{"product_id":"activating-agents-and-protecting-groups-isbn-9780471979272","title":"Activating Agents and Protecting Groups","description":"Recognising the need for a cost effective reference work that deals not only with the most popular reagents in synthesis but also reaches the widest possible audience of practising organic chemists, the editors of 'The Encyclopedia of Reagents for Organic Synthesis' (EROS) have developed a list of the most important and useful reagents employed in the field, conveniently presented in four separate volumes.\u003cbr\u003e \u003cbr\u003e The reagents included in this volume reflect the fact that protecting groups and activation procedures are often used in combination. There are many instances in the synthesis of natural and unnatural products, pharmaceuticals, oligosaccharides, and oligonucleotides, etc., where similar tactics must be employed to prevent undesired activation or reaction of functionality. Accordingly, the most important reagents used to protect amines, alcohols, carboxyl, carbonyl and other reactive functional groups are included in this volume. The list of activating agents includes well known reagents that activate functional groups for substitution or elimination reactions, as well as less traditional examples, e.g. HMPA used to \"activate\" enolates and alkyllithium reagents to increase the nucleophilicity.\u003cbr\u003e \u003cbr\u003e Each article contains all of the information found in EROS as well as expanded related reagents listings and additional references to enable the reader to quickly access a broad range of information that is beyond the scope of the reagent entries themselves. This text will prove an invaluable resource.Aus dem bestehenden Material der \"Encyclopedia of Reagents for Organic Synthesis\" (EROS) werden Paquette und die Herausgeber 500 bevorzugte Reagenzien auswählen, die dann in 4 Bände entsprechend ihrer Klassifikation eingeteilt werden, z.B. Oxidations- und Reduktionsreagenzien. Die endgültigen Titel der Bände werden festgelegt, sobald die Auswahl der 500 Reagenzien vorgenommen wurde.\u003cbr\u003e Jeder Band wird sich in Umfang und Struktur an EROS orientieren, d.h. er verfügt über eine Einleitung, die ausgewählten Reagenzien erscheinen in alphabetischer Reihenfolge, und es gibt jeweils einen Index zu Reagenzien, Autoren und Themenkomplexen. Für jedes Reagenz werden die physikalischen und chemischen Daten detailliert angegeben, so daß der Leser den Gebrauch der jeweiligen Reagenz versteht und sicher mit ihr arbeiten kann. (01\/99) Partial table of contents:\u003cbr\u003e \u003cbr\u003e Acetic Anhydride.\u003cbr\u003e \u003cbr\u003e Acetyl Chloride (+ co-reactants).\u003cbr\u003e \u003cbr\u003e Aluminum Chloride.\u003cbr\u003e \u003cbr\u003e Boron Trifluorideetherate.\u003cbr\u003e \u003cbr\u003e Bromodimethylborane.\u003cbr\u003e \u003cbr\u003e 2,2-Dimethyl-1,3-propanediol.\u003cbr\u003e \u003cbr\u003e Dimethyl Sulfate.\u003cbr\u003e \u003cbr\u003e Diphenylbis(1,1,1,3,3,3-hexafluoro-2-phenyl-2-propoxy)-sulfirane.\u003cbr\u003e \u003cbr\u003e Ethylaluminum Dichloride.\u003cbr\u003e \u003cbr\u003e N-Ethylbenzisoxazolium Tetrafluoroborate.\u003cbr\u003e \u003cbr\u003e Hydrazine.\u003cbr\u003e \u003cbr\u003e 1-Hydroxybenzotriazole.\u003cbr\u003e \u003cbr\u003e Lithium Bromide.\u003cbr\u003e \u003cbr\u003e Lithium Chloride.\u003cbr\u003e \u003cbr\u003e Lithium Iodide.\u003cbr\u003e \u003cbr\u003e Montmorillonite K-10.\u003cbr\u003e \u003cbr\u003e 2-Morpholinoethyl Isocyanide.\u003cbr\u003e \u003cbr\u003e Phenyl Phosphorodi(1-imidazolate).\u003cbr\u003e \u003cbr\u003e Phosgene.\u003cbr\u003e \u003cbr\u003e 1,3-Propanediol.\u003cbr\u003e \u003cbr\u003e 1,3-Propanedithiol.\u003cbr\u003e \u003cbr\u003e Silver(I) Tetrafluoroborate.\u003cbr\u003e \u003cbr\u003e Triethylaluminum.\u003cbr\u003e \u003cbr\u003e Triethyl Orthoformate.\u003cbr\u003e \u003cbr\u003e Trifluoroacetic Anhydride.\u003cbr\u003e \u003cbr\u003e Zinc Bromide.\u003cbr\u003e \u003cbr\u003e Zinc Chloride.\u003cbr\u003e \u003cbr\u003e Zinc Iodide.\u003cbr\u003e \u003cbr\u003e Zinc Bis(p-toluenesulfonate).\u003cbr\u003e \u003cbr\u003e List of Contributors.\u003cbr\u003e \u003cbr\u003e Indexes.  \u003cp\u003eAnthony J. Pearson and William R. Roush are the authors of Activating Agents and Protecting Groups, published by Wiley.  Activating Agents and Protecting Groups A. J. Pearson Case Western University, Ohio, USA W. R. Roush University of Michigan, USA Recognising the critical need for bringing a handy reference work that deals with the most popular reagents in synthesis to the laboratory of practising organic chemists, the Editors of the acclaimed Encyclopedia of Reagents for Organic Synthesis (EROS) have selected the most important and useful reagents employed in contemporary organic synthesis. The reagents included in this volume reflect the fact that protecting groups and activation procedures are often used in combination. Accordingly, the most important reagents used to protect amines, alcohols, carboxyl, carbonyl and other reactive functional groups are included in this volume. The list of activating agents includes well known reagents that activate functional groups for substitution or elimination reactions, as well as less traditional examples, e.g. HMPA used to \"activate\" enolates and alkyllithium reagents to increase the nucleophilicity. Each article contains all of the information found in EROS as well as expanded related reagents listings and additional references to enable the reader to quickly access a broad range of information that is beyond the scope of the reagent entries themselves. This text will prove to be an invaluable resource.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47988657258725,"sku":"NP9780471979272","price":308.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9780471979272.jpg?v=1761781145","url":"https:\/\/k12savings.com\/products\/activating-agents-and-protecting-groups-isbn-9780471979272","provider":"K12savings","version":"1.0","type":"link"}