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Alkaline oxidation of enzymatic hydrolysis lignin using reversibly soluble bases / / Jacob S. Kruger [and five others]
| Alkaline oxidation of enzymatic hydrolysis lignin using reversibly soluble bases / / Jacob S. Kruger [and five others] |
| Autore | Kruger Jacob S. |
| Pubbl/distr/stampa | [Golden, Colo.] : , : National Renewable Energy Laboratory, , [2021] |
| Descrizione fisica | 1 online resource (18 pages) : color illustrations |
| Collana | NREL/PR |
| Soggetto topico |
Hydrolysis
Lignin |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910717032203321 |
Kruger Jacob S.
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| [Golden, Colo.] : , : National Renewable Energy Laboratory, , [2021] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Biofuels as an alternative energy source for aviation [[electronic resource] ] : a survey / / Bilal M. McDowell Bomani ... [and others]
| Biofuels as an alternative energy source for aviation [[electronic resource] ] : a survey / / Bilal M. McDowell Bomani ... [and others] |
| Pubbl/distr/stampa | Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , [2009] |
| Descrizione fisica | 1 online resource (16 pages) : illustrations |
| Altri autori (Persone) | BomaniBilal M. McDowell |
| Collana | NASA TM- |
| Soggetto topico |
Ethyl alcohol
Fossil fuels Renewable energy Synthetic fuels Bioconversion Hydrolysis Fuel oils |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Biofuels as an alternative energy source for aviation |
| Record Nr. | UNINA-9910696936203321 |
| Cleveland, Ohio : , : National Aeronautics and Space Administration, Glenn Research Center, , [2009] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction
| Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction |
| Autore | Roberts Stanley M |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2003 |
| Descrizione fisica | 1 online resource (245 p.) |
| Disciplina |
660.634
660/.28443 |
| Altri autori (Persone) | PoignantGeraldine |
| Collana | Catalysts For Fine Chemicals Synthesis |
| Soggetto topico |
Catalysts
Chemistry, Organic Enzymes Hydrolysis Organic compounds Oxidation-reduction reaction Synthesis Biomedical Engineering Health & Biological Sciences |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-27032-2
9786610270323 0-470-36296-0 0-470-85579-7 0-470-85580-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalysts for Fine Chemical Synthesis Volume 1; Contents; Series Preface; Preface to Volume 1; Abbreviations; PART I: REVIEW; 1 The Integration of Biotransformations into the Catalyst Portfolio; 1.1 Hydrolysis of esters, amides, nitriles and oxiranes; 1.2 Reduction reactions; 1.2.1 Reduction of carbonyl compounds; 1.2.2 Reduction of alkenes; 1.3 Oxidative transformations; 1.4 Carbon-carbon bond-forming reactions; 1.5 Conclusions; References; PART II: PROCEDURES; 2 General Information; 3 Asymmetric Epoxidation; 3.1 Introduction; References; 4 Epoxidation of a, b-Unsaturated Carbonyl Compounds
4.1 Non-asymmetric epoxidation4.2 Asymmetric epoxidation using poly-D-leucine; 4.2.1 Synthesis of leucine N-carboxyanhydride; 4.2.2 Synthesis of immobilized poly-D-leucine; 4.2.3 Asymmetric epoxidation of (E)-benzylideneacetophenone; 4.2.4 Conclusion; 4.3 Asymmetric epoxidation using chiral modified diethylzinc; 4.3.1 Epoxidation of 2-isobutylidene-1-tetralone; 4.3.2 Conclusion; 4.4 Asymmetric epoxidation of (E)-benzylideneacetophenone using the La-(R)-BINOL-Ph(3)PO/cumene hydroperoxide system; 4.4.1 Merits of the system; References; 5 Epoxidation of Allylic Alcohols 5.1 Non-asymmetric epoxidation5.2 Asymmetric epoxidation using a chiral titanium complex; 5.2.1 Epoxidation of cinnamyl alcohol; 5.2.2 Epoxidation of (E)-2-methyl-3-phenyl-2-propenol; 5.2.3 Epoxidation of (E)-2-hexen-1-ol; 5.2.4 Conclusion; 5.3 Asymmetric epoxidation of (E)-undec-2-en-1-ol using poly(octamethylene tartrate); 5.3.1 Synthesis of branched poly (octamethylene-L-(+)-tartrate); 5.3.2 Asymmetric epoxidation of (E)-undec-2-en-1-ol; References; 6 Epoxidation of Unfunctionalized Alkenes and a, b-Unsaturated Esters 6.1 Asymmetric epoxidation of disubstituted Z-alkenes using a chiral salen-manganese complex6.1.1 Epoxidation of (Z)-methyl styrene; 6.1.2 Epoxidation of (Z)-ethyl cinnamate; 6.1.3 Conclusion; 6.2 Asymmetric epoxidation of disubstituted E-alkanes using a D-fructose based catalyst; 6.2.1 Epoxidation of (E)-stilbene; 6.2.2 Conclusion; 6.3 Enantioselective epoxidation of (E)-b-methylstyrene by D(2)-symmetric chiral trans-dioxoruthenium (VI) porphyrins; 6.3.1 Preparation of the trans-dioxoruthenium(VI) complexes with D(2)-symmetric porphyrins (H(2)L(1-3)) 6.3.2 Enantioselective epoxidation of (E)-b-methylstyrene6.3.3 Conclusion; References; 7 Asymmetric Hydroxylation and Aminohydroxylation; 7.1 Asymmetric aminohydroxylation of 4-methoxystyrene; 7.1.1 Conclusion; 7.2 Asymmetric dihydroxylation of (1-cyclohexenyl)acetonitrile; 7.2.1 (R,R)-(1,2-Dihydroxycyclohexyl)acetonitrile acetonide; 7.2.2 Conclusion; References; 8 Asymmetric Sulfoxidation; 8.1 Asymmetric oxidation of sulfides and kinetic resolution of sulfoxides; 8.1.1 Asymmetric oxidation of 4-bromothioanisole; 8.1.2 Kinetic resolution of racemic 4-bromophenyl methyl sulfoxide; References 9 Asymmetric Reduction of Ketones Using Organometallic Catalysts |
| Record Nr. | UNINA-9910143508003321 |
|
Roberts Stanley M
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| Hoboken, : Wiley, 2003 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction
| Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction |
| Autore | Roberts Stanley M |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2003 |
| Descrizione fisica | 1 online resource (245 p.) |
| Disciplina |
660.634
660/.28443 |
| Altri autori (Persone) | PoignantGeraldine |
| Collana | Catalysts For Fine Chemicals Synthesis |
| Soggetto topico |
Catalysts
Chemistry, Organic Enzymes Hydrolysis Organic compounds Oxidation-reduction reaction Synthesis Biomedical Engineering Health & Biological Sciences |
| ISBN |
1-280-27032-2
9786610270323 0-470-36296-0 0-470-85579-7 0-470-85580-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalysts for Fine Chemical Synthesis Volume 1; Contents; Series Preface; Preface to Volume 1; Abbreviations; PART I: REVIEW; 1 The Integration of Biotransformations into the Catalyst Portfolio; 1.1 Hydrolysis of esters, amides, nitriles and oxiranes; 1.2 Reduction reactions; 1.2.1 Reduction of carbonyl compounds; 1.2.2 Reduction of alkenes; 1.3 Oxidative transformations; 1.4 Carbon-carbon bond-forming reactions; 1.5 Conclusions; References; PART II: PROCEDURES; 2 General Information; 3 Asymmetric Epoxidation; 3.1 Introduction; References; 4 Epoxidation of a, b-Unsaturated Carbonyl Compounds
4.1 Non-asymmetric epoxidation4.2 Asymmetric epoxidation using poly-D-leucine; 4.2.1 Synthesis of leucine N-carboxyanhydride; 4.2.2 Synthesis of immobilized poly-D-leucine; 4.2.3 Asymmetric epoxidation of (E)-benzylideneacetophenone; 4.2.4 Conclusion; 4.3 Asymmetric epoxidation using chiral modified diethylzinc; 4.3.1 Epoxidation of 2-isobutylidene-1-tetralone; 4.3.2 Conclusion; 4.4 Asymmetric epoxidation of (E)-benzylideneacetophenone using the La-(R)-BINOL-Ph(3)PO/cumene hydroperoxide system; 4.4.1 Merits of the system; References; 5 Epoxidation of Allylic Alcohols 5.1 Non-asymmetric epoxidation5.2 Asymmetric epoxidation using a chiral titanium complex; 5.2.1 Epoxidation of cinnamyl alcohol; 5.2.2 Epoxidation of (E)-2-methyl-3-phenyl-2-propenol; 5.2.3 Epoxidation of (E)-2-hexen-1-ol; 5.2.4 Conclusion; 5.3 Asymmetric epoxidation of (E)-undec-2-en-1-ol using poly(octamethylene tartrate); 5.3.1 Synthesis of branched poly (octamethylene-L-(+)-tartrate); 5.3.2 Asymmetric epoxidation of (E)-undec-2-en-1-ol; References; 6 Epoxidation of Unfunctionalized Alkenes and a, b-Unsaturated Esters 6.1 Asymmetric epoxidation of disubstituted Z-alkenes using a chiral salen-manganese complex6.1.1 Epoxidation of (Z)-methyl styrene; 6.1.2 Epoxidation of (Z)-ethyl cinnamate; 6.1.3 Conclusion; 6.2 Asymmetric epoxidation of disubstituted E-alkanes using a D-fructose based catalyst; 6.2.1 Epoxidation of (E)-stilbene; 6.2.2 Conclusion; 6.3 Enantioselective epoxidation of (E)-b-methylstyrene by D(2)-symmetric chiral trans-dioxoruthenium (VI) porphyrins; 6.3.1 Preparation of the trans-dioxoruthenium(VI) complexes with D(2)-symmetric porphyrins (H(2)L(1-3)) 6.3.2 Enantioselective epoxidation of (E)-b-methylstyrene6.3.3 Conclusion; References; 7 Asymmetric Hydroxylation and Aminohydroxylation; 7.1 Asymmetric aminohydroxylation of 4-methoxystyrene; 7.1.1 Conclusion; 7.2 Asymmetric dihydroxylation of (1-cyclohexenyl)acetonitrile; 7.2.1 (R,R)-(1,2-Dihydroxycyclohexyl)acetonitrile acetonide; 7.2.2 Conclusion; References; 8 Asymmetric Sulfoxidation; 8.1 Asymmetric oxidation of sulfides and kinetic resolution of sulfoxides; 8.1.1 Asymmetric oxidation of 4-bromothioanisole; 8.1.2 Kinetic resolution of racemic 4-bromophenyl methyl sulfoxide; References 9 Asymmetric Reduction of Ketones Using Organometallic Catalysts |
| Record Nr. | UNISA-996218171503316 |
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Roberts Stanley M
|
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| Hoboken, : Wiley, 2003 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction
| Catalysts for fine chemical synthesis [[electronic resource] ] : hydrolysis, oxidation and reduction |
| Autore | Roberts Stanley M |
| Pubbl/distr/stampa | Hoboken, : Wiley, 2003 |
| Descrizione fisica | 1 online resource (245 p.) |
| Disciplina |
660.634
660/.28443 |
| Altri autori (Persone) | PoignantGeraldine |
| Collana | Catalysts For Fine Chemicals Synthesis |
| Soggetto topico |
Catalysts
Chemistry, Organic Enzymes Hydrolysis Organic compounds Oxidation-reduction reaction Synthesis Biomedical Engineering Health & Biological Sciences |
| ISBN |
1-280-27032-2
9786610270323 0-470-36296-0 0-470-85579-7 0-470-85580-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Catalysts for Fine Chemical Synthesis Volume 1; Contents; Series Preface; Preface to Volume 1; Abbreviations; PART I: REVIEW; 1 The Integration of Biotransformations into the Catalyst Portfolio; 1.1 Hydrolysis of esters, amides, nitriles and oxiranes; 1.2 Reduction reactions; 1.2.1 Reduction of carbonyl compounds; 1.2.2 Reduction of alkenes; 1.3 Oxidative transformations; 1.4 Carbon-carbon bond-forming reactions; 1.5 Conclusions; References; PART II: PROCEDURES; 2 General Information; 3 Asymmetric Epoxidation; 3.1 Introduction; References; 4 Epoxidation of a, b-Unsaturated Carbonyl Compounds
4.1 Non-asymmetric epoxidation4.2 Asymmetric epoxidation using poly-D-leucine; 4.2.1 Synthesis of leucine N-carboxyanhydride; 4.2.2 Synthesis of immobilized poly-D-leucine; 4.2.3 Asymmetric epoxidation of (E)-benzylideneacetophenone; 4.2.4 Conclusion; 4.3 Asymmetric epoxidation using chiral modified diethylzinc; 4.3.1 Epoxidation of 2-isobutylidene-1-tetralone; 4.3.2 Conclusion; 4.4 Asymmetric epoxidation of (E)-benzylideneacetophenone using the La-(R)-BINOL-Ph(3)PO/cumene hydroperoxide system; 4.4.1 Merits of the system; References; 5 Epoxidation of Allylic Alcohols 5.1 Non-asymmetric epoxidation5.2 Asymmetric epoxidation using a chiral titanium complex; 5.2.1 Epoxidation of cinnamyl alcohol; 5.2.2 Epoxidation of (E)-2-methyl-3-phenyl-2-propenol; 5.2.3 Epoxidation of (E)-2-hexen-1-ol; 5.2.4 Conclusion; 5.3 Asymmetric epoxidation of (E)-undec-2-en-1-ol using poly(octamethylene tartrate); 5.3.1 Synthesis of branched poly (octamethylene-L-(+)-tartrate); 5.3.2 Asymmetric epoxidation of (E)-undec-2-en-1-ol; References; 6 Epoxidation of Unfunctionalized Alkenes and a, b-Unsaturated Esters 6.1 Asymmetric epoxidation of disubstituted Z-alkenes using a chiral salen-manganese complex6.1.1 Epoxidation of (Z)-methyl styrene; 6.1.2 Epoxidation of (Z)-ethyl cinnamate; 6.1.3 Conclusion; 6.2 Asymmetric epoxidation of disubstituted E-alkanes using a D-fructose based catalyst; 6.2.1 Epoxidation of (E)-stilbene; 6.2.2 Conclusion; 6.3 Enantioselective epoxidation of (E)-b-methylstyrene by D(2)-symmetric chiral trans-dioxoruthenium (VI) porphyrins; 6.3.1 Preparation of the trans-dioxoruthenium(VI) complexes with D(2)-symmetric porphyrins (H(2)L(1-3)) 6.3.2 Enantioselective epoxidation of (E)-b-methylstyrene6.3.3 Conclusion; References; 7 Asymmetric Hydroxylation and Aminohydroxylation; 7.1 Asymmetric aminohydroxylation of 4-methoxystyrene; 7.1.1 Conclusion; 7.2 Asymmetric dihydroxylation of (1-cyclohexenyl)acetonitrile; 7.2.1 (R,R)-(1,2-Dihydroxycyclohexyl)acetonitrile acetonide; 7.2.2 Conclusion; References; 8 Asymmetric Sulfoxidation; 8.1 Asymmetric oxidation of sulfides and kinetic resolution of sulfoxides; 8.1.1 Asymmetric oxidation of 4-bromothioanisole; 8.1.2 Kinetic resolution of racemic 4-bromophenyl methyl sulfoxide; References 9 Asymmetric Reduction of Ketones Using Organometallic Catalysts |
| Record Nr. | UNINA-9910831084903321 |
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Roberts Stanley M
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| Hoboken, : Wiley, 2003 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Enzymatic saccharification of lignocellulosic biomass [[electronic resource] ] : laboratory analytical procedure (LAP) : issue date, 3/21/2008 / / M. Selig, N. Weiss, and Y. Ji
| Enzymatic saccharification of lignocellulosic biomass [[electronic resource] ] : laboratory analytical procedure (LAP) : issue date, 3/21/2008 / / M. Selig, N. Weiss, and Y. Ji |
| Autore | Selig M |
| Pubbl/distr/stampa | Golden, Colo. : , : National Renewable Energy Laboratory, , [2008] |
| Descrizione fisica | 5 pages : digital, PDF file |
| Altri autori (Persone) |
WeissN
JiY |
| Collana | Technical report |
| Soggetto topico |
Biomass conversion
Biomass Hydrolysis |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Enzymatic saccharification of lignocellulosic biomass |
| Record Nr. | UNINA-9910696520903321 |
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Selig M
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| Golden, Colo. : , : National Renewable Energy Laboratory, , [2008] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Estimation of hydrolysis rate constants of carboxylic acid ester and phosphate ester compounds in aqueous systems from molecular structure by SPARC [[electronic resource] /] / By S. H. Hilal
| Estimation of hydrolysis rate constants of carboxylic acid ester and phosphate ester compounds in aqueous systems from molecular structure by SPARC [[electronic resource] /] / By S. H. Hilal |
| Autore | Hilal S. H |
| Pubbl/distr/stampa | Washington, DC : , : U.S. Environmental Protection Agency, Office of Research and Development, , [2006] |
| Descrizione fisica | x, 102 pages : digital, PDF file |
| Soggetto topico |
Hydrolysis
Hydration |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Sparc Performs Automated Reasoning in Chemistry |
| Record Nr. | UNINA-9910696446503321 |
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Hilal S. H
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| Washington, DC : , : U.S. Environmental Protection Agency, Office of Research and Development, , [2006] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Ethanol production by enzymatic hydrolysis [[electronic resource] ] : parametric analysis of a base-case process / / Steven H. Isaacs
| Ethanol production by enzymatic hydrolysis [[electronic resource] ] : parametric analysis of a base-case process / / Steven H. Isaacs |
| Autore | Isaacs Steven H |
| Pubbl/distr/stampa | Golden, Colo. : , : Solar Energy Research Institute, , [1984] |
| Descrizione fisica | x, 64 pages : digital, PDF file |
| Soggetto topico |
Hydrolysis
Biomass conversion - Research Alcohol as fuel - Research |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Ethanol production by enzymatic hydrolysis |
| Record Nr. | UNINA-9910698322703321 |
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Isaacs Steven H
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| Golden, Colo. : , : Solar Energy Research Institute, , [1984] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Fibrinolysis & proteolysis
| Fibrinolysis & proteolysis |
| Pubbl/distr/stampa | New York, : Churchill Livingstone |
| Disciplina | 616 |
| Soggetto topico |
Fibrinolysis
Proteolysis Proteins - Metabolism Hydrolysis Proteins - metabolism |
| Soggetto genere / forma | Periodical |
| ISSN | 1532-222X |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti |
Fibrinolysis & proteolysis
Fibrinolysis and proteolysis |
| Record Nr. | UNISA-996209660303316 |
| New York, : Churchill Livingstone | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Fibrinolysis & proteolysis
| Fibrinolysis & proteolysis |
| Pubbl/distr/stampa | New York, : Churchill Livingstone |
| Disciplina | 616 |
| Soggetto topico |
Fibrinolysis
Thrombosis Proteins - Metabolism Hydrolysis Proteins - metabolism Fibrinolyse |
| Soggetto genere / forma |
Periodical
Periodicals. Ressource Internet (Descripteur de forme) Périodique électronique (Descripteur de forme) |
| ISSN | 1532-222X |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Fibrinolysis and proteolysis |
| Record Nr. | UNINA-9910333144203321 |
| New York, : Churchill Livingstone | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Soggetto topico
-
Hydrolysis
(25)
- Enzymes (7)
- Health & Biological Sciences (6)
- Hydration (4)
- Oxidation-reduction reaction (4)