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Amide Bond Activation / Michal Szostak
| Amide Bond Activation / Michal Szostak |
| Autore | Szostak Michal |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
| Descrizione fisica | 1 electronic resource (466 p.) |
| Soggetto topico | Chemistry |
| Soggetto non controllato |
N-heterocyclic carbene
non planar amide ruthenium (Ru) physical organic chemistry gemcitabine prodrug pyramidal amides bridged sultams catalysis dipeptides N-(1-naphthyl)acetamide C-N ? bond cleavage steric effects peptide bond cleavage transition-metal-free palladium N-heterocyclic carbenes (NHCs) addition reaction C–O activation rhodium metal complexes carbanions thioamidation amide bond intramolecular catalysis antiviral activity additivity principle pre-catalysts C–N bond cleavage bridged lactams C–H acidity arynes twisted amides organic synthesis amination Suzuki-Miyaura tert-butyl cyclopentadienyl complexes C-S formation enzymes DFT study sulfonamide bond N HERON reaction primaquine entropy amide activation amidation synthesis amide hydrolysis carbonylicity amide bond activation amide bond resonance aminosulfonylation molecular dynamics model compound in situ amide homogeneous catalysis heterocycles anomeric effect multi-component coupling reaction kinetic excited state C–H bond cleavage palladium catalysis amides thiourea formylation alkynes cis/trans isomerization amide C–N bond activation intein C-H functionalization succindiamide amide bonds crown ether aminoacylation directing groups cytostatic activity reaction thermodynamics acyl transfer transition metals N-dimethylformamide DMAc acylative cross-coupling C-H/C-N activation nickel catalysis antibacterial screening sodium aryl thioamides Winkler-Dunitz parameters catalyst N-dimethylacetamide base-catalyed hydrolysis nitrogen heterocycles cross-coupling insertion amidicity nitro-aci tautomerism activation carbonylation transamidation amine distortion Pd-catalysis rotational barrier energy hypersensitivity N–C activation metabolic stability [2+2+2] annulation twisted amide protease cyanation amide resonance trialkylborane catalysts biofilm eradication pharmacokinetics pancreatic cancer cells DMF aryl esters Michael acceptor fumardiamide water solvation ester bond activation cyclization nuclear magnetic resonance secondary amides reaction mechanism density functional theory density-functional theory amino acid transporters |
| ISBN |
9783039212040
3039212044 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910346843703321 |
Szostak Michal
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| MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Recent Advances in Iron Catalysis
| Recent Advances in Iron Catalysis |
| Autore | Knölker Hans-Joachim |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (224 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
alcohols
aldehyde alkenyl halides alkylation amidation amides amines aryl esters asymmetric catalysis asymmetric transfer hydrogenation ate iron(II) complex ATRP bifunctional catalyst BINOL synthesis bis-(aryl)manganese borylation C-C coupling C-H activation C-H functionalisation C-H functionalization C-O activation carbene carboazidation catalysis cinnamamide controlled radical polymerization cross-coupling decarbonylation dehydrogenative coupling density functional theory DFT diazoalkane esters external stimuli Fe-catalysis FeI/FeII/FeIII mechanism fluorescence Grignard reagent haloalkane coupling hydrogen transfer iron Iron iron catalysis iron catalyst iron complexes iron-catalysis iron(III) chloride Kumada cross-coupling naphthidines nitrogen ligand organic synthesis oxidative coupling photochemistry pinacolborane radical reductive amination solvent-free spirocyclization sustainability α-alkenylation β-methyl scission |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557556003321 |
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Knölker Hans-Joachim
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Supramolecular Gold Chemistry : From Atomically Precise Thiolate-Protected Gold Nanoclusters to Gold-Thiolate Nanostructures
| Supramolecular Gold Chemistry : From Atomically Precise Thiolate-Protected Gold Nanoclusters to Gold-Thiolate Nanostructures |
| Autore | Antoine Rodolphe |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (182 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
3-MBA/Au MPCs
6-aza-2-thio-thymine A3−coupling alloy amino acids atomically precise Au-GO nano-hybrid Au(I)-thiolate Au70S20(PPh3)12 cluster bidentate binding catalyst catalytic mechanism catenane cluster coordination polymer coordination polymer structure cross-coupling DFT calculations electron dynamics electronic structure ESI-MS fluorescence fuel cells geometric structure gold gold nanocluster gold nanoclusters gold nanohybrid materials gold nanomaterials gold nanoparticles gold thiolate graphene oxide HPLC-MS hydrogen evolution reaction interface state ion mobility lamellar structure laser ablation ligand effect ligand removal ligand-protected luminescence metal exchange metal nanoclusters n/a nanocatalysis optical properties oxygen evolution reaction oxygen reduction reaction p band intermediate state (PBIS) phonon dynamics photoluminescence mechanism polymer composite protein quantum confinement effect Sonogashira coupling superatom network model Suzuki coupling TEA-HFIP template-assisted synthesis thiolate Ullmann hetero-coupling water splitting |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Supramolecular Gold Chemistry |
| Record Nr. | UNINA-9910557146903321 |
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Antoine Rodolphe
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Transition Metal Catalyzed Cross-Coupling Reactions
| Transition Metal Catalyzed Cross-Coupling Reactions |
| Autore | Kostas Ioannis |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (88 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
alkylboron reagents
alkynyl ketone synthesis alpha-helix anode Buchwald-Hartwig reaction C(sp3) -C(sp2) CH-activation cross-coupling cross-coupling reaction deposited catalysts electrosynthesis functional amides Heck reaction Kumada reaction metal catalysis metal complex n/a oligoarene palladium peptidomimetics phenol protein-protein interactions Sonogashira reaction Suzuki reaction Suzuki-Miyaura cross-couplings thiosemicarbazone transition metal catalysis triflate |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557308403321 |
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Kostas Ioannis
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| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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