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