Amino Acids, Peptides and Proteins in Organic Chemistry Volume 4 - Protection Reactions, Medicinal Chemistry, Combinatorial Synthesis Amino Acids, Peptides and Proteins in Organic Chemistry (Volume 4) Edited by Hughes, Andrew B.
  1. Edition - March 2011 159.- Euro* 2011. XX, 532 Pages, Hardcover 319 Fig. (4 Colored Fig.), 25 Tab. - Handbook/Reference Book - ISBN-10: 3-527-32103-9 ISBN-13: 978-3-527-32103-2 - Wiley-VCH, Weinheim
* Series price on request at service@wiley-vch.de

Content
Sample Chapter
Index
Short description Closing a gap in the literature, this practical book series in 6 volumes draws on the expertise of the "who's who" in amino acid research to provide a comprehensive discussion of the occurrence, uses and applications of amino acids, their polymeric forms, peptides and proteins.
From the contents PROTECTION REACTIONS General Considerations Alpha-Amino Protection (Nalpha-Protection) Carboxy Protection Side Chain Protection Photocleavable Protections Conclusions Experimental Procedures
PART I: Amino Acid-Based Peptidomimetics
THE HUISGEN CYCLOADDITION IN PEPTIDOMIMETIC CHEMISTRY Introduction Huisgen [2+3] Cycloaddition Between Azides and Acetylenes Mechanistic Consideration for the Cu-Huisgen and Ru-Huisgen Cycloaddition Building Blocks for the Synthesis of TriazoleModified Peptidomimetics Cyclic Triazole Peptidomimetics Acylic Triazole Peptidomimetics Useful Experimental Procedures
RECENT ADVANCES IN BETA-STRAND MIMETICS Introduction Macrocyclic Peptidomimetics Acyclic Compounds Aliphatic and Aromatic Carbocycles Ligands Containing One Ring with One Heteroatom (N) Ligands Containing One Ring or Multiple Rings with One Heteroatom (O,S) Ligands Containing One Ring with Two Heteroatoms (N,N) Ligands Containing One Ring with Two Heteroatoms (N,S) or Three Heteroatoms (N,N,S or N,N,N) Ligands Containing Two Rings with One Heteroatom (N or O) Ligands Containing Two Rings with Two or Three Heteroatoms (N,N or N,S or N,N,N) Conclusions
PART II: Medicinal Chemistry of Amino Acids
MEDICINAL CHEMISTRY OF ALPHA-AMINO ACIDS Introduction Glutamic Acid Conformational Restriction Bioisosterism Structure-Activity-Studies Conclusions
MEDICINAL CHEMISTRY OF ALICYCLIC BETA-AMINO ACIDS Introduction Five-Membered Alicyclic Beta-Amino Acids Six-Membered Alicyclic Beta-Amino Acids
MEDICINAL CHEMISTRY OF ALPHA-HYDROXY-BETA-AMINO ACIDS Introduction Alpha-Hydroxy-Beta-Amino Acids Antibacterial Agents Inhibitors of Aminopeptidases Aspartyl Proteases Inhibitors Paclitaxel and its Derivatives
PEPTIDE DRUGS Lights and Shades of Peptide and Protein Drugs Peptide Drugs Available on the Market Approved Peptides in Oncology Antimicrobial Peptides Perspectives
ORAL BIOAVAILABILITY OF PEPTIDE AND PEPTIDOMIMETIC DRUGS Introduction Fundamental Considerations of Intestinal Absorption Barriers Limiting Oral Peptide/Peptidomimetic Drug Bioavailability Strategies to Improve Oral Bioavailability of Peptide-Based Drugs Conclusions
ASYMMETRIC SYNTHESIS OF BETA-LACTAMS VIA THE STAUDINGER REACTION Introduction Staudinger Reaction Influence of the Geometry of the Imine on Stereoselectivity in the Reaction Influence of the Polarity of the Solvent on Stereoselectivity of the Reaction Influence of the Isomerization of the Imine Prior to its Nucleophilic Attack onto the Ketene Stereoselectivity in the Reaction Influence of the Order of Addition of the Reactants to the Reaction Influence of Chiral Substituents on the Stereoselectivity of the Reaction Asymmetric Induction from the Imine Component Asymmetric Induction from the Ketene Component Double Asymmetric Cycloinduction Influence of Catalysts on the Stereoselectivity of the Reaction Concludings
ADVANCES IN N- AND O-GLYCOPEPTIDE SYNTHESIS - A TOOL TO STUDY CLYCOSYLATION AND DEVELOP NEW THERAPEUTICS Introduction Synthesis of O-Glycopeptides Synthesis of N-Glycopeptides
RECENT DEVELOPMENTS IN NEOGLYCOPEPTIDE SYNTHESIS Introduction Neoglycoside and Neoglycopeptide Synthesis Protein Side-Chain Modifications Cu(I)-Catalyzed Azide-Alkyne "Click" Cycloaddition Cross-Metathesis Application of Neoglycopeptides as Synthetic Vaccines Enzymatic, Molecular and Cell Biological Techniques
PART III: Amino Acids in Combinatorial Synthesis
COMBINATORIAL/LIBRARY PEPTIDE SYNTHESIS Introduction High-Throughput Synthesis of Peptides Synthesis of Peptide Arrays Peptide Libraries Future of Peptide Libraries Synthetic Protocols
PHAGE-DISPLAYED COMBINATORIAL PEPTIDES Introduction Conclusions
DESIGNING NEW PROTEINS Introduction Protein Design Methods Protocol for Protein Design Conclusions
AMINO ACID-BASED DENDRIMERS Introduction Peptide Dendrimer Synthesis: Divergent and Convergent Approaches Applications of Peptide Dendrimers Conclusions
|