Amino Acids, Peptides and Proteins in Organic Chemistry / Amino Acids, Peptides and Proteins in Organic Chemistry Bd.4 (PDF)
Volume 4 - Protection Reactions, Medicinal Chemistry, Combinatorial Synthesis
(Sprache: Englisch)
This is the fourth of five books in the Amino Acids, Peptides and Proteins in Organic Synthesis series.
Closing a gap in the literature, this is the only series to cover this important topic in organic and biochemistry. Drawing upon the combined...
Closing a gap in the literature, this is the only series to cover this important topic in organic and biochemistry. Drawing upon the combined...
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Produktinformationen zu „Amino Acids, Peptides and Proteins in Organic Chemistry / Amino Acids, Peptides and Proteins in Organic Chemistry Bd.4 (PDF)“
This is the fourth of five books in the Amino Acids, Peptides and Proteins in Organic Synthesis series.
Closing a gap in the literature, this is the only series to cover this important topic in organic and biochemistry. Drawing upon the combined expertise of the international "who's who" in amino acid research, these volumes represent a real benchmark for amino acid chemistry, providing a comprehensive discussion of the occurrence, uses and applications of amino acids and, by extension, their polymeric forms, peptides and proteins. The practical value of each volume is heightened by the inclusion of experimental procedures.
The fourth volume in this five-volume series is structured in three main sections. The first section is about protection reactions and amino acid-based peptidomimetics. The second, and most extensive, part is devoted to the medicinal chemistry of amino acids. It includes, among others, the chemistry of alpha- and beta amino acids, peptide drugs, and advances in N- and O-glycopeptide synthesis. The final part deals with amino acids in combinatorial synthesis. Methods, such as phage display, library peptide synthesis, and computational design are described.
Closing a gap in the literature, this is the only series to cover this important topic in organic and biochemistry. Drawing upon the combined expertise of the international "who's who" in amino acid research, these volumes represent a real benchmark for amino acid chemistry, providing a comprehensive discussion of the occurrence, uses and applications of amino acids and, by extension, their polymeric forms, peptides and proteins. The practical value of each volume is heightened by the inclusion of experimental procedures.
The fourth volume in this five-volume series is structured in three main sections. The first section is about protection reactions and amino acid-based peptidomimetics. The second, and most extensive, part is devoted to the medicinal chemistry of amino acids. It includes, among others, the chemistry of alpha- and beta amino acids, peptide drugs, and advances in N- and O-glycopeptide synthesis. The final part deals with amino acids in combinatorial synthesis. Methods, such as phage display, library peptide synthesis, and computational design are described.
Inhaltsverzeichnis zu „Amino Acids, Peptides and Proteins in Organic Chemistry / Amino Acids, Peptides and Proteins in Organic Chemistry Bd.4 (PDF)“
PROTECTION REACTIONS General Considerations Alpha-Amino Protection (Nalpha-Protection) Carboxy Protection Side Chain Protection Photocleavable Protections Conclusion Experimental Section THE HUISGEN CYCLOADDITION IN PEPTIDOMIMETIC CHEMISTRY Introduction The Huisgen [2+3] Cycloaddition Between Azides and Acetylenes Mechanistic Consideration for the Cu-Huisgen and Ru-Huisgen Cycloaddition Building Blocks for the Synthesis of Triazole Modified 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 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) Concluding Remarks MEDICINAL CHEMISTRY OF ALPHA-AMINO ACIDS Introduction Glutamic Acid Conformational Restriction Bioisosterism Structure-Activity-Studies Conclusion 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 Drugs Bioavailability Strategies to Improve Peptide-Based Drugs Oral Bioavailability Conclusions
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ASYMMETRIC SYNTHESIS OF BETA-LACTAMS VIA THE STAUDINGER REACTION Introduction The 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 Concluding Remarks ADVANCES IN N- AND O-GLYCOPEPTIDE SYNTHESIS - A TOOL TO STUDY CLYCOSYLATION AND DEVELOP NEW THERAPEUTICS Introduction O-Glycopeptide Synthesis Synthesis of Mucin Type Glycopeptides Synthesis of Tumor-Associated Glycopeptides and Glycopeptide Vaccines Synthesis of Tn, T, sialyl Tn, sialyl T Glycosylated Amino Acid Building Blocks Synthesis of Tn, T, sialyl Tn, sialyl T Glycopeptides and Vaccines Synthesis of Glycopeptide Recognition Domain of P-Selectin Glycoprotein Ligand 1 (PSGL-1) Synthesis of a Core 2 sLe AMino Acid Building Block Including a sLe Mimic Synthesis of Unsulfated and Sulfated Core 2 sLe and Core 2 sLe Mimic PSGL-1 Glycopeptides Chemoenzymatic Synthesis of Unsulphated and Sulphated Sialyl Lewis PSGL-1 Glycopeptide Synthesis of Other Types of O-Glycopeptides Synthesis of Fmoc-GlcNAc-Ser/Thr Amino Acids Synthesis of Estrogene Receptor Peptides for Conformational Analysis Synthesis of N-Glycopeptides Synthesis of Ribonuclease C (RNase C) Glycoprotein Synthesis of Erythropoietin N-Glycopeptide Fragment 1-28 Synthesis of Biantennary Dodecasaccharide Synthesis of N-Glycopeptide Fragment 1-28 Chemoenzymatic Synthesis of a HIV GP120 V3 Domain N-Glycopeptide Synthesis of the Oxazoline Tetrasaccharide Donor Synthesis of Fmoc-GlcNAc-Asn Amino
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Autoren-Porträt
Andrew Hughes is a Reader and Head of the Department of Chemistry, La Trobe University, Melbourne, Australia. He obtained his degrees from the University of Western Australia. Post-doctoral appointments at the University of Cambridge starting 1989 included 3 years working with Professor Andrew Holmes before joining Professor Steven Leys group in 1993. While at Cambridge he was appointed the Shell Research Fellow at Robinson College.
Bibliographische Angaben
- 2011, 1. Auflage, 532 Seiten, Englisch
- Verlag: Wiley-VCH GmbH
- ISBN-10: 3527631836
- ISBN-13: 9783527631834
- Erscheinungsdatum: 25.05.2011
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