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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 |
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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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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