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The alkaloids /
The Alkaloids, a series that has covered the topic for more than 60 years, is the leading book series in the field of alkaloid chemistry. In more than 70 volumes, all aspects of alkaloids-including their chemistry, biology, and pharmacology-are covered in high-quality, timeless reviews written by re...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Cambridge, MA :
Academic Press,
2017.
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| Temas: | |
| Acceso en línea: | Texto completo Texto completo |
MARC
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| 001 | SCIDIR_ocn973396829 | ||
| 003 | OCoLC | ||
| 005 | 20231120112214.0 | ||
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| 020 | |a 9780128111253 |q (electronic bk.) | ||
| 020 | |a 0128111259 |q (electronic bk.) | ||
| 020 | |z 9780128111246 | ||
| 020 | |z 0128111240 | ||
| 035 | |a (OCoLC)973396829 |z (OCoLC)974030545 |z (OCoLC)974318406 |z (OCoLC)974452161 | ||
| 050 | 4 | |a QD421 |b .A45 2017 | |
| 072 | 7 | |a SCI |x 007000 |2 bisacsh | |
| 082 | 0 | 4 | |a 572.549 |2 23 |
| 245 | 0 | 4 | |a The alkaloids / |c edited by Hans-Joachim Kn�olker. |
| 264 | 1 | |a Cambridge, MA : |b Academic Press, |c 2017. | |
| 300 | |a 1 online resource | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 588 | 0 | |a Online resource, title from PDF title page (EBSCO, viewed March 1, 2017). | |
| 520 | |a The Alkaloids, a series that has covered the topic for more than 60 years, is the leading book series in the field of alkaloid chemistry. In more than 70 volumes, all aspects of alkaloids-including their chemistry, biology, and pharmacology-are covered in high-quality, timeless reviews written by renowned experts in the field. | ||
| 505 | 0 | |a Front Cover; The Alkaloids Chemistry and Biology; The Alkaloids Chemistry and Biology; Contents; CONTRIBUTORS; PREFACE; One -- Acridone Alkaloids; 1. INTRODUCTION; 2. BIOSYNTHESIS; 3. OCCURRENCE AND CHARACTERIZATION; 3.1 Simple Acridone Alkaloids; 3.2 C-Prenyl Acridone Alkaloids; 3.3 Furoacridone Alkaloids; 3.4 Pyranoacridone Alkaloids; 3.5 Dimeric Acridone Alkaloids and Related Compounds; 3.6 Miscellaneous Alkaloids; 4. SYNTHESIS; 4.1 Simple Acridone Alkaloids; 4.1.1 Methods Involving the Cyclization of Diarylamine Intermediates | |
| 505 | 8 | |a 4.1.2 Methods Involving the Cyclization of Benzophenone Intermediates4.1.3 Other Methods; 4.2 C-Prenyl Acridone Alkaloids; 4.3 Furoacridone Alkaloids; 4.4 Pyranoacridone Alkaloids; 4.5 Azacridone-A; 4.6 Acrimarines; 5. BIOLOGICAL PROPERTIES; 5.1 Cytotoxicity and Anticancer Activity; 5.2 Antimicrobial Activity; 5.3 Antiparasitic Activity; 5.4 Enzyme Inhibition; 5.5 Other Biological Effects; 5.6 Biologically Active Synthetic Analogs of Acridone Alkaloids; ACKNOWLEDGMENTS; REFERENCES; Two -- Galbulimima Alkaloids; 1. INTRODUCTION; 2. ISOLATION AND CLASSIFICATION; 3. BIOLOGICAL PROPERTIES | |
| 505 | 8 | |a 4. BIOSYNTHESIS5. SYNTHESIS OF GALBULIMIMA ALKALOIDS; 5.1 Synthesis of Class I Galbulimima Alkaloids; 5.2 Synthesis of Class II Galbulimima Alkaloids; 5.3 Synthesis of Class III Galbulimima Alkaloids; 5.4 Synthesis of Class IV Galbulimima Alkaloids (Miscellaneous Alkaloids); 6. CONCLUSION; REFERENCES; Three -- Total Synthesis of Lundurine and Related Alkaloids: Synthetic Approaches and Strategies; 1. BACKGROUND; 2. SYNTHETIC APPROACHES; 2.1 Basic Strategies; 2.2 Synthesis of Azocine-Fused Indoles and Indolines; 2.3 Synthesis of Functionalized Cyclopropa[b]indole Core | |
| 505 | 8 | |a 3. TOTAL SYNTHESIS OF LUNDURINES A AND B BY NISHIDA4-63.1 First Synthesis of Lundurine B4; 3.1.1 Retrosynthetic Analysis of Lundurine B; 3.1.2 Model Study30; 3.1.3 Total Synthesis of (�)-Lundurine B4; 3.1.4 Unexpected Reactions Observed During Model Studies and Total Synthesis30; 3.2 Concise Synthesis of (�)-Lundurines A and B5; 3.3 Synthesis of ()-Lundurine B6; 4. SYNTHESIS OF ()-LUNDURINE A BY QIN9,10; 5. SYNTHESIS OF ()-LUNDURINES A-C BY ECHAVARREN11; 6. SYNTHESIS OF OTHER RELATED ALKALOIDS: (+)-LAPIDILECTINE B AND (+)-GRANDILODINE C54; 7. CONCLUSION; REFERENCES | |
| 505 | 8 | |a Four -- Cephalotaxus Alkaloids1. INTRODUCTION; 2. NATURAL OCCURRENCE, ISOLATION, AND STRUCTURAL ASSIGNMENT; 2.1 Cephalotaxine and Related Alkaloids; 2.2 Natural Cephalotaxus Esters; 2.3 Other Alkaloids; 2.4 Production and Purification Studies; 3. SYNTHESIS OF THE ALKALOID CORE; 3.1 Overview; 3.2 Racemic Syntheses; 3.2.1 C4-C13 Ring Closure a; 3.2.1.1 Tietze's Formal Synthesis (1997); 3.2.1.2 Suga and Yoshida's Formal Synthesis (2002, 2006); 3.2.1.3 Stoltz's Formal Synthesis (2007); 3.2.1.4 Huang's Formal Synthesis (2013); 3.2.1.5 Huang and Wang's Formal Synthesis (2015) | |
| 650 | 0 | |a Alkaloids. | |
| 650 | 2 | |a Alkaloids |0 (DNLM)D000470 | |
| 650 | 6 | |a Alcalo�ides. |0 (CaQQLa)201-0001052 | |
| 650 | 7 | |a SCIENCE |x Life Sciences |x Biochemistry. |2 bisacsh | |
| 650 | 7 | |a Alkaloids |2 fast |0 (OCoLC)fst00805398 | |
| 700 | 1 | |a Kn�olker, Hans-Joachim, |e editor. | |
| 776 | 0 | 8 | |i Print version: |z 0128111240 |z 9780128111246 |w (OCoLC)959872132 |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/10994831/77 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780128111246 |z Texto completo |