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SCIDIR_ocn936322542 |
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OCoLC |
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20231120112049.0 |
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m o d |
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cr cnu---unuuu |
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160201s2016 ne ob 001 0 eng d |
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|a N$T
|b eng
|e rda
|e pn
|c N$T
|d IDEBK
|d YDXCP
|d EBLCP
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|d OPELS
|d OCLCF
|d OCLCQ
|d D6H
|d UKBTH
|d OCLCQ
|d OCLCO
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| 020 |
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|a 9780128048351
|q electronic bk.
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|a 0128048352
|q electronic bk.
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|z 9780128046821
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|a (OCoLC)936322542
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|a QD421
|b .A45 2016
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| 072 |
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|a SCI
|x 007000
|2 bisacsh
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|a 572/.549
|2 23
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| 245 |
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|a The alkaloids :
|b chemistry and biology.
|n Volume 76 /
|c edited by Hans-Joachim Kn�olker.
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| 250 |
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|a First edition.
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| 264 |
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1 |
|a Amsterdam :
|b Elsevier,
|c 2016.
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| 300 |
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|a 1 online resource
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| 336 |
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|a text
|b txt
|2 rdacontent
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| 337 |
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|a computer
|b c
|2 rdamedia
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| 338 |
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|a online resource
|b cr
|2 rdacarrier
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|a Online resource; title from PDF title page (EBSCO, viewed February 9, 2016)
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|a Includes bibliographical references and indexes.
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|a Front Cover; The Alkaloids Chemistry and Biology; Copyright; DEDICATION; Contents; CONTRIBUTORS; PREFACE; One -- Sarpagan-Ajmalan-Type Indoles: Biosynthesis, Structural Biology, and Chemo-Enzymatic Significance; 1. INTRODUCTION; 2. RAUVOLFIA ALKALOIDS-SOURCES, THERAPEUTIC VALUE, AND ENZYME DETECTION; 2.1 Choosing an Efficient Biological System; 2.2 The Alkaloid Pattern of Rauvolfia Cell Cultures; 2.3 Chemical Syntheses of Biosynthetic Intermediates; 2.4 Detection of Enzyme Activities and Enzyme Purification; 3. ENZYMES OF THE AJMALINE PATHWAY (AP); 3.1 Strictosidine Synthase (STR)
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| 505 |
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|a 4.3.2 Raucaffricine Glucosidase (RG)4.3.3 Perakine Reductase (PR); 4.4 Side Routes Beyond Perakine and Raucaffrinoline; 4.5 The Route Beyond Ajmaline; 4.5.1 Side Route: From Ajmaline to Raumaclines; 4.5.2 Biosynthesis of Raumaclines; 4.5.3 Dialdehyde Reductase; 5. MONITORING BIOCONVERSIONS BY IN VIVO NMR; 6. CHEMO-ENZYMATIC APPROACHES; 6.1 From Single to Bunch-From Strictosidine Synthase (STR) to Novel Alkaloids; 6.2 Chemo-Enzymatic Application of Raucaffricine Glucosidase (RG); 7. SUMMARY; ACKNOWLEDGMENTS; REFERENCES; Two -- Sarpagine and Related Alkaloids; 1. INTRODUCTION; 1.1 Classification
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|a 1.2 Biosynthesis2. OCCURRENCE; 2.1 Recently Isolated Sarpagine-Related Indole Alkaloids; 3. SPECTROSCOPY; 3.1 1H NMR Spectroscopy; 3.2 13C NMR Spectroscopy; 4. PHARMACOLOGY; 5. SYNTHESIS; 5.1 The Asymmetric Pictet-Spengler Reaction; 5.2 Synthesis of Sarpagine/Macroline-Related Indole Alkaloids; 5.2.1 The Enantiospecific Total Synthesis of (+)-Vellosimine (161) by Wang; 5.2.2 A Biomimetic Total Synthesis of (+)-Na-Methylvellosimine (168) by Martin et al.; 5.2.3 Synthesis of (+)-Na-Methyl-16-Epi-Pericyclivine (180)
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|a Alkaloids.
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|a Alcalo�ides.
|0 (CaQQLa)201-0001052
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| 650 |
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|a SCIENCE / Life Sciences / Biochemistry
|2 bisacsh
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| 650 |
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7 |
|a Alkaloids
|2 fast
|0 (OCoLC)fst00805398
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| 700 |
1 |
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|a Kn�olker, Hans-Joachim,
|e editor.
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| 856 |
4 |
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|u https://sciencedirect.uam.elogim.com/science/book/9780128046821
|z Texto completo
|
