Fortschritte der Chemie organischer Naturstoffe

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Fortschritte der Chemie organischer Naturstoffe / herausgegeben von L. Zechmeister ... [et al.]

資料種別:

図書

出版情報:

Wien : Springer, 1938-

形態:

v. ; 24 cm

著者名:

ISBN:

9783211809754 [3211809759] (28 : Wien)
9783211810248 [3211810242] (29 : Wien)
9783211810620 [3211810625] (30 : Wien)
9783211811726 [3211811729] (31 : Wien)
9783211812556 [3211812555] (32 : Wien)
9783211813577 [3211813578] (33 : Wien)
9780387813578 [0387813578] (33 : NeW York)
9783211814154 [3211814159] (34 : Wien)
9780387814155 [0387814159] (34 : New York)
9783211814604 [3211814604] (35 : Wien)
9780387814605 [0387814604] (35 : New York)
9783211814727 [3211814728] (36 : Wien)
9780387814728 [0387814728] (36 : New York)
9783211815281 [3211815287] (37 : Wien)
9780387815282 [0387815287] (37 : New York)
9783211815298 [3211815295] (38 : Wien)
9780387815299 [0387815295] (38 : New York)
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9780387817415 [0387817417] (43 : New York)
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9783211819692 [321181969X] (50)
9783211819722 [321181972X] (51)
9783211819890 [3211819894] (52 : Wien)
9780387819891 [0387819894] (52 : New York)
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9780387825335 [0387825339] (64 : New York)
9783211825761 [3211825762] (65 : Wien)
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9783211830192 [3211830197] (73 : Wien)
9783211830338 [3211830332] (74 : Wien)
9783211830536 [3211830537] (75 : Wien)
9783211831656 [3211831657] (76 : Wien)
9783211832646 [3211832645] (77 : Wien)
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9783211834282 [3211834281] (80)
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9783211836019 [3211836012] (83)
9783211837078 [3211837078] (84)
9783211837832 [3211837833] (85)
9783211838891 [3211838899] (86)
9783211027806 [3211027807] (87)
9783211206881 [3211206884] (88)
9783211740187 [321174018X] (89)
9783211996607 [3211996605] (92)
9783709101391 [3709101395] (93)

書誌ID:

BA0096933X

子書誌情報

フルテキスト

所蔵情報

他の版・巻

書誌詳細

その他の標題:

Progress in the chemistry of organic natural products
Progrès dans la chimie des substances organiques naturelles

ISSN:

00717886

注記:

42:Authors, Y. Asakawa, M. Heidelberger
43:Authors, J. L. Ingham, A. Koskinen, M. Lounasmaa
52: Authors, H. Achenbach ... [et al.]
57: Authors, E. Casadevall ... [et al.]
59: Authors, A.-M. Eklund, S.-I. Hatanaka, I. Wahlberg
61: Authors, D.G.I. Kingston ... [et al.]
65: Author, Y. Asakawa
86: Author, A. Gossauer
87: Authors, H. Budzikiewicz ... [et al.]
88: Authors, J.F. Grove, E. Reimann, S. Roy
89: Authors, B. Kräutler ... [et al.]
90: The epothilones : an outstanding family of anti-tumor agents : from soil to the clinic / Authors, K.-H. Altmann ... [et al.]
91: Naturally occurring organohalogen compounds : a comprehensive update / Author: G. W. Gribble
92: Authors, H. Budzikiewicz ... [et al.]
93: Authors, S.A. Begum ... [et al.]
子書誌あり

主題:

天然物質の化学

言語:

英語

目次情報:

The Dolastatins / Robert D. ; G.R. Pettit ; T. Nomura ; Shashi B. Mahato ; D.C. Gournelis ; H. Murray

The Naturally Occurring Coumarins: Scope of the Review / T. Fukai ; Saraswati Garai ; G.G. Laskaris ; A. CavF

Phenolic Constituents of Licorice (Glycyrrhiza Species): Triterpenoid Saponins

Triterpenoid Saponins

Progress in the Past Three Years / R. Verpoorte

Phenolic Compounds / B. FigadTre

Introduction

Introduction to Tables

Recent Methods of Structure Determination of Prenylated Phenols

Isolation

Cyclopeptide Alkaloids

Biological Activities of Phenolic Constituents of Glycyrrhiza Species / A. LaurensSchemes and Tables：

Structure Elucidation

Biological Activity / L.A. CollettScheme 1：

Variations of Ring-Attached Five-Carbon Units found in Coumarins

Production of Saponins by Tissue Culture / D. Cortes

Future Possibilities / M.T. Davies-ColemanScheme 2：

Variations of Five-Carbon Units Attached to Carbon and Oxygen in Coumarins

Acetogenins from Annonaceae

Reports of New Triterpenoid Saponins

Non-Oxygenated Coumarins / D.E.A. Rivett ; Leena A. OtsomaaTable 1：

Naturally Occurring 6-Substituted 5,6-Dihydro-Alpha-Pyrones

Oxygenated Coumarins / Ari M.P. KoskinenTables 2-7：

Synthesis of 6-Deoxyamino Sugars / Tables 8-16：

Dioxygenated Coumarins

Introduction; Known 6-Deoxyaminohexoses

Synthetic aspects / Tables 17-28：

Trioxygenated Coumarins

Tetraoxygenated Coumarins / Tables 29-34：

Biscoumarins / Table 35：

Triscoumarins / Table 36：

Structure Revision Required / Table 37：

Non-Macrocyclic Trichothecenes, Part 2 / J.F. Grove

Cardiac GlycosidesD. Deepak / S. Srivastava ; N.K. Khare ; A. Khare

Aspects of the Enzymology of the Shikimate Pathway / E. Haslam

Naturally Occurring Isocyano/Isothiocyanato and Related Compounds / C. W. J. Chang

Monoterpene Indole Alkaloids from Blue-Green Algae

Marine Diterpenes from Sponges

Marine Sesquiterpenes from Sponges

Uncommon Marine Analogs

Other Terrestrial Compounds

Biogenesis and Biosynthesis

Discussion and Summary

Addendum

Acknowledgment

References

Sulfur-Containing Amides from Glycosmis Species (Rutaceae) / O. Hofer ; H. Greger

Isolation and Structure Elucidation

Methylthiopropenoic Acid Amides

Methylsulfinylpropenoic Acid Amides

Methylsulfonylpropenoic Acid Amides

Methylthiocarbonic Acid Amides

Synthesis of Biogenic Sulfur-Containing Amides

Biosynthesis

Chemotaxonomy

Appendix: Sulfur-Containing Bisamides from Aglaia Species (Meliaceae)

List of Contributors

Synthesis Pathways to Erythrina Alkaloids and Erythrina Type Compounds / E. Reimann

Structural Classification of Erythrina Alkaloids / 1：

New Erythrina Alkaloids / 3：

Biosynthesis of Erythrina Alkaloids / 4：

Erythrinane Alkaloids / 4.1：

Homoerythrinane Alkaloids / 4.2：

Syntheses of Erythrina Alkaloids and Erythrina Type Compounds / 5：

Methodical Classification / 5.1：

Erythrinanes / 5.2：

Final Formation of One Ring / 5.2.1：

Ring C (Route C) / 5.2.1.1：

Cyclization of N-Phenethylhydroindole Derivatives (Route C(a)) / 5.2.1.1.1：

Cyclization of Angulary Arylated Hydroindole Derivatives (Route C(b)) / 5.2.1.1.2：

Formation of Ring B (Route B) / 5.2.1.2：

Cyclization of N-substituted C5-Spiroisoquinoline Derivatives (Route B(a)) / 5.2.1.2.1：

Cyclization of C6-Substituted C5-Spiroisoquinoline Derivatives (Route B(b)) / 5.2.1.2.2：

Formation of Ring A (Route A) / 5.2.1.3：

Cycloaddition to Pyrroloisoquinolines (Route A(a)) / 5.2.1.3.1：

Intramolecular Aldol Condensation of Angularly Substituted Pyrroloisoquinoline (Route A(b)) / 5.2.1.3.2：

Simultaneous Formation of More Than One Ring / 5.2.2：

Simultaneous Formation of Rings B and C (Route B/C) / 5.2.2.1：

Cyclization of Secondary Diphenethyl- or (Cycloalkyl)ethyl-phenethylamine Derivatives(Route B/C(a)) / 5.2.2.1.1：

Cyclization of Tertiary Cyclohexyl-ethyl-phenethyl-amide Derivatives (Route B/C(b)) / 5.2.2.1.2：

Cyclization of N-Substituted 1-Acyldihydroisoquinolinium Derivatives (Route A/B) / 5.2.2.2：

Cyclization of a Highly Functionalized Homoveratrylimide (Route A/B/C) / 5.2.2.3：

Homoerythrinanes / 5.3：

Biomimetic Routes / 5.3.1：

Final C Ring Formation Starting from N-Substituted Phenylhydroindoles / 5.3.2：

A Ring Formation by [2 + 2] Photocycloaddition to Pyrrolobenzazepines / 5.3.3：

Simultaneous B Ring Formation/C Ring Expansion Starting from Spiro-2-tetralones / 5.3.4：

Pharmacology / 6：

Concluding Remarks / 7：

The Trichothecenes and Their Biosynthesis / J. F. Grove (f)

The Trichothecenes

Macrocyclic and Non-Macrocyclic Compounds / 2.1：

Trichothecene Relatives / 2.2：

Sources / 2.3：

Oxygenation Pattern / 2.4：

Simple Trichothecenes / 3.1：

Mevalonic Acid to Trichodiene / 3.1.1：

Trichodiene to 12,13-Epoxytrichothecene and Isotrichodermol / 3.1.2：

Further Oxygenation and Esterification of the Trichothecene Nucleus: Biosynthesis of Specific Metabolites / 3.1.3：

Trichothecolone / 3.1.3.1：

Vomitoxin and Derivatives / 3.1.3.2：

T-2 Toxin / 3.1.3.3：

Nivalenol and Derivatives / 3.1.3.4：

Trichothecene Biosynthetic Gene Clusters / 3.1.4：

Trichoverroids and Macrocyclic Trichothecenes / 3.2：

Melanin, Melanogenesis, and Vitiligo / S. Roy3.3：

Melanin

Chemistry of Melanin / 1.1：

Isolation and Analysis

Solubilization

Protein Content

Carboxylic and Phenolic Function

Chemical Degradation / 2.5：

Reductive Methods / 2.5.1：

Oxidative Methods / 2.5.2：

Pyrolytic Methods / 2.5.3：

Spectroscopic Studies / 2.6：

UV and IR Spectroscopy / 2.6.1：

NMR Spectroscopy / 2.6.2：

X-Ray Defraction Study / 2.6.3：

ESR Study / 2.6.4：

Structure of Melanin / 2.7：

Melanin as Homopolymer / 2.7.1：

Melanin as Poikilopolymer / 2.7.2：

Melanin as Bipolymer / 2.7.3：

Biophysical Model of Melanin Structure / 2.7.4：

Structure of Phaeomelanin / 2.7.5：

Synthesis of Melanin / 2.8：

Electrochemical Synthesis / 2.8.1：

Photochemical Synthesis / 2.8.2：

Characteristic Biophysicochemical Properties of Melanin

Interaction of Melanin with Light

Melanin in UV and Visible Light

Melanin in the Photoprotection of Skin

Melanin as Light Screen in Eyes

Melanin and Its Redox Function

Binding Complexation and Medicinal Aspects of Melanin

Use of Melanin for Defence / 3.4：

Melanogenesis

Melanogenesis in vivo

Melanocytes / 4.1.1：

The Characteristics of the Enzyme / 4.1.2：

Regulation of Melanogenesis / 4.1.3：

Physiological Factors / 4.1.3.1：

Organic Sulfur Compounds / 4.1.3.2：

Metal Ions and Other Chemicals / 4.1.3.3：

Vitamins / 4.1.3.4：

Hormones / 4.1.3.5：

Neural Influence / 4.1.3.6：

Malpighian Cells / 4.1.3.7：

UV Light / 4.1.3.8：

Melanogenesis in vitro

Enzymatic Melanin Synthesis / 4.2.1：

Rearrangement of Dopachrome / 4.2.1.1：

Polymerization of DHI / 4.2.1.2：

Non-Enzymatic Melanin Synthesis: Model Reaction / 4.2.2：

Udenfriend System: A Model for Mixed Function Oxidase / 4.2.2.1：

Melanin Formation Under Udenfriend Conditions / 4.2.2.2：

Vitiligo

Melanocytotoxicity: Antimelanocyte-Antibodies Formation

The Immune Hypothesis

The Neural Hypothesis

The Self-Destruction Hypothesis / 5.2.3：

The Composite Hypothesis / 5.2.4：

Chemotherapy of Vitiligo

Psoralens

Psoralen Action and UV Light

Psoralen Action on Melanogenesis

Abnormal Biochemical Parameters in Vitiligo / 5.4：

Status of Tryptophan in the Melanogenic System / 5.5：

A Composite Hypothesis on Vitiligo / 5.6：

Author Index

Subject Index

List of Contributor

Pyrroles from Vertebrates / 1.：

Pyrroles from Invertebrates / 3.：

Pyrroles from Insects / 3.1.：

Pyrroles from Ants / 3.1.1.：

Pyrroles from Beetles / 3.1.2.：

Pyrrole Pheromones from Butterflies / 3.1.3.：

Pyrroles from Sponges / 3.2.：

Pyrrole-2-Carboxylates from Sponges / 3.2.1.：

Pyrrole-2-Carboxamides from Sponges / 3.2.2.：

Pyrrole-2-Carboxamides of the Oroidin Type / 3.2.2.1.：

Cyclized Oroidin Metabolites / 3.2.2.2.：

Dimeric Oroidin Metabolites / 3.2.2.3.：

Alkyl Pyrroles from Sponges / 3.2.3.：

Aryl Pyrroles from Sponges / 3.2.4.：

Hydroxy Pyrroles from Sponges / 3.2.5.：

Tetramic Acid Derivatives from Sponges / 3.2.6.：

Pyrroles from Other Invertebrates / 3.3.：

Aryl Pyrroles / 3.3.1.：

Other Pyrrole Derivatives / 3.3.2.：

Pyrroles from Protozoa / 3.4.：

Pyrroles from Plants / 4.：

Dihydropyrrolizine Derivatives / 4.1.：

Pyrrole-2-Carboxylic Acid Derivatives from Plants / 4.2.：

Pyrrolinone Derivatives in Plants / 4.3.：

Pyrroles from Fungi / 5.：

Pyrroles from Basidiomycetes / 5.1.：

Pyrroles from Deuteromycetes / 5.2.：

Pyrroles from Myxomycetes / 5.3.：

Pyrrolinone Derivatives in Fungi / 5.4.：

Tetramic Acid Derivatives in Fungi / 5.5.：

Pyrroles from Bacteria / 6.：

Halogenated Monopyrroles from Bacteria / 6.1.：

Halogenated Benzylpyrroles / 6.1.1.：

Halogenated Benzoylpyrroles / 6.1.2.：

Halogenated [alpha]-Arylpyrroles / 6.1.3.：

Halogenated [beta]-Arylpyrroles / 6.1.4.：

Pyrrole-2-carboxylates from Bacteria / 6.2.：

Pyrrole-2-carboxamides from Bacteria / 6.3.：

The Distamycin Group / 6.3.1.：

Pyrrol-2-carbacyl Derivatives from Bacteria / 6.4.：

[alpha]-Pyridylpyrroles from Bacteria / 6.5.：

Other Monopyrrole Derivatives from Bacteria / 6.6.：

Prodigiosins / 6.7.：

Prodigiosins from Eubacteria / 6.7.1.：

Prodiginines from Actinomycetes / 6.7.2.：

Hydroxy Pyrroles from Bacteria / 6.8.：

Tetramic Acid Derivatives from Prokaryotes / 6.9.：

Derivatives of 3-Acetyltetramic Acid from Actinomycetes / 6.10.：

Synthetic Aspects of Iridoid Chemistry / H. Franzyk

Classification of Iridoids

Availability and Production of Iridoids

Semi-Synthetic Conversions Between Iridoids

Monoterpene Alkaloids Structurally Related to Iridoids

Syntheses from Iridoids; References

The Defensive Chemistry of Ants / S. Leclercq ; J. C. Braekman ; D. Daloze ; J. M. Pasteels

Introduction; Alkaloids

Nonalkaloidal Compounds

Naturally Occurring Plant Coumarins / R.D.H. Murray

Artemisinin: An Endoperoxidic Antimalarial from Artemisia annua L / H. Ziffer ; R.J. Highet ; D.L. Klayman

Marine Glycolipids / E. Fattorusso ; A. Mangoni

Brassinosteroids / G. Adam ; J. Schmidt ; B. Schneider

Natural Occurrence and Distribution

Structures

Isolation and Purification

Analysis of Brassinosteroids

Synthesis; Biosynthesis

Metabolism of Brassinosteroids

Physiological Action

Molecular Mode of Action

Conclusions

Chemistry of the Neem Tree (//Azadirachta indica//A. Juss.) / A. Akhila ; K. Rani

Introduction; Chemistry of Limonoids; C-Seco Meliacins; Other Compounds

Secondary Metabolites and the Control of Some Blue Stain and Decay Fungi / W. A. Ayer ; L. S. Trifonov

Introduction; Blue Stain Fungi

Decay Causing Fungi

The Black Gall Effect

Condensed Tannins / D. Ferreira ; E. V. Brandt ; J. Coetzee ; E. Malan

Introduction; Formation of the Interflavanyl Bond in Oligomeric Proanthocyanidins

Cleavage of the Interflavanyl Bond in Oligomeric Proanthocyanidins

Rearrangement of the Pyran Heterocycle of Oligomeric Proanthocyanidins

Conformational Analysis of Dimeric Proanthocyanidins

Conclusion

Constituents of //Lactarius// (Mushrooms) / W. M. Daniewski ; G. Vidari

Introduction; Sesquiterpenes Isolated from //Lactarius//; Introduction to Parts 6 and 7 - Velutinal Esters and Related Sesquiterpenes

Chemistry of Sesquiterpenes of //Lactarius//

Nitric Oxide: Physiological Roles, Biosynthesis and Medical Uses / D. R. Adams ; M. Brochwicz-Lewinski ; A. R. Butler

Discovery in the Vasculature

Platelet Aggregation

NO and the Immune System

NO and the Nervous System

S-Nitrosothiols

NO Activity in the Mammalian Eye

The NO Biosynthetic Pathway

Mechanism of the Nitric Oxide Synthase-Catalysed Reaction

Nitric Oxide Synthase Structure

Clinical Uses of NO and Its Inhibitors

Acknowledgements

Microbial Siderophores / Herbert Budzikiewicz

Peptide Siderophores

Pyoverdins and Related Siderophores from Pseudomonas Spp

Azomonas and Azotobacter Siderophores

Anachelin

Actinomycetal Metabolites

Bacterial Hydroxamate Siderophores

Fungal L-Ornithine-Based Hydroxamate Siderophores

Catecholate Siderophores

Lipopeptidic Siderophores

Pseudomonas mendocina Siderophores / 2.9：

Siderophores Based on Diamino- and Triaminoalkane Skeletons

Rhizobactin

Hydroxamic Acid Siderophores

Citrate Siderophores

Siderophores with Two Hydroxamic Acid Units

Siderophores with 2-Oxoglutaric Acid Units

Siderophores with Two Catecholate Units / 4.3：

Siderophores with Two Citric Acid Units / 4.4：

Legiobactin / 4.5：

Pyochelin and Related Structures

Miscellaneous Siderophores

Selected Syntheses / 8：

Anachelin H / 8.1：

Alterobactin / 8.2：

Parabactin / 8.3：

Nannochelin A / 8.4：

Pyochelin / 8.5：

Epilog / 9：

Appendix

Notes Added in Proof

Resin Glycosides from the Morning Glory Family / Rogelio Pereda-Miranda ; Daniel Rosas-RamÃrez ; Jhon CastaÃ±eda-GÃ³mez

Ethnobotanical Background and Discovery

Structural Diversity

Chemical Composition

Resin Glycosides

Isolation Techniques

Structure Elucidation of Resin Glycosides

Degradative Chemical Methods

Spectroscopic Methods

Crystallographic Methods

Molecular Modeling

Strategies for Synthesis

Tricolorin A / 6.1：

Ipomoeassin E / 6.2：

Woodrosin I / 6.3：

Significance

Traditional Medicine and Morning Glories / 7.1：

Biological Activities / 7.2：

Pharmacology and Toxicology / 7.3：

Chemical Ecology / 7.4：

Chlorophyll Catabolites / B. Krautler

Chlorophyll Catabolites from Vascular Plants

Green Chlorophyll Degradation Products in Vascular Plants

Chlorophyllide a and b from Chlorophylls by Loss of the Phytol Side Chain / 2.1.1：

Reductive Path from b- to a-Type Chlorophyll(ide)s / 2.1.2：

Pheophorbide a from Chlorophyllide a by Removal of the Magnesium Ion / 2.1.3：

13[superscript 2]-Carboxy-pyropheophorbide a from Hydrolysis and Pyropheophorbide a from Overall Loss of the Methoxycarbonyl Group from Pheophorbide a / 2.1.4：

Non-green Chlorophyll Degradation Products from Vascular Plants

Discovery and Structure Analysis of Fluorescent Chlorophyll Catabolites / 2.2.1：

Preparation of the Elusive Red Chlorophyll Catabolite by Partial Synthesis / 2.2.2：

An Enzyme-bound Red Chlorophyll Catabolite from Enzymatic Oxygenation of Pheophorbide a / 2.2.3：

Fluorescent Chlorophyll Catabolites from Enzymatic Reduction of the Red Chlorophyll Catabolite / 2.2.4：

Model Experiments for the Reduction of the Red Chlorophyll Catabolite to Fluorescent Chlorophyll Catabolites / 2.2.5：

Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.6：

A Non-enzymatic Tautomerization Achieves the "Final" Transformation of Fluorescent Chlorophyll Catabolites to Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.7：

Peripheral Functional Groups and Conjugations Found in Non-fluorescent Colourless Chlorophyll Catabolites / 2.2.8：

Evidence for Further Breakdown of the Non-fluorescent Colourless Chlorophyll Catabolites in Higher Plants / 2.2.9：

Chlorophyll Catabolites from the Green Alga Chlorella protothecoides

Chlorophyll Catabolites from Marine Organisms

Conclusions and Outlook

Steroidal Saponins / N. P. Sahu ; S. Banerjee ; N. B. Mondal ; D. Mandal

Conventional Methods

Spectrometry Coupled with Chemical Methods

Modern Spectrometric Methods

Mass Spectrometry / 3.3.1：

[superscript 1]H NMR Spectroscopy / 3.3.2：

[superscript 13]C NMR Spectroscopy / 3.3.2.2：

2D NMR Spectroscopy / 3.3.2.3：

Cytotoxic Activity Against Cancer Cell Lines

Antifungal Activity

Miscellaneous Effects

Biosynthesis of Steroidal Glycosides

Report of New Steroidal Saponins (1998-Mid-2006)

Acknowledgement

Non-conventional Lignans: Coumarinolignans, Flavonolignans, and Stilbenolignans / Sajeli A. Begum ; Mahendra Sahai ; Anil B. Ray

Coumarinolignans

Occurrence of Coumarinolignans

Classification of Coumarinolignans

Structure Elucidation of Coumarinolignans

Chemistry of Coumarinolignans

Biological Activity of Coumarinolignans

Biogenesis of Coumarinolignans

Flavonolignans

Occurrence of Flavonolignans

Features of Flavonolignans and Their Classification

Structure Elucidation of Flavonolignans

Chemistry of Flavonolignans

Biological Activity of Flavonolignans / 3.5：

Biogenesis of Flavonolignans / 3.6：

Stilbenolignans

Occurrence and Features of Stilbenolignans

Structure Elucidation and Synthesis of Stilbenolignans

Biological Activity of Stilbenolignans

Biogenesis of Stilbenolignans

Picrotoxanes / Edda GÃ¶ssinger

Tabular Overview of the Picrotoxanes

Occurrence

Systematic and Geographic Occurrence of Picrotoxane-Containing Plants

Parasitic Plants

Picrotoxanes Found in Animals and Animal Products

The Riddle of the Scattered Taxonomic Occurrence of Picrotoxanes

Isolation of Picrotoxanes

Examples of Recent Isolation Procedures

Structure Determination of Picrotoxanes

Main Picrotoxanes of the Menispermaceae

Main Picrotoxanes of the Coriariaceae

Picrotoxanes Isolated from Toxic Honey

Picrotoxanes of the Picrodendraceae

Picrotoxanes from Dendrobium Species

Total Syntheses of Picrotoxanes

Overview

Description of the Syntheses

Biosynthesis of Picrotoxanes

Investigations on the Biosynthesis of Dendrobines

Investigations on the Biosynthesis of Sesquiterpene Picrotoxanes

Physiological Activity of Picrotoxanes

Toxicity

Picrotoxanes as Therapeutics

Picrotoxanes as Epileptogenic Compounds

Picrotoxanes as Tools in Neurobiological Research

Abbreviations

Combinatorial and Synthetic Biosynthesis in Actinomycetes / Marta Luzhetska ; Johannes HÃ¤rle ; Andreas Bechthold

Combinatorial Biosynthesis and Synthetic Biosynthesis

Achievements in Combinatorial Biosynthesis

Challenges for Combinatorial Biosynthesis

Synthetic Biosynthesis

The Dolastatins / Robert D. ; G.R. Pettit ; T. Nomura ; Shashi B. Mahato ; D.C. Gournelis ; H. Murray

The Naturally Occurring Coumarins: Scope of the Review / T. Fukai ; Saraswati Garai ; G.G. Laskaris ; A. CavF

Phenolic Constituents of Licorice (Glycyrrhiza Species): Triterpenoid Saponins

Triterpenoid Saponins

Progress in the Past Three Years / R. Verpoorte

Phenolic Compounds / B. FigadTre

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類似資料:

1 雑誌 Fortschritte der Chemie organischer Naturstoffe Springer	7 図書 Fortschritte der physikalischen Chemie D. Steinkopff
2 図書 Progress in chromatography, 1938-1947 Zechmeister, L. (László), 1889- Chapman & Hall	8 電子ブック Organo-л-Verbindungen als Hilfsmittel in der organischen Chemie / Bach, H., Falbe, Jürgen., Biermann, M., Brune, H.-A., Cornils, B., Erker, G., Fell, B., Frohning, D., Habermehl, G., … Georg Thieme Verlag
3 図書 Steroids, terpenoids, sugars, and miscellaneous classes Budzikiewicz, Herbert, Djerassi, Carl, 1923-, Williams, Dudley H. Holden-Day	9 図書物質の単離と精製 : 天然生理活性物質を中心として大岳, 望(1926-) 東京大学出版会
4 図書 Ausgewählte moderne Trennverfahren zur Reinigung organischer Stoffe Greene, Edward F. (Edward Forbes), Röck, H., Jost, W. Dr. Dietrich Steinkopff Verlag	10 図書 Comprehensive natural products chemistry (: set ; v. 9) Barton, Derek, Sir, 1918-, 中西, 香爾(1925-), Meth-Cohn, Otto Elsevier
5 図書 Fortschritte der Chemie, Physik und physikalischen Chemie G. Borntraeger	11 図書 Special lectures presented at the 3rd International Symposium on the Chemistry of Natural Products, held in Kyoto, Japan, 12-18 April, 1964 IUPAC International Symposium on the Chemistry of Natural Products, International Union of Pure and Applied Chemistry. … Butterworths
6 雑誌 Fortschritte der physikalischen Chemie Dr. Dietrich Steinkopff	12 図書 Aliphatic and related natural product chemistry (v. 1 ; v. 2 ; v. 3) Gunstone, F. D., Baker, R.A. Royal Society of Chemistry