Cargando…

The isoquinoline alkaloids: chemistry and pharmacology /

The Isoquinoline Alkaloids Chemistry and Pharmacology.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Shamma, Maurice, 1926-
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York : Academic Press, [1972]
Colección:Organic chemistry (New York, N.Y.) ; v. 25.
Temas:
Acceso en línea:Texto completo
Texto completo
Tabla de Contenidos:
  • Front Cover; The Isoquinoline Alkaloids: Chemistry and Pharmacology; Copyright Page; Table of Contents; Preface; Chapter 1. THE SIMPLE TETRAHYDROISOQUINOLINES; I. Introduction; II. Degradations; III. Some Nonbasic Isoquinolines: Peyoglutam, Mescalotam, and Related Alkaloids; IV. Methods of Synthesis; V. The Gigantine Problem; VI. Some Reactions of Tetrahydroisoquinolines and Their Derivatives; VII. Absolute Configuration; VIII. Biosynthesis; IX. Pharmacology; X. The Possible Role of Tetrahydroisoquinoline Alkaloids in Alcoholism; XI. Mass Spectroscopy; XII. NMR Spectroscopy
  • XIII. UV SpectroscopyReferences; Chapter 2. THE BENZYLISOQUINOLINES; I. Introduction; II. Degradation of Laudanosine, A Tetrahydrobenzylisoquinoline Alkaloid; III. Structural Elucidation of Takatonine, A Quaternary Benzylisoquinoline Alkaloid; IV. Petaline, A Tetrahydrobenzylisoquinoline of Unusual Substitution Pattern; V. Two Glycosidic Tetrahydrobenzylisoquinoline Alkaloids: Latericine and Veronamine; VI. Methods of Synthesis; VII. Some Reactions of Benzylisoquinolines; VIII. Absolute Configuration; IX. Biosynthesis; X. Pharmacology
  • XI. A Possible Biochemical Basis for Alcohol Addiction: A Hypothesis and Its CritiqueXII. Mass Spectroscopy; XIII. NMR Spectroscopy; XIV. X-Ray Analysis; XV. UV Spectroscopy; References; Chapter 3. THE ISOQUINOLONES; I. Introduction; II. Structural Elucidation and Synthesis; III. An Alternate Synthesis of 3,4-Dihydroisoquinolones; IV. Pharmacology; References; Chapter 4. THE PA VINES AND ISOPAVINES; I. Structural Elucidation and Synthesis; II. Absolute Configuration; III. Biosynthesis; IV. Mass Spectroscopy; V. NMR Spectroscopy; VI. UV Spectroscopy
  • VII. The Differentiation between Pavine and Isopavine BasesReferences; Chapter 5. THE BISBENZYLISOQUINOLINES; I. Introduction; II. A Classical Degradation of a Bisbenzylisoquinoline Alkaloid: The Structure of Berbamine; III. Some Comments on the Sodium in Liquid Ammonia Cleavage of Bisbenzylisoquinolines; IV. The Structures of Tubocurarine, Chondocurarine, and Chondocurine; V. Repanduline: A Ketonic Bisbenzylisoquinoline Alkaloid; VI. Syntheses of Bisbenzylisoquinolines; VII. Conversion of Oxyacanthine-type Alkaloids to the Trilobine Series
  • VIII. Some Reagents for Interrelating Benzylisoquinolines, Bisbenzylisoquinolines, and Other IsoquinolinesIX. Biogenesis and Phenolic Oxidative Coupling; X. Pharmacology; XI. Absolute Configuration; XII. The Isomerization of (+)-Oxyacanthine to (
  • )-Repandine; XIII. Mass Spectroscopy; XIV. NMR Spectroscopy; XV. UV Spectroscopy; References; Chapter 6. THE CULARINES; I. Introduction; II. Cularine: Structural Determination; III. Syntheses of Cularine and Its Analogs; IV. Absolute Configuration; V. NMR Spectroscopy and Conformation; VI. Mass Spectroscopy; VII. UV Spectroscopy; References