{"product_id":"comprehensive-reactions-in-aqueous-2e-9780471761297","title":"Comprehensive Reactions in Aqueous 2e","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eOrganic reactions in water have proven a useful synthetic tool, and provide cost-efficient, safe, and environmentally friendly alternatives to organic-solvent based reactions. This field has been greatly expanded over the last decade, and currently there are many diverse applications in both industry and academic laboratories.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTrade Review\u003c\/b\u003e\u003cbr\u003e\"As it is a conference report, the book is clearly intended for specialists in the field.\" (\u003ci\u003eAngewandte Chemie\u003c\/i\u003e, 2008-47\/11)  \u003cp\u003e\"…a testament to the enormous expansion in the field of water-based chemistry, and compiling it in a single volume is very useful.\" (\u003ci\u003eJournal of the American Chemical Society\u003c\/i\u003e, December 26, 2007)\u003c\/p\u003e \u003cp\u003e\"Advanced students and research and development chemists with an interest in green chemistry are highly recommended to purchase this book.\" (\u003ci\u003eOrganic Chemistry Portal\u003c\/i\u003e, January 2008)\u003c\/p\u003e\u003cbr\u003e\"Diese Aktualisierung einer klassischen Monographie fasst die bedeutenden Fortschritte auf dem Gebiet organischer Reaktionen in wassriger Phase in den letzten Jahren hervorragend zusammen.\"\u003cbr\u003e Angewandte Chemie\u003cbr\u003e 2008-120\/11\u003cbr\u003e\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cb\u003ePREFACE TO THE SECOND EDITION.\u003c\/b\u003e  \u003cp\u003e\u003cb\u003e1. INTRODUCTION.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 The Structure and Forms of Water.\u003c\/p\u003e \u003cp\u003e1.2 Properties of Water.\u003c\/p\u003e \u003cp\u003e1.3 Solvation.\u003c\/p\u003e \u003cp\u003e1.4 Hydrophobic Effect.\u003c\/p\u003e \u003cp\u003e1.5 Salt Effect.\u003c\/p\u003e \u003cp\u003e1.6 Water Under Extreme Conditions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e2. ALKANES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Oxygenation of Alkanes.\u003c\/p\u003e \u003cp\u003e2.2 Halogenation of Alkanes.\u003c\/p\u003e \u003cp\u003e2.3 Formation of Carbon–Carbon Bonds.\u003c\/p\u003e \u003cp\u003e2.4 D\/H Exchange of Alkanes in Water.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e3. ALKENES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Reduction.\u003c\/p\u003e \u003cp\u003e3.2 Electrophilic Additions.\u003c\/p\u003e \u003cp\u003e3.3 Radical Reactions of Alkenes.\u003c\/p\u003e \u003cp\u003e3.4 Carbene Reactions.\u003c\/p\u003e \u003cp\u003e3.5 Alkene Isomerization.\u003c\/p\u003e \u003cp\u003e3.6 Transition-Metal Catalyzed C–C Formation Reactions.\u003c\/p\u003e \u003cp\u003e3.7 Olefin Metathesis.\u003c\/p\u003e \u003cp\u003e3.8 Reaction of Allylic C–H Bond.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4. ALKYNES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Reaction of Terminal Alkynes.\u003c\/p\u003e \u003cp\u003e4.2 Additions of C≡C bonds.\u003c\/p\u003e \u003cp\u003e4.3 Transition-Metal Catalyzed Cycloadditions.\u003c\/p\u003e \u003cp\u003e4.4 Other Reactions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e5. ALCOHOLS, PHENOLS, ETHERS, THIOLS, AND THIOETHERS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Oxidation of Alcohols.\u003c\/p\u003e \u003cp\u003e5.2 Substitutions\/Elimination.\u003c\/p\u003e \u003cp\u003e5.3 Addition of Alcohols, Phenols, and Thiols to Alkene and Alkyne Bonds.\u003c\/p\u003e \u003cp\u003e5.4 Addition of Alcohols to C=O Bonds: Esterification and Acetal Formations.\u003c\/p\u003e \u003cp\u003e5.5 Reaction of Ethers and Cyclic Ethers.\u003c\/p\u003e \u003cp\u003e5.6 Reaction of Sulfur Compounds.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6. ORGANIC HALIDES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 General.\u003c\/p\u003e \u003cp\u003e6.2 Reduction.\u003c\/p\u003e \u003cp\u003e6.3 Elimination Reactions.\u003c\/p\u003e \u003cp\u003e6.4 Nucleophilic Substitutions.\u003c\/p\u003e \u003cp\u003e6.5 Reductive Coupling.\u003c\/p\u003e \u003cp\u003e6.6 Carbonylation of Organic Halides.\u003c\/p\u003e \u003cp\u003e6.7 Transition-Metal Catalyzed Coupling Reactions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e7. AROMATIC COMPOUNDS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e7.1 General.\u003c\/p\u003e \u003cp\u003e7.2 Substitution Reactions.\u003c\/p\u003e \u003cp\u003e7.3 Oxidation Reactions.\u003c\/p\u003e \u003cp\u003e7.4 Reductions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e8. ALDEHDYE AND KETONES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e8.1 Reduction.\u003c\/p\u003e \u003cp\u003e8.2 Oxidation.\u003c\/p\u003e \u003cp\u003e8.3 Nucleophilic Addition: C–C Bond Formation.\u003c\/p\u003e \u003cp\u003e8.4 Pinacol Coupling.\u003c\/p\u003e \u003cp\u003e8.5 Other Reactions (Halogenation and Oxidation of α-H).\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e9. CARBOXYLIC ACIDS AND DERIVATIVES.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e9.1 General.\u003c\/p\u003e \u003cp\u003e9.2 Carboxylic Acids.\u003c\/p\u003e \u003cp\u003e9.3 Carboxylic Acid Derivatives.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e10. CONJUGATED CARBONYL COMPOUNDS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10.1 Reduction.\u003c\/p\u003e \u003cp\u003e10.2 Epoxidation, Dihydroxylation, Hydroxyamination.\u003c\/p\u003e \u003cp\u003e10.3 Conjugate Addition: Heteroatom.\u003c\/p\u003e \u003cp\u003e10.4 C–C Bond Formation.\u003c\/p\u003e \u003cp\u003e10.5 Other Reactions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e11. NITROGEN COMPOUNDS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e11.1 Amines.\u003c\/p\u003e \u003cp\u003e11.2 Imines.\u003c\/p\u003e \u003cp\u003e11.3 Diazo Compounds.\u003c\/p\u003e \u003cp\u003e11.4 Azides.\u003c\/p\u003e \u003cp\u003e11.5 Nitro Compounds.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003e12. PERICYCLIC REACTIONS.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e12.1 Introduction.\u003c\/p\u003e \u003cp\u003e12.2 Diels-Alder Reactions.\u003c\/p\u003e \u003cp\u003e12.3 Sigmatropic Rearrangements.\u003c\/p\u003e \u003cp\u003e12.4 Photochemical Cycloaddition Reactions.\u003c\/p\u003e \u003cp\u003eReferences. \u003c\/p\u003e \u003cp\u003e\u003cb\u003eINDEX.\u003c\/b\u003e\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":52090689716567,"sku":"9780471761297","price":149.35,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9780471761297.jpg?v=1762273095","url":"https:\/\/bookcurl.com\/products\/comprehensive-reactions-in-aqueous-2e-9780471761297","provider":"Book Curl","version":"1.0","type":"link"}