01410nam0 22003251i 450 UON0022993320231205103456.561IT887088126120030730d1985 |0itac50 baitaIT|||| |||||ˆIl ‰paragone della cavernavariazioni da Platone a oggiKonrad GaiserNapoliBibliopolis198597 p.22 cm.Fondo LucentiniIT-UONSI F.L.0247001UON001766712001 Memorie dell'Istituto Italiano per gli Studi Filosofici210 NapoliBibliopolis.13001UON003716902001 Variazioni da Platone a oggiPLATONISMOUONC020088FIPLATONEUONC049136FIITNapoliUONL000012184FILOSOFIA PLATONICA21GAISERKonradUONV077727151880BibliopolisUONV257071650ITSOL20240220RICAUON00229933SIBA - SISTEMA BIBLIOTECARIO DI ATENEOSI F.L. 0247 SI 12129 7 Fondo LucentiniBuonoSIBA - SISTEMA BIBLIOTECARIO DI ATENEOSI FS 01289 SI FP 6569 5 Paragone della caverna95483UNIOR05418nam 2200673 450 991081857400332120230807204754.01-118-96062-91-118-96055-61-118-96042-4(CKB)2670000000592465(EBL)1895815(SSID)ssj0001420882(PQKBManifestationID)11805037(PQKBTitleCode)TC0001420882(PQKBWorkID)11422675(PQKB)11204673(MiAaPQ)EBC1895815(DLC) 2014023772(Au-PeEL)EBL1895815(CaPaEBR)ebr11015198(CaONFJC)MIL719003(OCoLC)903956521(EXLCZ)99267000000059246520150212h20152015 uy 0engur|n|---|||||txtccrBiosynthesis of heterocycles from isolation to gene cluster /Patrizia Diana, Girolamo CirrincioneHoboken, New Jersey :Wiley,2015.©20151 online resource (783 p.)"A John Wiley & Sons, Inc., publication."1-322-87721-1 1-118-02867-8 Includes bibliographical references at the end of each chapters and index.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 Isotopes2.1.2 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 Cyclopenin3.2.10 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 Acids4.1.4 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 A5.1.7 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 Oroidin5.6.4 NikkomycinsThis book describes biosynthetic methods to synthesize heterocycliccompounds, offering a guide for the development of new drugs basedon natural products. The authors explain the role of naturalproducts in chemistry and their formation along with importantanalytical methods and techniques for working withheterocycles. Covers methods and techniques: isotopic labelling,enzymes and mutants, and pathway identification Provides a thorough resource of informationspecifically on heterocyclic natural products and their practicalbiosynthetic relevance Explains the role of natural products in chemistry aHeterocyclic compoundsSynthesisBiosynthesisHeterocyclic compoundsSynthesis.Biosynthesis.547/.59Diana Patrizia1642348Cirrincione GirolamoMiAaPQMiAaPQMiAaPQBOOK9910818574003321Biosynthesis of heterocycles3986980UNINA01199nam0 22002891i 450 UON0023323120231205103512.50020030730d1977 |0itac50 baitaIT|||| |||||ˆIl ‰ Corpus Dioysianum nel MedioevoRassegna di studi: 1900-1972Barbara Faes de MottoniBolognaIl Mulino1977247 p.21 cm.001UON001768442001 Pubblicazioni del centro di studio per la storia della storiografia filosofica210 BolognaIl Mulino.3Filosofia medievaleUONC019606FIPLATONISMOUONC020088FIITBolognaUONL000085189FILOSOFIA MEDIEVALE21FAES DE MOTTONIBarbaraUONV139581443823Il MulinoUONV245824650ITSOL20250606RICASIBA - SISTEMA BIBLIOTECARIO DI ATENEOUONSIUON00233231SIBA - SISTEMA BIBLIOTECARIO DI ATENEOSI FS 01369 SI LO 5443 5 Corpus Dioysianum nel Medioevo1233202UNIOR