The Indole Alkaloids: The Simple Bases
J. E. Saxton
in R.H.F. Manske's "The Alkaloids", Vol. 8, Ch. 1, p 1-25 (1965) (https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.tryptamines.pdf)
(https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.tryptamines.pdf)
Contents
I. Introduction
II. Abrine and Hypaphorine
III. Gramine and Its Derivatives
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Gramine, 3-Aminomethylindole, and 3-Methylaminomethylindole
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. Donaxarine
IV. Tryptamine and Its Derivatives
V. Psilocin and Psilocybin
VI. 5-Hydroxytryptamine and Its Derivatives
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. 5-Hydroxytryptamine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. 5-Methoxy-N-methyltryptamine and 5-Methoxy-N,N-dimethyltryptamine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)C. Bufotenine
VII. Cryptolepine
References
____ ___ __ _
The Indole Alkaloids: Ergot Alkaloids
Arthur Stoll & Albert Hofmann
in R.H.F. Manske's "The Alkaloids", Vol. 8, Ch. 21, p 725-783 (1965) (https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.ergot.pdf)
(https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.ergot.pdf)
Contents
I. The Biology of Ergot and a Short History of Its Active Principles Up to the Discovery of Ergotamine
II. Structural Types with Tables of the Natural Ergot Alkaloids
III. Lysergic Acid and Isolysergic Acid
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Elucidation of Structure
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. Stereochemistry of Lysergic Acid and the Dihydrolysergic Acids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)C. Syntheses in the Dihydrolysergic Acid Series
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)D. Synthesis of Lysergic Acid.
IV. Simple Lysergic Acid Amides
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Ergine-Erginine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. Lysergic Acid Methylcarbinolamide
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)C. Ergometrine-Ergometrinine
V. Peptide Alkaloids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Elucidation of Structure of the Peptide Portion
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. The Synthesis of Ergotamine and Its Stereochemistry
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)C. Characterization of the Ergot Alkaloids of the Peptide Type
VI. The Alkaloids of the Clavine Series
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Structural Relationships
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. The Clavine Alkaloids
VII. Biogenesis of the Ergot Alkaloids
VIII. Derivatives of Ergot Alkaloids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)A. Lysergic Acid and Dihydrolysergic Acid Derivatives of the Acid Amide Type
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)B. Amino and Carbamic Acid Derivatives of 6-Methylergolene and 6-Methylergoline
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)C. Substitutions in the Ring System of Lysergic Acid
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)D. Biological Oxidation of Lysergic Acid Derivatives
IX. The Pharmacology and Therapeutic Use of Ergot Alkaloids and Their Derivatives
References
The Indole Alkaloids
J. E. Saxton
in R.H.F. Manske's "The Alkaloids", Vol. 7, Ch. 10, p 1-37 (196?) (https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.indoles.pdf)
(https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.indoles.pdf)
Contents
I. Introduction
II. The Simple Bases
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)1. Gramine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)2. The Alkaloids of Piptadenia Species
III. The Ergot Alkaloids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)1. Introduction
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)2. Lysergic Acid, Isolysergic Acid, and the Dihydrolysergic Acids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)3. Stereochemistry of the Lysergic and Dihydrolysergic Acids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)4. Syntheses in the Lysergic Acid Series
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)5. Light-Transformation Products of the Ergot Alkaloids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)6. Biogenesis of Lysergic Acid
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)7. The Structure of the Peptide Half of the Ergot Alkaloids
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)8. Agroclavine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)9. Elymoclavine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)10. Penniclavine and Isopenniclavine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)11. Setoclavine, Isosetoclavine and Triseclavine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)12. Chanoclavine
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_docs/000481938-file_fdlo.gif)13. Miscellaneous Alkaloids
References