Handbook of Reagents for Organic Synthesis
Vol. 4: Activating and Protecting Agents
Handbook of Reagents for Organic Synthesis

1. Auflage April 1999
XII, 514 Seiten, Hardcover
Wiley & Sons Ltd
Kurzbeschreibung
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.
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)
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.
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.
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.
Acetic Anhydride.
Acetyl Chloride (+ co-reactants).
Aluminum Chloride.
Boron Trifluorideetherate.
Bromodimethylborane.
2,2-Dimethyl-1,3-propanediol.
Dimethyl Sulfate.
Diphenylbis(1,1,1,3,3,3-hexafluoro-2-phenyl-2-propoxy)-sulfirane.
Ethylaluminum Dichloride.
N-Ethylbenzisoxazolium Tetrafluoroborate.
Hydrazine.
1-Hydroxybenzotriazole.
Lithium Bromide.
Lithium Chloride.
Lithium Iodide.
Montmorillonite K-10.
2-Morpholinoethyl Isocyanide.
Phenyl Phosphorodi(1-imidazolate).
Phosgene.
1,3-Propanediol.
1,3-Propanedithiol.
Silver(I) Tetrafluoroborate.
Triethylaluminum.
Triethyl Orthoformate.
Trifluoroacetic Anhydride.
Zinc Bromide.
Zinc Chloride.
Zinc Iodide.
Zinc Bis(p-toluenesulfonate).
List of Contributors.
Indexes.