Principles of Peptide Synthesis

Detalles Bibliográficos
Autor principal: Bodanszky, Miklos. (Autor)
Autor Corporativo: SpringerLink (Online service)
Formato: eBook
Lenguaje:English
Publicado: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 1993.
Edición:2nd ed. 1993.
Colección:Springer Lab Manuals
Materias:
Acceso en línea:https://doi.org/10.1007/978-3-642-78056-1
Tabla de Contenidos:
  • I. Introduction
  • References
  • II. Activation and Coupling
  • 1 Activation
  • 2 Coupling
  • 3 Coupling Methods
  • References
  • III. Reversible Blocking of Amino and Carboxyl Groups
  • 1 General Aspects
  • 2 Protection of the Carboxyl Group
  • 3 Protection of the Amino Group
  • References
  • IV. Semipermanent Protection of Side Chain Functions
  • 1 Carboxyl Groups of Aspartyl and Glutamyl Residues
  • 2 Side Chain Amino Groups of Lysine and Ornithine
  • 3 Hydroxyl Groups in Serine, Threonine and Tyrosine
  • 4 The Sulfhydryl Group in Cysteine
  • 5 The Guanidino Group of Arginine
  • 6 Imidazole in Histidine
  • 7 The Thioether in Methionine
  • 8 The Indole Nitrogen in Tryptophan
  • 9 The Carboxamide Groups in Asparagine and Glutamine
  • References
  • V. Side Reactions in Peptide Synthesis
  • 1 Side Reactions Initiated by Proton Abstraction
  • 2 Side Reactions Initiated by Protonation
  • 3 Side Reactions Due to Overactivation
  • 4 Side Reactions Related to Individual Amino Acid Residues
  • References
  • VI. Tactics and Strategy in Peptide Synthesis
  • 1 Tactics
  • 2 Strategies
  • 3 Disulfide Bridges
  • 4 Synthesis of Cyclic Peptides
  • 5 Sequential Polypeptides
  • 6 Partial Synthesis (Semisynthesis)
  • References
  • VII. Techniques for the Facilitation of Peptide Synthesis
  • 1 Solid Phase Peptide Synthesis (SPPS)
  • 2 Synthesis in Solution
  • References
  • VIII Recent Developments, New Trends
  • 1 Formation of the Peptide Bond
  • 2 Protecting Groups
  • 3 Solid Phase Peptide Synthesis
  • 4 Undesired Reactions in Peptide Synthesis
  • 5 New Trends and Perspectives
  • References.