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Stereoselective synthesis. Part H /
Studies in Natural Products Chemistry Volume 12: Stereoselective Synthesis (Part H) reviews the stereoselective synthetic and mechanistic chemistry of bicyclomycin. It discusses chemical studies of the taxane diterpenes; the synthetic methodology for 2-amino alcohols of biological interest; and the...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Amsterdam ; Oxford ; New York :
Elsevier,
1993.
|
| Colección: | Studies in natural products chemistry ;
12. |
| Temas: | |
| Acceso en línea: | Texto completo Texto completo |
MARC
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| 245 | 0 | 0 | |a Stereoselective synthesis. |n Part H / |c edited by Atta-ur-Rahman. |
| 264 | 1 | |a Amsterdam ; |a Oxford ; |a New York : |b Elsevier, |c 1993. | |
| 300 | |a 1 online resource (xii, 528 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Studies in natural products chemistry ; |v 12 | |
| 588 | 0 | |a Print version record. | |
| 504 | |6 880-01 |a References | ||
| 505 | 0 | |a Front Cover; Stereoselective Synthesis (Part H); Copyright Page; FOREWORD; PREFACE; Table of Contents ; CONTRIBUTORS; PART 1: Stereoselective Synthesis; Chapter 1. Synthetic Routes to the Oxahydrindene Subunit of the Avermectin- Milbemycin Family of Antiparasitic Agents: A Review; 1. Introduction: Isolation, Structure Elucidation, Biosynthesis, and Biological Activity of the Avermectins; 2. Synthetic Routes to the Oxahydrindene Subunit of the Avermectins; Acknowledgments.; References; Chapter 2. A New Tandem Process and its Application to the Synthesis of Macrolide Antibiotics | |
| 505 | 8 | |a 1. Introduction2. A new tandem process (Two-stage coupling process); 3. Synthesis of the rifamycin S ansa-chain compound; 4. Synthesis of the rifamycin W ansa-chain compound; 5. Total synthesis of rifamycin W; 6. Total synthesis of erythronolide A; 7. Total synthesis of erythromycin A; 8. Mechanistic considerations about the diastereoselective first step (Stage I) of the new tandem process; References; Chapter 3. Stereoselective Synthetic and Mechanistic Chemistry of Bicyclomycin; INTRODUCTION; ISOLATION, STRUCTURAL ELUCIDATION AND BIOSYNTHESIS; MECHANISM OF ACTION; CONCLUDING REMARKS | |
| 505 | 8 | |a 2. TOTAL SYNTHESIS3. THE DEVELOPMENT OF AN A-RING ANNULATION STRATEGY FOR TAXANE SYNTHESIS; 4. PARTIAL SYNTHESIS OF TAXOL AND ITS STRUCTURE-AOTVITY PROFILE; 5. BIOLOGICALLY ACTIVE TAXOL ANALOGUES WITH DELETED �A-RING SIDECHAIN SUBSTITUENTS AND VARIABLE C-2' CONFIGURATIONS; ACKNOWLEDGMENT.; REFERENCES; Chapter 7. Recent Advances in the synthesis of Tumor-Promoting Diterpenes; 1. INTRODUCTION; 2. INGENANE SYNTHETIC STUDIES; 3. PHORBOL SYNTHETIC STUDIES; REFERENCES; Chapter 8. Hydroxylated Indolizidines and their Synthesis; 1. Introduction; 2. The 1-hydroxyindolizidines (octahydroindolizin-l-ols) | |
| 505 | 8 | |a 3. The 2-hydroxyindoIizidines (octahydroindolizin-2-ols)4. The 5-hydroxy-4-oxyindolizidines; 5. The 6-hydroxyindolizidines (octahydroindo!izin-6-oIs); 6. The 7-hydroxyindoIizidines (octahydroindolizin-7-oIs); 7. Elaeokanine C; 8. The 8-hydroxyindoIizidines (octahydroindolizin-8-oIs); 9. The pumiliotoxins; 10. The allopumiliotoxins; 11. The 8a-hydroxyindoIizidines (octahydroindolizin-8a-oIs); 12. The 1,2-dihydroxyindoIizidines (octahydroindoIizin-l,2-dioIs); 13. Slaframine; 14. Swainsonine; 15. Swainsonine stereomers; 16. Castanospermine; 17. Castanospermine stereomers and analogues | |
| 520 | |a Studies in Natural Products Chemistry Volume 12: Stereoselective Synthesis (Part H) reviews the stereoselective synthetic and mechanistic chemistry of bicyclomycin. It discusses chemical studies of the taxane diterpenes; the synthetic methodology for 2-amino alcohols of biological interest; and the synthesis and structure of hydroxylated indolizidines. Some of the topics covered in the book are the synthetic routes to the oxahydrindene subunit of the avermectin-milbemycin family of antiparasitic agents; isolation, structure elucidation, biosynthesis, and biological activity of the avermectins | ||
| 650 | 0 | |a Natural products. | |
| 650 | 0 | |a Organic compounds |x Synthesis. | |
| 650 | 6 | |a Produits naturels. |0 (CaQQLa)201-0030192 | |
| 650 | 6 | |a Compos�es organiques |x Synth�ese. |0 (CaQQLa)201-0020323 | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Natural products |2 fast |0 (OCoLC)fst01034390 | |
| 650 | 7 | |a Organic compounds |x Synthesis |2 fast |0 (OCoLC)fst01047668 | |
| 700 | 1 | |a Rahman, Atta-ur-, |d 1942- | |
| 776 | 0 | 8 | |i Print version: |t Stereoselective synthesis. Part H. |z 0444893660 |w (OCoLC)28066248 |
| 830 | 0 | |a Studies in natural products chemistry ; |v 12. | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780444893666 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/15725995/12/part/PH |z Texto completo |
| 880 | |6 504-01/(S |a REFERENCES AND FOOTNOTESChapter 4. The Role of Isocyanides in the Synthesis of β-Lactam Antibiotics and Related Compounds; 1. INTRODUCTION; 2. �-LACTAM ANTIBIOTICS; 3. MODIFICATIONS OF β-LACTAM ANTIBIOTICS THROUGH ISOCYANIDE CHEMISTRY; 4. PERSPECTIVES; REFERENCES; Chapter 5. Synthesis of the lβ-Methylcarbapenem Key Intermediates Yoshio Ito and Shiro Terashima; 1. Introduction; 2. Construction of the Carbapenem Framework; 3. Synthesis of Key lβ-Methylcarbapenem Intermediates; References; Chapter 6. Chemical Studies of the Taxane Diterpenes Charles S. Swindell; 1. INTRODUCTION | ||