Combinatorial Chemistry on Solid Supports
Themodernbillion-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 1980...
Enregistré dans:
| Hovedforfatter: | |
|---|---|
| Andre forfattere: | |
| Format: | Livre numérique |
| Sprog: | Anglais |
| Udgivet: |
Berlin, Heidelberg :
Springer Berlin Heidelberg
[20..].
Cham : Springer Nature |
| Udgivelse: | 1st ed. 2007. |
| Serier: | Topics in Current Chemistry
278 |
| Fag: | |
| Online adgang: | Accès sur la plateforme de l'éditeur Accès sur la plateforme Istex Accès Université d'Orléans Accès INSA CVL |
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Archives Springer e-books (Licence nationale) Archives Springer e-books (Licence nationale) |
| Autres localisations: | Voir dans le Sudoc |
| Variante du titre: | With contributions by numerous experts |
| Edition sous un autre format: | • Combinatorial chemistry on solid supports, volume editor : Stefan Bräse, Berlin, Springer Verlag, 2007, 1 vol. (X-360 p.), Topics in current chemistry, 3-540-72509-1 |
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| 020 | |a 9783540725107 | ||
| 041 | 0 | |a eng | |
| 082 | |a 547 | ||
| 082 | |a 540 | ||
| 100 | 1 | |a Braese, Stefan. | |
| 240 | 1 | 0 | |a With contributions by numerous experts |
| 245 | 1 | 0 | |a Combinatorial Chemistry on Solid Supports |c edited by Stefan Braese. |
| 250 | |a 1st ed. 2007. | ||
| 260 | |a Berlin, Heidelberg : |b Springer Berlin Heidelberg. | ||
| 260 | |a Cham : |b Springer Nature, |c [20..]. | ||
| 490 | 0 | |a Topics in Current Chemistry |v 278 |x 1436-5049 | |
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 500 | |a Archives Springer e-books (Licence nationale) | ||
| 505 | 1 | |a Multifunctional 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) | |
| 506 | |a Accès en ligne pour les établissements français bénéficiaires des licences nationales | ||
| 506 | |a Accès soumis à abonnement pour tout autre établissement | ||
| 506 | |a Conditions particulières de réutilisation pour les bénéficiaires des licences nationales. https://www.licencesnationales.fr/springer-nature-ebooks-contrat-licence-ln-2017 | ||
| 520 | |a Themodernbillion-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 Bräse group (Jung, Wiehn, Bräse) 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 | ||
| 650 | |a Chimie pharmaceutique | ||
| 650 | |a Chimie organométallique | ||
| 650 | |a Synthèse en phase solide | ||
| 650 | |a Chimie | ||
| 650 | |a Chimie organique | ||
| 650 | |a Biochimie | ||
| 650 | |a Chimie combinatoire | ||
| 700 | 1 | |a Bräse, Stefan. |4 edt | |
| 776 | 0 | |0 118877429 |t Combinatorial chemistry on solid supports |f volume editor : Stefan Bräse |c Berlin |n Springer Verlag |d 2007 |p 1 vol. (X-360 p.) |s Topics in current chemistry |z 3-540-72509-1 | |
| 856 | 4 | |q PDF |u https://doi.org/10.1007/978-3-540-72510-7 |z Accès sur la plateforme de l'éditeur | |
| 856 | 4 | |u https://revue-sommaire.istex.fr/ark:/67375/8Q1-RF2K3D5Z-C |z Accès sur la plateforme Istex | |
| 856 | 4 | |5 452349901:74788305X |u https://ezproxy.univ-orleans.fr/login?url=https://dx.doi.org/10.1007/978-3-540-72510-7 |z Accès Université d'Orléans | |
| 856 | 4 | |5 180339901:750895683 |u https://ezproxy.insa-cvl.fr/login?qurl=https://dx.doi.org/10.1007/978-3-540-72510-7 |z Accès INSA CVL | |
| 997 | |0 939345 |1 Livre numérique |a Ressource numérique |b INSA |b ENSA |c 0/Bibliothèque numérique/ |c 1/Bibliothèque numérique/Autre ressource numérique/ | ||