Enzyme-Mediated Stereoselective Synthesis |
Autore | Serra Stefano |
Pubbl/distr/stampa | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
Descrizione fisica | 1 electronic resource (116 p.) |
Soggetto non controllato |
enantioselective synthesis
flavors hydroxy fatty acids chiral amines diketones esters oleic acid Burkholderia cepacia lipase multi-enzymatic cascades solid-state fermentation biocatalysis agro-industrial side stream rapeseed cake enzyme-mediated resolution linolenic acid stereoselective biotransformation lipases kinetic resolution 1-phenylethanol linseed cake bioreduction Lactobacillus rhamnosus alcohol-dehydrogenase enantioselectivity hydratase reaction engineering immobilization ?-transaminases linoleic acid cyclization monoterpenes 1 lactones protein engineering asymmetric synthesis alcohol dehydrogenases linaloyl oxide chiral resolution aroma compounds 4-diols pullulan linalool reduction nitroketone |
ISBN | 3-03921-937-5 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910367738803321 |
Serra Stefano | ||
MDPI - Multidisciplinary Digital Publishing Institute, 2019 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
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 electronic resource (120 p.) |
Soggetto topico | Research & information: general |
Soggetto non controllato |
nitro
pyridone 1-methyl-2-quinolone cycloaddition direct functionalization perylenediimide nitro group organic materials Phenacylation of beta-nitropyridin-2-ones 8-nitro-5-RO-indolizines oxazole-pyrrole ring transformation conjugate addition dihydrofuran 1,3-dicarbonyl compound enolate isoxazoline N-oxide nitroketone nitronate nucleophilic substitution nitropyridines isoxazolo[4,3-b]pyridines 1,4-dihydropyridines nucleophilic addition Diels-Alder reaction dearomatization hexapyrrolohexaazacoronene nitration SNAr substitution ICT character aromaticity C–H functionalization total synthesis pyrrolidines anchimeric assistance epimerization PDE4 inhibitors 1,3-Dipole electron-withdrawing ability electrophilicity nucleophilicity |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910557494003321 |
Nishiwaki Nagatoshi | ||
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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