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Showing 1 to 8 of 8 for “"⍺-C–H Functionalisation"”.

  1. Metal-free C-H functionalisation methods

    … describes the development of two metal-free C–H functionalisation methods which encompass oxidations of sp³- and sp²-hybridised C–H bonds.Chapter 1 provides a brief introduction to the rapidly growing area of C–H functionalisation and outlines selected metal-catalysed and metal-free C–H …

    strathclyde Repository record for Metal-free C-H functionalisation methods (opens in a new tab)

  2. Direct ⍺-C–H Functionalisation of Cyclic Alkylamines

    … Consequently, methods for the selective functionalisation of these scaffolds would greatly facilitate the optimisation of biological activity, physicochemical properties and the systematic evaluation of structure-activity relationships. This thesis describes efforts towards the development …

    cambridge Repository record for Direct ⍺-C–H Functionalisation of Cyclic Alkylamines (opens in a new tab)

  3. A concise and scalable total synthesis of dictyodendrin B by sequential C–H functionalisation

    … towards achieving this goal via a sequential C–H functionalisation strategy (Scheme 1). The functionalisation of C–H bonds has attracted considerable interest due to its potential impact on the synthesis of complex molecules. Our aim was to demonstrate the advantages and feasibility of performing …

    cambridge Repository record for A concise and scalable total synthesis of dictyodendrin B by sequential C–H functionalisation (opens in a new tab)

  4. Palladium(II)-Catalysed sp 3 C–H Functionalisation of Hindered Amines and its Application in Synthesis of Astemizole Analogues

    … building blocks. The sterically promoted C–H functionalisation strategy has been employed as the key step in the synthesis of a functionalised analogue of astemizole, a pharmaceutical agent which suffers from undesired hERG activity. The increased steric bulk around the tertiary amine, coupled …

    cambridge Repository record for Palladium(II)-Catalysed sp 3 C–H Functionalisation of Hindered Amines and its Application in Synthesis of Astemizole Analogues (opens in a new tab)

  5. Studies in palladium and rhodium catalysis: synthetic strategies for C–C bond formation

    … wellestablished conditions, which promote C−H functionalisation through Concerted MetalationDeprotonation (CMD), proved unsatisfactory for electron-rich diarylether precursors. Herein, we report a Pd-catalysed C−H functionalisation protocol that works with electron-rich arenes. We suspect that …

    cork Repository record for Studies in palladium and rhodium catalysis: synthetic strategies for C–C bond formation (opens in a new tab)

  6. Controlling Site-Selectivity in Palladium-Catalysed Cross-Coupling Reactions using Non-Covalent Interactions Between Ligand and Substrate

    … used in conjunction with palladium-catalysed C-H functionalisation. Finally, by systematically changing the size of the cation and the position of the sulfonate group on the ligand scaffold, it was possible to achieve site-selective Suzuki coupling of isomeric di-, tri- and tetra-chlorinated …

    cambridge Repository record for Controlling Site-Selectivity in Palladium-Catalysed Cross-Coupling Reactions using Non-Covalent Interactions Between Ligand and Substrate (opens in a new tab)

  7. Late stage oxidative C(sp3)–H alkylation and arylation

    Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2024-05-01

    uiuc Repository record for Late stage oxidative C(sp3)–H alkylation and arylation (opens in a new tab)

  8. Development of Ion Pairing Strategies that Utilise Cations to Control Selectivity in Transition Metal-Catalysed Functionalisation of C–H Bonds

    … The formidable challenge of selective C–H bond functionalisation through transition metal catalysis offers an ideal platform to investigate the potential of invoking control through ion pairing interactions. The ion pairing strategies explored in this thesis focus on how cations may be used to …

    cambridge Repository record for Development of Ion Pairing Strategies that Utilise Cations to Control Selectivity in Transition Metal-Catalysed Functionalisation of C–H Bonds (opens in a new tab)