Search results for "Terphenyl"

showing 4 items of 164 documents

A sigma-donor with a planar six-pi-electron B2N2C2 framework: anionic N-heterocyclic carbene or heterocyclic terphenyl anion?

2006

chemistry.chemical_elementAromaticityGeneral ChemistryElectronGeneral MedicinePhotochemistryCatalysisIonchemistry.chemical_compoundPlanarchemistryTerphenylPolymer chemistryLithiumBoronCarbeneAngewandte Chemie (International ed. in English)
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CCDC 1573804: Experimental Crystal Structure Determination

2017

Related Article: Paul J. Ragogna, Cameron Graham, Clement Millet, Amy N Price, Juuso Valijus, Michael J Cowley, Heikki Tuononen|2017|Chem.-Eur.J.|24|672|doi:10.1002/chem.201704337

chloro-{1-[2-(121416323436-hexamethyl[1121:2331-terphenyl]-22-yl)-3-(246-tri-t-butylphenyl)-1234-selenadiphosphaboretan-4-yl]-2266-tetramethylpiperidine}-gold(i) acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Synthesis of novel fluorinated building blocks and α-helix peptidomimetics

2018

At its heart, the present PhD thesis is based on the premise of two important areas in modern organic chemistry: firstly, the development of new methodologies to incorporate fluorine into organic molecules; and secondly, the design and synthesis of small molecules with high therapeutic potential. The work presented in the first three chapters will therefore focus on the incorporation of fluorine into organic molecules and the synthesis of fluorinated building blocks. In each chapter, we aim to obtain biologically relevant small molecules containing fluorine atoms or fluorinated groupings. The introduction of fluorine is a commonly used method in drug discovery to fine-tune the properties of…

fluorinepeptidomimeticsterphenyl:QUÍMICA::Química orgánica [UNESCO]UNESCO::QUÍMICA::Química orgánicaorganic synthesis
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Reactions of m-Terphenyl-Stabilized Germylene and Stannylene with Water and Methanol: Oxidative Addition versus Arene Elimination and Different React…

2015

Reactions of the divalent germylene Ge(ArMe6)2 (ArMe6 = C6H3-2,6-{C6H2-2,4,6-(CH3)3}2) with water or methanol gave the Ge(IV) insertion product (ArMe6)2Ge(H)OH (1) or (ArMe6)2Ge(H)OMe (2), respectively. In contrast, its stannylene congener Sn(ArMe6)2 reacted with water or methanol to produce the Sn(II) species {ArMe6Sn(μ-OH)}2 (3) or {ArMe6Sn(μ-OMe)}2 (4), respectively, with elimination of ArMe6H. Compounds 1–4 were characterized by IR and NMR spectroscopy as well as by X-ray crystallography. Density functional theory calculations yielded mechanistic insight into the formation of (ArMe6)2Ge(H)OH and {ArMe6Sn(μ-OH)}2. The insertion of an m-terphenyl-stabilized germylene into the O–H bond was…

oxidative additionMetathesisPhotochemistryDFT calculationsMedicinal chemistryReductive eliminationInorganic Chemistrychemistry.chemical_compoundTerphenylreaktiomekanismiReactivity (chemistry)metallylenesarene eliminationPhysical and Theoretical Chemistryta116Chemistryareenin eliminaatioArylOrganic ChemistryNuclear magnetic resonance spectroscopyOxidative additionmetallyleenitDFT laskutMethanolreaction mechanismhapettava additioOrganometallics
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