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OverviewThemodernbillion-dollardrug-discoveryprocessstronglyreliesonbothhi- throughput synthesis and screening methods. Whereas the latter is based on molecular biological methods, the ef?cient and reliable generation of c- pound collections often makes use of combinatorial chemistry. Discovered in the 1980s, this methodology was explored extensively in the 1990s by groups in academia and in industry. Without any doubt, combinatorial chemistry changed the whole drug-discovery process and found many applications in cropscience and the material sciences. However, since its implementation, solution- and solid-phase techniques have been competing with each other, and although many companies started theircombinatorialchemistryprogramwithsolid-phasetechniques,soluti- phase combinatorial methods have taken over and now account for appro- mately 25% of all combinatorial efforts. The syntheses of complex, non-polymeric structures, discovered in the 1960s by the late Bruce Merri?eld, was largely ignored in the context of solid supports, mainly due to the fact that appropriate synthesis techniques were not available. Since solid-phase chemical methodology strongly differs from traditional solution-phase chemistry, two chapters deal with this topic. The Brase group (Jung, Wiehn, Brase) gives an overview of multifunctional linkers, which can beusedforthegenerationofdiversity-orientedcollections,simplybycleavage fromresins. Still in its infancy, solid-phase reactions employ ""simple"" amide chemistry in most cases due to their high-yielding, reliable protocols. Ljungdahl, Br- ?eld, and Kann address solid-phase organometallic chemistry, which is now one ofthe great challenges in reliable solid-phase organicsynthesis. Full Product DetailsAuthor: Stefan BraesePublisher: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG Imprint: Springer-Verlag Berlin and Heidelberg GmbH & Co. K Edition: Softcover reprint of hardcover 1st ed. 2007 Volume: 278 Dimensions: Width: 15.50cm , Height: 1.90cm , Length: 23.50cm Weight: 0.569kg ISBN: 9783642091551ISBN 10: 3642091555 Pages: 360 Publication Date: 25 November 2010 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: In Print ![]() This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsMultifunctional Linkers for Combinatorial Solid Phase Synthesis.- Solid Phase Organometallic Chemistry.- Solid Phase Chemistry for the Directed Synthesis of Biologically Active Polyamine Analogs, Derivatives, and Conjugates.- Combinatorial Solid-Phase Natural Product Chemistry.- Multiple Peptide Synthesis to Identify Bioactive Hormone Structures.- Automated Solid Phase Oligosaccharide Synthesis.- Probing Biology with Small Molecule Microarrays (SMM).ReviewsFrom the reviews: This book, written by an international group of renowned experts in their respective field, covers recent advances in important topics regarding combinatorial chemistry on solid supports. ! It will be a useful addition to the review literature and should be of interest to a significant segment of colleagues working in SPOC. (Rolando Perez-Pineiro and Hicham Fenniri, JACS, Vol. 130 (13), 2008) From the reviews: This book, written by an international group of renowned experts in their respective field, covers recent advances in important topics regarding combinatorial chemistry on solid supports. ... It will be a useful addition to the review literature and should be of interest to a significant segment of colleagues working in SPOC. (Rolando Perez-Pineiro and Hicham Fenniri, JACS, Vol. 130 (13), 2008) Author InformationTab Content 6Author Website:Countries AvailableAll regions |