The Isoquinoline Alkaloids: A Course in Organic Chemistry is a description of the chemical structures of alkaloids.
The book discusses the processes for degradation of isoquinoline alkaloids to recognizable compounds such as oxidation and exhaustive methylation. The associated processes in removing the nitrogen atom are also explained. The commonly used Hofmann process and the interpretation of its result are evaluated in the degradation of alkaloids. The cactus ""pellote"" used by Mexican Indians to induce hallucinatory experiences is examined. The active ingredient is identified as mescaline; its composition is analyzed to contain one primary amino and three methoxyl groups. The different syntheses made to duplicate mescaline are described. The structures of morphine, codeine, and thebain, which are all alkaloids of opium, are also analyzed. Another example of a principal alkaloid found in a plant is emetine found in the root of the ipecac. The pharmacological bases of emetine are isolated and noted as emetamine, cephaeline, psychotrine, and O-methylpsychotrine. The text also traces many other structural relationships within the subgroups of the isoquinoline alkaloids.
Chemists, students and professors in organic chemistry, and laboratory technicians whose work is related to pharmacology will find this book informative.
Chapter 1 Introduction
Chapter 2 β-Phenylethylamines and Simple Isoquinolines
Chapter 3 Benzylisoquinolines
Chapter 4 Bisbenzylisoquinolines
Chapter 5 Cularine
Chapter 6 The Aporphines
Chapter 7 The Morphine Alkaloids
Chapter 8 The Berberine and Tetrahydroberberine Alkaloids
Chapter 9 Alkaloids Related to Cryptopine
Chapter 10 Rhoeadine
Chapter 11 The Phthalideisoquinolines
Chapter 12 The α-Naphthaphenanthridines
Chapter 13 Emetine and Related Compounds
Chapter 14 The Biogenesis of the Isoquinoline Alkaloids
- No. of pages:
- © Pergamon 1965
- 1st January 1965
- eBook ISBN:
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