Vol . 2, No. 4 Unnatural Amino Acids II The latest Update on New Tools for Drug Discovery Click here to download PDF version. (688 KB)
Introduction / Cyclic Amino Acids / Diamino Acids / ß-Amino Acids and Homo Amino Acids Alanine Derivatives / Phenylalanine Boronic Acids / Proline and Pyroglutamine Derivatives Other Amino Acid Building Blocks / Coupling Reagents / Preloaded Resins / Books Books
Fmoc Solid Phase Peptide Synthesis: A Practical Approach
W.C. Chan and P.D. White, Eds., Oxford University Press, New York, NY, 2000, 376pp. Hardcover.
Covers not only the essential procedures for the production of linear peptides but also more advanced techniques for preparing cyclic, side-chain modified, phospho- and glycopeptides. Many other methods also deserving attention have been included: convergent peptide synthesis; peptide-protein conjugation; chemoselective ligation; and chemoselective purification.
Z42,426-9
A Practical Guide to Combinatorial Chemistry
A.W. Czarnik and S.H. DeWitt, Eds., American Chemical Society, Washington, DC, 1997, 450pp. Hardcover.
A practical guide for both newcomers and specialists in small-molecule combinatorial chemistry. Tutorial-style chapters review computational tools to analyze molecular diversity, methods of solid-phase peptide and small-molecule synthesis, and approaches to synthesizing solid- and solution-phase libraries.
Z40,842-5
Combinatorial Peptide and Nonpeptide Libraries: A Handbook
G. Jung, John Wiley & Sons, New York, NY, 1997, 545pp. Hardcover.
The use of combinatorial chemistry and peptide libraries in drug screening and development is a new and rapidly expanding technology. This first handbook on the topic contains background information and step-by-step experimental procedures.
Z28,816-0
Compendium of Chiral Auxiliary Applications, 3-volume set
Greg Roos, Sultan Qaboos University, Sultanate of Oman. Hardback 1612 Pages. Academic Press. Published December 2001
This is the first major reference work of its kind to look logically and sequentially at Chiral Auxiliaries, investigating their properties and applications in diastereoselective synthesis.
- Fully cross-referenced to enable comparative selection of auxiliaries to be made dependent on target application
- Includes more than 13,000 auxiliary reaction applications with complete reaction details for each auxiliary.
Z51,324-5
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