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Biosynthesis of heterocycles : from isolation to gene cluster / / Patrizia Diana, Girolamo Cirrincione
Biosynthesis of heterocycles : from isolation to gene cluster / / Patrizia Diana, Girolamo Cirrincione
Autore Diana Patrizia
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2015
Descrizione fisica 1 online resource (783 p.)
Disciplina 547/.59
Soggetto topico Heterocyclic compounds - Synthesis
Biosynthesis
ISBN 1-118-96062-9
1-118-96055-6
1-118-96042-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Contents; Preface; Acknowledgments; Chapter 1 Introduction; 1.1 Natural Products: Primary and Secondary Metabolites; 1.2 Common Reactions in Secondary Metabolites; 1.2.1 Alkylations; 1.2.2 Wagner-Meerwein Rearrangements; 1.2.3 Aldol and Claisen Reactions; 1.2.4 Schiff Base Formation and Mannich Reactions; 1.2.5 Transaminations; 1.2.6 Decarboxylations; 1.2.7 Oxidation and Reduction Reactions; 1.2.8 Dehalogenation/Halogenation Reactions; 1.2.9 Glycosylation Reactions; References; Chapter 2 Techniques for Biosynthesis; 2.1 Isotopic Labeling; 2.1.1 Stable Isotopes
2.1.2 Radioactive Isotopes2.2 Gene Coding for Enzymes; 2.3 Combinatorial Biosynthesis; References; Chapter 3 Three-Membered Heterocyclic Rings and Their Fused Derivatives; 3.1 Aziridines and Azirines; 3.1.1 Azicemicins; 3.1.2 Miraziridine; 3.1.3 Maduropeptin; 3.1.4 Azinomycins; 3.1.5 Ficellomycin; 3.1.6 Mitomycins; 3.1.7 Azirinomycin and Related Azirines; 3.2 Oxiranes and Oxirenes; 3.2.1 Fosfomycin; 3.2.2 AK, HC, and AF toxins; 3.2.3 Cerulenin; 3.2.4 Polyhydroxyalkanoates; 3.2.5 Epoxyrollins; 3.2.6 Asperlactone, Aspyrone, Asperline; 3.2.7 Tajixanthone; 3.2.8 Cyclomarin; 3.2.9 Cyclopenin
3.2.10 Ovalicin and Fumagillin3.2.11 Methylenomycin A; 3.2.12 Antibiotic LL-C10037; 3.2.13 Manumycins; 3.2.14 Scopolamine; 3.2.15 Iridoid Glucosides; 3.2.16 Cordiaquinone; 3.2.17 Cyclizidine and Indolizomycin; 3.2.18 Enediyne Antibiotics; 3.2.19 Macrolides; 3.2.20 Epothilones; 3.2.21 Pimaricin; 3.2.22 Hypothemycin; 3.2.23 Radicicol and Monocillin I; 3.2.24 Trichothecenes; 3.2.25 Sporolides A and B; References; Chapter 4 Four-Membered Heterocyclic Rings and Their Fused Derivatives; 4.1 Azetidine and Azetines; 4.1.1 Azetidine-2-carboxylic acid; 4.1.2 Polyoxins; 4.1.3 Mugineic Acids
4.1.4 Tabtoxin and Tabtoxinine-β-lactam4.1.5 Nocardicins; 4.1.6 Thienamycin; 4.1.7 Clavulanic Acid and Clavams; 4.1.8 Penicillins and Cephalosporins; 4.2 Oxetanes; 4.2.1 Oxetanocins; 4.2.2 Salinosporamides; 4.2.3 Taxol; 4.3 Dithiethanes; 4.3.1 Tropodithietic acid and Thiotropocin; References; Chapter 5 Five-Membered Heterocyclic Rings and Their Fused Derivatives; 5.1 Pyrroles (Including Tetrapyrroles); 5.1.1 2-Acetyl-1-pyrroline; 5.1.2 Pyrrolnitrin; 5.1.3 Broussonetines; 5.1.4 Prodigiosin and Undecylprodigiosin; 5.1.5 Anatoxin-a and Homoanatoxin-a; 5.1.6 Nostopeptolides A
5.1.7 Pyrrolizidine Alkaloids5.1.8 Toyocamycin and Sangivamycin; 5.1.9 Tetrapyrroles; 5.2 Indoles; 5.2.1 Indole-3-acetic acid and Glucobrassicin; 5.2.2 Camalexin; 5.2.3 Cyclomarazines; 5.2.4 Rebeccamycin and Staurosporine; 5.2.5 Paxilline; 5.3 Furans; 5.3.1 Furanomycin; 5.3.2 Xenofuranones A and B; 5.3.3 Acyl α- L-Rhamnopyranosides and Rhamnosyllactones; 5.3.4 Tuscolid and Tuscoron A and B; 5.3.5 Tetronomycin and Tetronasin; 5.3.6 Nonactin and Macrotetrolides; 5.3.7 Furanonaphthoquinone I; 5.4 Thiophenes; 5.5 Pyrazoles; 5.6 Imidazoles; 5.6.1 Histidine; 5.6.2 Amaranzole A; 5.6.3 Oroidin
5.6.4 Nikkomycins
Record Nr. UNINA-9910140487903321
Diana Patrizia  
Hoboken, New Jersey : , : Wiley, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Biosynthesis of heterocycles : from isolation to gene cluster / / Patrizia Diana, Girolamo Cirrincione
Biosynthesis of heterocycles : from isolation to gene cluster / / Patrizia Diana, Girolamo Cirrincione
Autore Diana Patrizia
Pubbl/distr/stampa Hoboken, New Jersey : , : Wiley, , 2015
Descrizione fisica 1 online resource (783 p.)
Disciplina 547/.59
Soggetto topico Heterocyclic compounds - Synthesis
Biosynthesis
ISBN 1-118-96062-9
1-118-96055-6
1-118-96042-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Contents; Preface; Acknowledgments; Chapter 1 Introduction; 1.1 Natural Products: Primary and Secondary Metabolites; 1.2 Common Reactions in Secondary Metabolites; 1.2.1 Alkylations; 1.2.2 Wagner-Meerwein Rearrangements; 1.2.3 Aldol and Claisen Reactions; 1.2.4 Schiff Base Formation and Mannich Reactions; 1.2.5 Transaminations; 1.2.6 Decarboxylations; 1.2.7 Oxidation and Reduction Reactions; 1.2.8 Dehalogenation/Halogenation Reactions; 1.2.9 Glycosylation Reactions; References; Chapter 2 Techniques for Biosynthesis; 2.1 Isotopic Labeling; 2.1.1 Stable Isotopes
2.1.2 Radioactive Isotopes2.2 Gene Coding for Enzymes; 2.3 Combinatorial Biosynthesis; References; Chapter 3 Three-Membered Heterocyclic Rings and Their Fused Derivatives; 3.1 Aziridines and Azirines; 3.1.1 Azicemicins; 3.1.2 Miraziridine; 3.1.3 Maduropeptin; 3.1.4 Azinomycins; 3.1.5 Ficellomycin; 3.1.6 Mitomycins; 3.1.7 Azirinomycin and Related Azirines; 3.2 Oxiranes and Oxirenes; 3.2.1 Fosfomycin; 3.2.2 AK, HC, and AF toxins; 3.2.3 Cerulenin; 3.2.4 Polyhydroxyalkanoates; 3.2.5 Epoxyrollins; 3.2.6 Asperlactone, Aspyrone, Asperline; 3.2.7 Tajixanthone; 3.2.8 Cyclomarin; 3.2.9 Cyclopenin
3.2.10 Ovalicin and Fumagillin3.2.11 Methylenomycin A; 3.2.12 Antibiotic LL-C10037; 3.2.13 Manumycins; 3.2.14 Scopolamine; 3.2.15 Iridoid Glucosides; 3.2.16 Cordiaquinone; 3.2.17 Cyclizidine and Indolizomycin; 3.2.18 Enediyne Antibiotics; 3.2.19 Macrolides; 3.2.20 Epothilones; 3.2.21 Pimaricin; 3.2.22 Hypothemycin; 3.2.23 Radicicol and Monocillin I; 3.2.24 Trichothecenes; 3.2.25 Sporolides A and B; References; Chapter 4 Four-Membered Heterocyclic Rings and Their Fused Derivatives; 4.1 Azetidine and Azetines; 4.1.1 Azetidine-2-carboxylic acid; 4.1.2 Polyoxins; 4.1.3 Mugineic Acids
4.1.4 Tabtoxin and Tabtoxinine-β-lactam4.1.5 Nocardicins; 4.1.6 Thienamycin; 4.1.7 Clavulanic Acid and Clavams; 4.1.8 Penicillins and Cephalosporins; 4.2 Oxetanes; 4.2.1 Oxetanocins; 4.2.2 Salinosporamides; 4.2.3 Taxol; 4.3 Dithiethanes; 4.3.1 Tropodithietic acid and Thiotropocin; References; Chapter 5 Five-Membered Heterocyclic Rings and Their Fused Derivatives; 5.1 Pyrroles (Including Tetrapyrroles); 5.1.1 2-Acetyl-1-pyrroline; 5.1.2 Pyrrolnitrin; 5.1.3 Broussonetines; 5.1.4 Prodigiosin and Undecylprodigiosin; 5.1.5 Anatoxin-a and Homoanatoxin-a; 5.1.6 Nostopeptolides A
5.1.7 Pyrrolizidine Alkaloids5.1.8 Toyocamycin and Sangivamycin; 5.1.9 Tetrapyrroles; 5.2 Indoles; 5.2.1 Indole-3-acetic acid and Glucobrassicin; 5.2.2 Camalexin; 5.2.3 Cyclomarazines; 5.2.4 Rebeccamycin and Staurosporine; 5.2.5 Paxilline; 5.3 Furans; 5.3.1 Furanomycin; 5.3.2 Xenofuranones A and B; 5.3.3 Acyl α- L-Rhamnopyranosides and Rhamnosyllactones; 5.3.4 Tuscolid and Tuscoron A and B; 5.3.5 Tetronomycin and Tetronasin; 5.3.6 Nonactin and Macrotetrolides; 5.3.7 Furanonaphthoquinone I; 5.4 Thiophenes; 5.5 Pyrazoles; 5.6 Imidazoles; 5.6.1 Histidine; 5.6.2 Amaranzole A; 5.6.3 Oroidin
5.6.4 Nikkomycins
Record Nr. UNINA-9910818574003321
Diana Patrizia  
Hoboken, New Jersey : , : Wiley, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui