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Natural lactones and lactams : synthesis, occurrence and biological activity / / edited by Tomasz Janecki
| Natural lactones and lactams : synthesis, occurrence and biological activity / / edited by Tomasz Janecki |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] |
| Descrizione fisica | 1 online resource (394 p.) |
| Disciplina | 547.59 |
| Altri autori (Persone) | JaneckiTomasz |
| Soggetto topico |
Lactones
Lactams |
| ISBN |
3-527-66693-1
3-527-66691-5 3-527-66694-X |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Natural Lactones and Lactams; Title Page; Copyright; Contents; Preface; List of Contributors; Chapter 1 Tetronic Acids; 1.1 Introduction; 1.2 Natural Occurrence, Biological Activities, and Biosynthesis; 1.3 5-Ylidene Tetronic Natural Products; 1.3.1 Pulvinic Acids and Pulvinones; 1.3.2 Agglomerins; 1.3.3 Tetronomycin; 1.3.4 Stemofoline Alkaloids; 1.3.5 Variabilin; 1.3.6 Tetrodecamycin; 1.4 5-Monosubstituted Tetronic Natural Products; 1.4.1 Carlic, Carlosic, Carolic, Carolinic, and Viridicatic Acids; 1.4.2 RK-682; 1.4.3 Massarilactone B; 1.4.4 Annularins F, G, and H; 1.4.5 Palinurin
1.4.6 Pesthetoxin1.4.7 Rotundifolides A and B; 1.5 5-Disubstituted Tetronic Natural Products; 1.5.1 5-Dialkyl Tetronic Natural Products; 1.5.1.1 Vertinolide; 1.5.1.2 Papyracillic Acid B; 1.5.1.3 Bisorbibutenolide; 1.5.2 5-Spirotetronic Natural Products; 1.5.2.1 Spirotetronic Antibiotics; 1.5.2.2 Ircinianin and Wistarin; 1.5.2.3 Stemonamine Alkaloids; 1.5.2.4 Abyssomicins; 1.6 5-Unsubstituted Tetronic Natural Products; 1.6.1 Tetronasin; 1.7 Conclusions; References; Chapter 2 Recent Advances in the Field of Naturally Occurring 5,6-Dihydropyran-2-ones; 2.1 Introduction 2.2 Synthetic Methodologies for 5,6-Dihydropyran-2-ones2.2.1 Lactonization of Substituted δ-Hydroxy Acid Derivatives; 2.2.2 Oxidation of Substituted Dihydropyran Derivatives; 2.2.3 Ring-Closing Metathesis; 2.2.4 Miscellaneous Methods; 2.3 Formation of Stereogenic Centers inside the Dihydropyrone Ring; 2.3.1 Use of Chiral Precursors; 2.3.1.1 Carbohydrate and Related Precursors; 2.3.1.2 Chiral Hydroxy Acids; 2.3.1.3 Chiral Epoxides; 2.3.1.4 Other Chirons; 2.3.2 Asymmetric (Enantioselective) Reactions; 2.3.2.1 Asymmetric (Enantioselective) Sharpless Epoxidations or Dihydroxylations 2.3.2.2 Asymmetric Aldol-Type Reactions2.3.2.3 Asymmetric Allylations; 2.3.2.4 Asymmetric Carbonyl Reductions; 2.3.2.5 Asymmetric Alkylations; 2.3.2.6 Asymmetric Epoxide Hydrolysis; 2.3.2.7 Asymmetric Cycloadditions; 2.3.2.8 Other Asymmetric Methods; 2.4 Pharmacological Properties of Pyrones; 2.5 Biosynthetic Formation of Pyrones; 2.6 Syntheses of Natural 5,6-Dihydropyran-2-ones Reported during the Period from 2006 to the First Half of 2012; References; Chapter 3 β-Lactams; 3.1 Introduction; 3.1.1 Biosynthesis of Penicillin and Cephalosporin; 3.2 Monocyclic β-Lactams 3.2.1 Biosynthesis of Nocardicin A3.2.2 Synthetic Approaches to Construct β-Lactam Ring; 3.2.2.1 Cycloaddition Reactions; 3.2.2.2 Cyclization Reactions; 3.2.2.3 Miscellaneous Approaches; 3.2.3 Biological Activity of Monocyclic 2-Azetidinones; 3.3 Penams; 3.3.1 Synthetic Approaches to Penam Skeleton; 3.3.2 Biological Activity of Penams; 3.4 Cephalosporins; 3.4.1 Synthetic Approaches to Cephalosporin Skeleton; 3.4.2 Biological Activity of Cephalosporins; 3.5 Clavulanic Acid; 3.5.1 Synthetic Approaches to Clavam Skeleton; 3.5.2 Biological Activity of Clavams; 3.6 Carbapenems 3.6.1 Synthetic Approaches to Carbapenem Skeleton |
| Record Nr. | UNINA-9910139021003321 |
| Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Natural lactones and lactams : synthesis, occurrence and biological activity / / edited by Tomasz Janecki
| Natural lactones and lactams : synthesis, occurrence and biological activity / / edited by Tomasz Janecki |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] |
| Descrizione fisica | 1 online resource (394 p.) |
| Disciplina | 547.59 |
| Altri autori (Persone) | JaneckiTomasz |
| Soggetto topico |
Lactones
Lactams |
| ISBN |
3-527-66693-1
3-527-66691-5 3-527-66694-X |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Natural Lactones and Lactams; Title Page; Copyright; Contents; Preface; List of Contributors; Chapter 1 Tetronic Acids; 1.1 Introduction; 1.2 Natural Occurrence, Biological Activities, and Biosynthesis; 1.3 5-Ylidene Tetronic Natural Products; 1.3.1 Pulvinic Acids and Pulvinones; 1.3.2 Agglomerins; 1.3.3 Tetronomycin; 1.3.4 Stemofoline Alkaloids; 1.3.5 Variabilin; 1.3.6 Tetrodecamycin; 1.4 5-Monosubstituted Tetronic Natural Products; 1.4.1 Carlic, Carlosic, Carolic, Carolinic, and Viridicatic Acids; 1.4.2 RK-682; 1.4.3 Massarilactone B; 1.4.4 Annularins F, G, and H; 1.4.5 Palinurin
1.4.6 Pesthetoxin1.4.7 Rotundifolides A and B; 1.5 5-Disubstituted Tetronic Natural Products; 1.5.1 5-Dialkyl Tetronic Natural Products; 1.5.1.1 Vertinolide; 1.5.1.2 Papyracillic Acid B; 1.5.1.3 Bisorbibutenolide; 1.5.2 5-Spirotetronic Natural Products; 1.5.2.1 Spirotetronic Antibiotics; 1.5.2.2 Ircinianin and Wistarin; 1.5.2.3 Stemonamine Alkaloids; 1.5.2.4 Abyssomicins; 1.6 5-Unsubstituted Tetronic Natural Products; 1.6.1 Tetronasin; 1.7 Conclusions; References; Chapter 2 Recent Advances in the Field of Naturally Occurring 5,6-Dihydropyran-2-ones; 2.1 Introduction 2.2 Synthetic Methodologies for 5,6-Dihydropyran-2-ones2.2.1 Lactonization of Substituted δ-Hydroxy Acid Derivatives; 2.2.2 Oxidation of Substituted Dihydropyran Derivatives; 2.2.3 Ring-Closing Metathesis; 2.2.4 Miscellaneous Methods; 2.3 Formation of Stereogenic Centers inside the Dihydropyrone Ring; 2.3.1 Use of Chiral Precursors; 2.3.1.1 Carbohydrate and Related Precursors; 2.3.1.2 Chiral Hydroxy Acids; 2.3.1.3 Chiral Epoxides; 2.3.1.4 Other Chirons; 2.3.2 Asymmetric (Enantioselective) Reactions; 2.3.2.1 Asymmetric (Enantioselective) Sharpless Epoxidations or Dihydroxylations 2.3.2.2 Asymmetric Aldol-Type Reactions2.3.2.3 Asymmetric Allylations; 2.3.2.4 Asymmetric Carbonyl Reductions; 2.3.2.5 Asymmetric Alkylations; 2.3.2.6 Asymmetric Epoxide Hydrolysis; 2.3.2.7 Asymmetric Cycloadditions; 2.3.2.8 Other Asymmetric Methods; 2.4 Pharmacological Properties of Pyrones; 2.5 Biosynthetic Formation of Pyrones; 2.6 Syntheses of Natural 5,6-Dihydropyran-2-ones Reported during the Period from 2006 to the First Half of 2012; References; Chapter 3 β-Lactams; 3.1 Introduction; 3.1.1 Biosynthesis of Penicillin and Cephalosporin; 3.2 Monocyclic β-Lactams 3.2.1 Biosynthesis of Nocardicin A3.2.2 Synthetic Approaches to Construct β-Lactam Ring; 3.2.2.1 Cycloaddition Reactions; 3.2.2.2 Cyclization Reactions; 3.2.2.3 Miscellaneous Approaches; 3.2.3 Biological Activity of Monocyclic 2-Azetidinones; 3.3 Penams; 3.3.1 Synthetic Approaches to Penam Skeleton; 3.3.2 Biological Activity of Penams; 3.4 Cephalosporins; 3.4.1 Synthetic Approaches to Cephalosporin Skeleton; 3.4.2 Biological Activity of Cephalosporins; 3.5 Clavulanic Acid; 3.5.1 Synthetic Approaches to Clavam Skeleton; 3.5.2 Biological Activity of Clavams; 3.6 Carbapenems 3.6.1 Synthetic Approaches to Carbapenem Skeleton |
| Record Nr. | UNINA-9910821663403321 |
| Weinheim, Germany : , : Wiley-VCH Verlag GmbH & Co. KGaA, , [2014] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Toxicological Evaluation of Certain Veterinary Drug Residues in Food : WHO Food Additives Series No 49
| Toxicological Evaluation of Certain Veterinary Drug Residues in Food : WHO Food Additives Series No 49 |
| Autore | (JECFA) Fifty-eighth meeting of the Joint FAO/ WHO Expert Committee on Food Additives |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | World Health Organization, 2002 |
| Descrizione fisica | 1 online resource (93 p.) |
| Disciplina | 363.192 |
| Soggetto topico |
Feed additive residues -- Analysis -- Congresses
Feed additive residues -- Toxicology -- Congresses Food contamination -- Analysis -- Congresses Veterinary drug residues -- Analysis -- Congresses Veterinary drug residues -- Toxicology -- Congresses Antiparasitic Agents Body Burden Pharmaceutical Preparations Food Safety Cefotaxime Environmental Pollution Evaluation Studies as Topic Cephacetrile Investigative Techniques Public Health Anti-Infective Agents Chemicals and Drugs Therapeutic Uses Analytical, Diagnostic and Therapeutic Techniques and Equipment Cephalosporins Environment and Public Health Delivery of Health Care beta-Lactams Pharmacologic Actions Thiazines Lactams Sulfur Compounds Azabicyclo Compounds Chemical Actions and Uses Organic Chemicals Bridged Bicyclo Compounds, Heterocyclic Amides Bridged Bicyclo Compounds Bridged-Ring Compounds Polycyclic Compounds Cefuroxime Food Contamination - analysis Drug Evaluation - veterinary Anthelmintics - toxicity Cefuroxime - toxicity Drug Residues - toxicity Veterinary Drugs - toxicity |
| ISBN |
9789240681439
9240681434 9780585474915 0585474915 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | ""Contents""; ""Preface""; ""Anthelmintic agents""; ""Doramectin""; ""Tiabenzadole (thiabenzadole)""; ""Antimicrobial agents""; ""Cefuroxime""; ""Annexes""; ""Annex 1 Reports and other documents resulting from previous meetings of the Joint FAO/WHO Expert Committee on Food Additives""; ""Annex 2 Abbreviations used in the monographs""; ""Annex 3 Participants in the fifty-sixth meeting of the Joint FAO/WHO Expert Committee on Food Additives""; ""Annex 4 Recommendations on compounds on the agenda and further toxicological studies and information required"" |
| Record Nr. | UNINA-9910143536603321 |
(JECFA) Fifty-eighth meeting of the Joint FAO/ WHO Expert Committee on Food Additives
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| World Health Organization, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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