Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Amide Bond Activation
| Amide Bond Activation |
| Autore | Szostak Michal |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
| Descrizione fisica | 1 electronic resource (466 p.) |
| 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 | 3-03921-204-4 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910346843703321 |
Szostak Michal
|
||
| MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
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 electronic resource (224 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
iron
cross-coupling aryl esters C–O activation Fe-catalysis Kumada cross-coupling iron complexes hydrogen transfer reductive amination alcohols amines decarbonylation alkylation spirocyclization aldehyde cinnamamide iron catalysis bis-(aryl)manganese alkenyl halides ate iron(II) complex asymmetric catalysis nitrogen ligand oxidative coupling BINOL synthesis carbene diazoalkane C-H functionalization catalysis borylation Iron C-H functionalisation pinacolborane photochemistry amidation iron(III) chloride amides esters solvent-free iron-catalysis carboazidation β-methyl scission radical DFT organic synthesis C-H activation C-C coupling α-alkenylation dehydrogenative coupling sustainability naphthidines fluorescence iron catalyst ATRP controlled radical polymerization external stimuli asymmetric transfer hydrogenation density functional theory bifunctional catalyst haloalkane coupling Grignard reagent FeI/FeII/FeIII mechanism |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557556003321 |
|
Knölker Hans-Joachim
|
||
| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
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 electronic resource (182 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
alloy
metal exchange atomically precise gold nanoclusters thiolate catenane ion mobility DFT calculations gold nanocluster cross-coupling Ullmann hetero-coupling Sonogashira coupling Suzuki coupling A3−coupling catalytic mechanism ligand removal gold nanomaterials electron dynamics phonon dynamics optical properties Au70S20(PPh3)12 cluster superatom network model electronic structure geometric structure gold nanoparticles graphene oxide laser ablation Au-GO nano-hybrid coordination polymer structure amino acids template-assisted synthesis fluorescence Au(I)-thiolate gold nanohybrid materials 3-MBA/Au MPCs TEA-HFIP ESI-MS HPLC-MS bidentate binding gold thiolate coordination polymer lamellar structure luminescence polymer composite gold cluster catalyst hydrogen evolution reaction oxygen evolution reaction oxygen reduction reaction water splitting fuel cells ligand-protected photoluminescence mechanism metal nanoclusters quantum confinement effect ligand effect p band intermediate state (PBIS) interface state nanocatalysis 6-aza-2-thio-thymine protein |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Supramolecular Gold Chemistry |
| Record Nr. | UNINA-9910557146903321 |
|
Antoine Rodolphe
|
||
| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
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 electronic resource (88 p.) |
| Soggetto topico | Technology: general issues |
| Soggetto non controllato |
Suzuki-Miyaura cross-couplings
C(sp3) -C(sp2) alkylboron reagents metal catalysis alpha-helix anode CH-activation cross-coupling electrosynthesis oligoarene peptidomimetics phenol protein-protein interactions triflate thiosemicarbazone metal complex transition metal catalysis cross-coupling reaction Heck reaction Suzuki reaction Sonogashira reaction Kumada reaction Buchwald-Hartwig reaction deposited catalysts palladium functional amides alkynyl ketone synthesis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557308403321 |
|
Kostas Ioannis
|
||
| Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||