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Advances in Cross-Coupling Reactions
| Advances in Cross-Coupling Reactions |
| Autore | Pérez Sestelo José |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (234 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
2,3'-bipyrrole
5-aryl pyrrole-2-carboxylates acylation Al2O3 allosteric modulators arenes borylated aryl alkynes borylation C-C bond forming reactions C-C cross-coupling C-H activation C-H borylation C-H functionalization C-Heteroatom bond forming reactions catalysis in water clinical candidate cross coupling cross-coupling reactions cyclopeptides dearomatization dimerization and trimerization of indoles DNA-encoded libraries DSSC electrophilic haloacetylenes ethynylpyrroles furans Heck reaction heteroarenes heteroaryl substituted pyrroles indigo dyes indolin-3-ones intramolecular cyclization iridium-catalyzed M(CO)3 tripods medium-sized heterocycles methoxycarbonylation molecular brakes and gears n/a NH-Free one-pot reaction palladium profene PROTAC pyrazoles pyrroles restricted rotations Sonogashira cross-coupling spectroscopy styrene sulfonated salan Suzuki coupling Suzuki-Miyaura reaction synthesis thiophenes transition-metal catalysis V-T NMR X-ray |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557316703321 |
Pérez Sestelo José
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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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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 |
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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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Nitro Compounds and Their Derivatives in Organic Synthesis
| Nitro Compounds and Their Derivatives in Organic Synthesis |
| Autore | Nishiwaki Nagatoshi |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 |
| Descrizione fisica | 1 online resource (120 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
1-methyl-2-quinolone
1,3-dicarbonyl compound 1,3-Dipole 1,4-dihydropyridines 8-nitro-5-RO-indolizines anchimeric assistance aromaticity C-H functionalization conjugate addition cycloaddition dearomatization Diels-Alder reaction dihydrofuran direct functionalization electron-withdrawing ability electrophilicity enolate epimerization hexapyrrolohexaazacoronene ICT character isoxazoline N-oxide isoxazolo[4,3-b]pyridines nitration nitro nitro group nitroketone nitronate nitropyridines nucleophilic addition nucleophilic substitution nucleophilicity organic materials oxazole-pyrrole ring transformation PDE4 inhibitors perylenediimide Phenacylation of beta-nitropyridin-2-ones pyridone pyrrolidines SNAr substitution total synthesis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557494003321 |
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Nishiwaki Nagatoshi
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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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Organic Synthesis via Transition Metal-Catalysis
| Organic Synthesis via Transition Metal-Catalysis |
| Autore | Gabriele Bartolo |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 electronic resource (144 p.) |
| Soggetto topico | Research & information: general |
| Soggetto non controllato |
palladium
indole indomethacin C-H functionalization sulfoximide C-H activation benzothiazine rhodium catalysis synthesis organosulfur compounds S-S bond cleavage chemical equilibrium reversible reaction alkynes annulation benzimidazoxazinones heterocycles polycyclic heterocycles heterocyclization zinc direct arylation pincer complexes vanadium(IV) complexes biological activity catalytic properties 8-hydroxyquinoline cytotoxicity studies hydroformylation hydrogenation tandem reaction |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557611103321 |
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Gabriele Bartolo
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| 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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