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Essential Reagents for Organic Synthesis.

From Boron Trifluoride to Zinc, the 52 most widely used reagents in organic synthesis are described in this unique desktop reference for every organic chemist. The list of reagents contains classics such as N-Bromosuccinimide (NBS) and Trifluoromethanesulfonic Acid side by side with recently develop...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Fuchs, Philip L.
Otros Autores: Charette, André B., Rovis, Tomislav, Bode, Jeffrey W.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Newark : Wiley, 2016.
Temas:
Acceso en línea:Texto completo

MARC

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505 0 |a Essential Reagents for Organic Synthesis; Contents; Preface; Short Note on InChIs and InChIKeys; General Abbreviations; Bis(dibenzylideneacetone)palladium(0); 9-Borabicyclo[3.3.1]nonane Dimer; Boron Trifluoride Etherate; N-Bromosuccinimide; n-Butyllithium; N, N'-Carbonyl Diimidazole; Cerium(IV) Ammonium Nitrate; m-Chloroperbenzoic Acid; N-Chlorosuccinimide; Chlorotrimethylsilane; Chlorotris(triphenylphosphine)-rhodium(I); (Diacetoxyiodo)benzene; Diazomethane; 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone; Diisobutylaluminum Hydride; 4-Dimethylaminopyridine; Dimethyldioxirane. 
505 8 |6 880-01  |a Sodium HydrideSodium Periodate; Tetrabutylammonium Fluoride; Tetrakis(triphenylphosphine)-palladium(0); Tetra-n-propylammonium Perruthenate; p-Toluenesulfonyl Chloride; Triethylsilane; Trifluoromethanesulfonic Acid; Trifluoromethanesulfonic Anhydride; Trimethylsilyl Trifluoromethanesulfonate; Trimethylsilyldiazomethane; Zinc-Acetic Acid; List of Contributors; Subject Index; End User License Agreement. 
520 |a From Boron Trifluoride to Zinc, the 52 most widely used reagents in organic synthesis are described in this unique desktop reference for every organic chemist. The list of reagents contains classics such as N-Bromosuccinimide (NBS) and Trifluoromethanesulfonic Acid side by side with recently developed ones like Pinacolborane and Tetra-n-propylammonium Perruthenate (TPAP). For each reagent, a concise article provides a brief description of all important reactions for which the reagent is being used, including yields and reaction conditions, an overview of the physical properties of the reagent, its storage conditions, safe handling, laboratory synthesis and purification methods. Advantages and disadvantages of the reagent compared to alternative synthesis methods are also discussed. Reagents have been hand-picked from among the 5000 reagents contained in EROS, the Encyclopedia of Reagents for Organic Synthesis. Every organic chemist should be familiar with these key reagents that can make almost every reaction work. 
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880 8 |6 505-01/(S  |a 1-Ethyl-3-(3 -dimethylaminopropyl)carbodiimide HydrochlorideN-Iodosuccinimide; Iodotrimethylsilane; 2-Iodoxybenzoic Acid; Lithium Aluminum Hydride; Lithium Diisopropylamide; Lithium Naphthalenide; Manganese Dioxide; Osmium Tetroxide; Oxalyl Chloride; Oxalyl Chloride-Dimethylformamide; Ozone; Pinacolborane; Potassium Hexamethyldisilazide; Potassium Monoperoxysulfate; Potassium tert-Butoxide; Ruthenium(II), Tris(2,2'-bipyridine-κN1,κN1')-, (OC-6-11); Samarium(II) Iodide; Scandium Trifluoromethanesulfonate; Sodium Azide; Sodium Borohydride; Sodium Cyanoborohydride; Sodium Hexamethyldisilazide. 
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