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MARC Lista (tabellare)
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.  
[Golden, Colo.] : , : National Renewable Energy Laboratory, , [2021]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Opac: Controlla la disponibilità qui
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  
Hoboken, : Wiley, 2003
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Roberts Stanley M  
Hoboken, : Wiley, 2003
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
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
Roberts Stanley M  
Hoboken, : Wiley, 2003
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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-9910841318903321
Roberts Stanley M  
Hoboken, : Wiley, 2003
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Selig M  
Golden, Colo. : , : National Renewable Energy Laboratory, , [2008]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Hilal S. H  
Washington, DC : , : U.S. Environmental Protection Agency, Office of Research and Development, , [2006]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Isaacs Steven H  
Golden, Colo. : , : Solar Energy Research Institute, , [1984]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
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
Opac: Controlla la disponibilità qui