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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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Enzyme-Mediated Stereoselective Synthesis
| Enzyme-Mediated Stereoselective Synthesis |
| Autore | Serra Stefano |
| Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
| Descrizione fisica | 1 online resource (116 p.) |
| Soggetto topico | Chemistry |
| Soggetto non controllato |
?-transaminases
1 1-phenylethanol 4-diols agro-industrial side stream alcohol dehydrogenases alcohol-dehydrogenase aroma compounds asymmetric synthesis biocatalysis bioreduction Burkholderia cepacia lipase chiral amines chiral resolution cyclization diketones enantioselective synthesis enantioselectivity enzyme-mediated resolution esters flavors hydratase hydroxy fatty acids immobilization kinetic resolution Lactobacillus rhamnosus lactones linalool linaloyl oxide linoleic acid linolenic acid linseed cake lipases monoterpenes multi-enzymatic cascades n/a nitroketone oleic acid protein engineering pullulan rapeseed cake reaction engineering reduction solid-state fermentation stereoselective biotransformation |
| ISBN | 3-03921-937-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910367738803321 |
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Serra Stefano
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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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