/13 - Chimica AgrariaOrganic ChemistryDifluorideMarkovnikov's ruleHalogenationchemistry.chemical_elementGeneral MedicineIodineBiochemistrychemistryDrug DiscoveryPolymer chemistryOrganic chemistryHypervalent iodineElectrophilic iodinationFluoroiodoalkanesFluoroiodoalkenesTetrahedron Letters
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Poly-iodinated closo 1,2-C 2 B 10 and nido [7,8-C 2 B 9 ] − carborane frameworks: Synthesis and consequences

2015

Abstract The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their chemical shift position in the 1H NMR, and the lesser tendency to η5-coordination in parallel to a larger number of iodo groups.

carboranesSolvent freeStereochemistryChemistryOrganic ChemistryHalogenationsolvent freeBiochemistryInorganic ChemistryiodinationMaterials ChemistryProton NMRCarboranePhysical and Theoretical Chemistryta116acidityJournal of Organometallic Chemistry
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