The alkaloids. Volume 77 /

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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Άλλοι συγγραφείς: Knölker, Hans-Joachim (Επιμελητής έκδοσης)
Μορφή: Ηλ. βιβλίο
Γλώσσα:English
Έκδοση: Cambridge, MA : Academic Press, 2017.
Θέματα:
Διαθέσιμο Online:Full Text via HEAL-Link
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245 0 4 |a The alkaloids.  |n Volume 77 /  |c edited by Hans-Joachim Knölker. 
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 (<U+0012>)-Lundurine B6; 4. SYNTHESIS OF (<U+0012>)-LUNDURINE A BY QIN9,10; 5. SYNTHESIS OF (<U+0012>)-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. 
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700 1 |a Knölker, Hans-Joachim,  |e editor. 
776 0 8 |i Print version:  |z 0128111240  |z 9780128111246  |w (OCoLC)959872132 
856 4 0 |u https://www.sciencedirect.com/science/bookseries/10994831/77  |z Full Text via HEAL-Link