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Development of acid functional groups and lactones during the thermal degradation of wood and wood components [[electronic resource] /] / by David W. Rutherford, Robert L. Wershaw, and James B. Reeves III
| Development of acid functional groups and lactones during the thermal degradation of wood and wood components [[electronic resource] /] / by David W. Rutherford, Robert L. Wershaw, and James B. Reeves III |
| Autore | Rutherford David W |
| Edizione | [Version 1.0.] |
| Pubbl/distr/stampa | Reston, Va. : , : U.S. Geological Survey, , 2008 |
| Descrizione fisica | vi, 43 pages : digital, PDF file |
| Altri autori (Persone) |
WershawR. L
ReevesJames B |
| Collana | Scientific investigations report |
| Soggetto topico |
Wood - Deterioration
Charcoal Lactones Organic acids Fire |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910696550003321 |
Rutherford David W
|
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| Reston, Va. : , : U.S. Geological Survey, , 2008 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Macrocyclic lactones in antiparasitic therapy [[electronic resource] /] / edited by J. Vercruysse and R.S. Rew
| Macrocyclic lactones in antiparasitic therapy [[electronic resource] /] / edited by J. Vercruysse and R.S. Rew |
| Pubbl/distr/stampa | Oxon, UK ; ; New York, NY, : CABI Pub., c2002 |
| Descrizione fisica | 1 online resource (446 p.) |
| Disciplina | 616.9/6061 |
| Altri autori (Persone) |
VercruysseJ (Jozef)
RewRobert S |
| Soggetto topico |
Avermectins
Lactones Macrocyclic compounds Antiparasitic agents |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-83358-0
9786610833580 0-85199-840-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contributors; Preface; 1 Chemistry, Pharmacology and Safety of the Macrocyclic Lactones; 2 Pharmacokinetics of the Macrocyclic Lactones: Conventional Wisdom and New Paradigms; 3 Mode of Action of the Macrocyclic Lactones; 4 Ecological Impact of Macrocyclic Lactones on Dung Fauna; 5 Resistance Against Macrocyclic Lactones; 6 The Use of Macrocyclic Lactones to Control Parasites of Cattle; 7 The Use of Macrocyclic Lactones to Control Parasites of Sheep and Goats; 8 The Use of Macrocyclic Lactones to Control Parasites of Horses; 9 The Use of Macrocyclic Lactones to Control Parasites of Pigs
10 The Use of Macrocyclic Lactones in the Control and Prevention of Heartworm and Other Parasites in Dogs and Cats11 The Use of Macrocyclic Lactones to Control Parasites of Domesticated Wild Ruminants; 12 The Use of Macrocyclic Lactones to Control Parasites of Exotic Pets; 13 The Use of Macrocyclic Lactones to Control Parasites of Humans; 14 Macrocyclic Lactones as Antiparasitic Agents in the Future; Index |
| Record Nr. | UNINA-9910450465503321 |
| Oxon, UK ; ; New York, NY, : CABI Pub., c2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Macrocyclic lactones in antiparasitic therapy [[electronic resource] /] / edited by J. Vercruysse and R.S. Rew
| Macrocyclic lactones in antiparasitic therapy [[electronic resource] /] / edited by J. Vercruysse and R.S. Rew |
| Pubbl/distr/stampa | Oxon, UK ; ; New York, NY, : CABI Pub., c2002 |
| Descrizione fisica | 1 online resource (446 p.) |
| Disciplina | 616.9/6061 |
| Altri autori (Persone) |
VercruysseJ (Jozef)
RewRobert S |
| Soggetto topico |
Avermectins
Lactones Macrocyclic compounds Antiparasitic agents |
| ISBN |
1-280-83358-0
9786610833580 0-85199-840-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contributors; Preface; 1 Chemistry, Pharmacology and Safety of the Macrocyclic Lactones; 2 Pharmacokinetics of the Macrocyclic Lactones: Conventional Wisdom and New Paradigms; 3 Mode of Action of the Macrocyclic Lactones; 4 Ecological Impact of Macrocyclic Lactones on Dung Fauna; 5 Resistance Against Macrocyclic Lactones; 6 The Use of Macrocyclic Lactones to Control Parasites of Cattle; 7 The Use of Macrocyclic Lactones to Control Parasites of Sheep and Goats; 8 The Use of Macrocyclic Lactones to Control Parasites of Horses; 9 The Use of Macrocyclic Lactones to Control Parasites of Pigs
10 The Use of Macrocyclic Lactones in the Control and Prevention of Heartworm and Other Parasites in Dogs and Cats11 The Use of Macrocyclic Lactones to Control Parasites of Domesticated Wild Ruminants; 12 The Use of Macrocyclic Lactones to Control Parasites of Exotic Pets; 13 The Use of Macrocyclic Lactones to Control Parasites of Humans; 14 Macrocyclic Lactones as Antiparasitic Agents in the Future; Index |
| Record Nr. | UNINA-9910784123203321 |
| Oxon, UK ; ; New York, NY, : CABI Pub., c2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Macrocyclic lactones in antiparasitic therapy / / edited by J. Vercruysse and R.S. Rew
| Macrocyclic lactones in antiparasitic therapy / / edited by J. Vercruysse and R.S. Rew |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Oxon, UK ; ; New York, NY, : CABI Pub., c2002 |
| Descrizione fisica | 1 online resource (446 p.) |
| Disciplina | 616.9/6061 |
| Altri autori (Persone) |
VercruysseJ (Jozef)
RewRobert S |
| Soggetto topico |
Avermectins
Lactones Macrocyclic compounds Antiparasitic agents |
| ISBN |
1-280-83358-0
9786610833580 0-85199-840-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contributors; Preface; 1 Chemistry, Pharmacology and Safety of the Macrocyclic Lactones; 2 Pharmacokinetics of the Macrocyclic Lactones: Conventional Wisdom and New Paradigms; 3 Mode of Action of the Macrocyclic Lactones; 4 Ecological Impact of Macrocyclic Lactones on Dung Fauna; 5 Resistance Against Macrocyclic Lactones; 6 The Use of Macrocyclic Lactones to Control Parasites of Cattle; 7 The Use of Macrocyclic Lactones to Control Parasites of Sheep and Goats; 8 The Use of Macrocyclic Lactones to Control Parasites of Horses; 9 The Use of Macrocyclic Lactones to Control Parasites of Pigs
10 The Use of Macrocyclic Lactones in the Control and Prevention of Heartworm and Other Parasites in Dogs and Cats11 The Use of Macrocyclic Lactones to Control Parasites of Domesticated Wild Ruminants; 12 The Use of Macrocyclic Lactones to Control Parasites of Exotic Pets; 13 The Use of Macrocyclic Lactones to Control Parasites of Humans; 14 Macrocyclic Lactones as Antiparasitic Agents in the Future; Index |
| Record Nr. | UNINA-9910809735003321 |
| Oxon, UK ; ; New York, NY, : CABI Pub., c2002 | ||
| 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-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 | ||
| ||
Soggetto topico
-
Lactones
(6)
- Antiparasitic agents (3)
- Avermectins (3)
- Macrocyclic compounds (3)
- Lactams (2)