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Advances and Applications in Deep Eutectic Solvents Technology
| Advances and Applications in Deep Eutectic Solvents Technology |
| Autore | Tiecco Matteo |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 online resource (104 p.) |
| Soggetto topico |
Chemistry
Research and information: general |
| Soggetto non controllato |
absorption
API formulation band gap energy biogas carbon dioxide reduction carbon dioxide transformation deep eutectic solvents Deep Eutectic Solvents design of experiments DESs water dilutions electrochemical conversion eutectic mixtures extraction functionalized ionic liquids (ILs) gas sorbents hydrogen bond acceptor hydrogen bond donor ionothermal synthesis materials organic synthesis preconcentration quercetin recovery renewable energy RP-HPLC-UV siloxanes Tauc plot UHPLC-MS/MS |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910566472503321 |
Tiecco Matteo
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| 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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Molecules from Side Reactions
| Molecules from Side Reactions |
| Autore | D'Errico Stefano |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (100 p.) |
| Soggetto topico | History of engineering and technology |
| Soggetto non controllato |
(E,Z)-isomerization
19F NMR spectroscopy 1H-pyrazolo[3,4-b]pyridine 3-acetyl-2,3-dihydro-1,3,4-oxadiazole 8-Fluoro-2'-deoxyguanosine acadesine AICAR allenic compounds AMPK azaheterocycles benzamides bidentate directing groups bis-chelates C-glycosylation C-H bond functionalization caprazamycins carbohydrate chelation assistance chlorinated nucleosides conjugated diyne copper cyanide cyclization diacetal epoxide ester group migration fluorinated nucleosides fluorination furan glycosyl sulfoxide guanidinium heterocycle hydroxy methylation ketose LAH reduction ligand mannose modified nucleosides muraymycins N-alkylation N-C bond cleavage N'-acetylhydrazide n/a network nitration nucleoside analogues nucleosides organic synthesis oxazole oxetane pent-1,2,3,4-tetraene intermediate phosphoramidite phosphorylation psicose pyridine derivatives pyridine-imidazolium rare sugar rearrangement ribose RORC reaction seven-membered rings solid phase synthesis spiro-oxetane thioglycoside oxidation unexpected iminium cation uridine uronate X-ray structure determination |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910674046603321 |
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D'Errico Stefano
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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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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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Synthesis of Flavonoids or Other Nature-Inspired Small Molecules
| Synthesis of Flavonoids or Other Nature-Inspired Small Molecules |
| Autore | Ribaudo Giovanni |
| Pubbl/distr/stampa | Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 |
| Descrizione fisica | 1 online resource (82 p.) |
| Soggetto topico | Research and information: general |
| Soggetto non controllato |
(+)-camphor
1,2,3-triazole 7-hydroxy-2H-chromen-2-one ADMET aminoquinoline anticancer anticonvulsant activity antidiabetic benzylidene derivative C. dichotoma Clusiaceae coumarin curcumin analog DFT calculation docking flavonoids Garcinia porrecta hybrid compound hydrazone kokosanolide Lansium domesticum lupeol derivative MCF-7 Meliaceae molecular modeling n/a O-acylation reaction organic synthesis Oxone® PDE photophysical properties quercetin semi-synthetic sildenafil steady-state fluorescence technology terpenoid tetranortriterpenoid triterpene onoceranoid valproic acid xanthone α-amylase α-glucosidase α-glucosidase inhibition |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557615703321 |
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Ribaudo Giovanni
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| Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances
| Synthesis of Marine Natural Products and Molecules Inspired by Marine Substances |
| Autore | Manzo Emiliano |
| Pubbl/distr/stampa | Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
| Descrizione fisica | 1 online resource (147 p.) |
| Soggetto topico | Language and Linguistics |
| Soggetto non controllato |
7-deazapurine nucleoside
alkylglycerol (AKG) amides/esters antibacterial iminosugars antibiotics (gentamicin antimicrobial activity antiproliferative activity apoptosis aureol bioactive diterpenes bis-indoles breast cancer carbohydrates cholesterol ciprofloxacin and ampicillin) COVID-19 cytostatic disaccharide nucleoside fluoro olefin fucose fucosylated chondroitin sulfate G0/G1 cell-cycle arrest glycosylation HDAC inhibitors labdane scaffold largazole lipophilic iminosugars marine natural product marine-inspired meroterpenoids modification n/a natural product natural products synthesis organic synthesis polymer-supported triphenyl phosphine polysaccharides ricinoleic acid (RA) SARS-CoV-2 sclareolide semi-synthesis solid tumor cell lines structure-activity relationship (SAR) studies structure-activity relationships sulfation synthesis tetracyclic meroterpenoids tetracycline thiazinoquinones total synthesis TRPV4 channel tubercidin |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910557681103321 |
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Manzo Emiliano
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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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