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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 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
Opac: Controlla la disponibilità qui
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 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
Opac: Controlla la disponibilità qui