{"product_id":"named-organic-reactions-paperback-softback-9780470010419","title":"Named Organic Reactions (Paperback \/ softback) 9780470010419","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eNamed Organic Reactions\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eThomas Laue (Author), Andreas Plagens (Author)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470010419, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003ePaperback \/ softback, published 18 February 2005\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e320 pages\u003cbr\u003e23.1 x 15.2 x 1.8 cm, 0.454 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cem\u003e\u003cfont size=\"3\"\u003e\"…the clarity of the text and the extensive coverage would make this an excellent book for a graduate student or upper level chemistry major. Practicing organic chemists…might also find it a worthy addition to their personal libraries.\" (\u003ci\u003eJournal of Medicinal Chemistry\u003c\/i\u003e, January 26, 2006)  \u003cp\u003e\"…an indispensable resource…the essential nature of each of the reactions addressed in the book is presented in sufficient detail…\" (\u003ci\u003eJournal of Chemical Education\u003c\/i\u003e, December 2005)\u003c\/p\u003e \u003cp\u003e\"This book is an essential guide to named organic reactions for chemistry students, organic chemists, and chemists in general.\" (\u003ci\u003eChemical Educator\u003c\/i\u003e, May\/June 2005)\u003c\/p\u003e\u003c\/font\u003e\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eThis Second edition contains consise information on 134 carefully chosen named organic reactions - the standard set of undergraduate and graduate synthetic organic chemistry courses. Each reaction is detailed with clearly drawn mechanisms, references from the primary literature, and well-written accounts covering the mechanical aspects of the reactions, and the details of side reactions and substrate limitations. For the 2nd edition the complete text has been revised and updated, and four new reactions have been added: Baylis-Hillmann Reaction, Sonogashira Reaction, Pummerer Reaction, and the Swern Oxidation und Cyclopropanation. An essential text for students preparing for exams in organic chemistry.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003ci\u003eIntroduction to the 2nd Edition.\u003c\/i\u003e  \u003cp\u003eAcyloin Ester Condensation.\u003c\/p\u003e \u003cp\u003eAldol Reaction.\u003c\/p\u003e \u003cp\u003eAlkene Metathesis.\u003c\/p\u003e \u003cp\u003eArbuzov Reaction.\u003c\/p\u003e \u003cp\u003eArndt–Eistert Synthesis.\u003c\/p\u003e \u003cp\u003eBaeyer–Villiger Oxidation.\u003c\/p\u003e \u003cp\u003eBamford–Stevens Reaction.\u003c\/p\u003e \u003cp\u003eBarton Reaction.\u003c\/p\u003e \u003cp\u003eBaylis–Hillman Reaction.\u003c\/p\u003e \u003cp\u003eBeckmann Rearrangement.\u003c\/p\u003e \u003cp\u003eBenzidine Rearrangement.\u003c\/p\u003e \u003cp\u003eBenzilic Acid Rearrangement.\u003c\/p\u003e \u003cp\u003eBenzoin Condensation.\u003c\/p\u003e \u003cp\u003eBergman Cyclization.\u003c\/p\u003e \u003cp\u003eBirch Reduction.\u003c\/p\u003e \u003cp\u003eBlanc Reaction.\u003c\/p\u003e \u003cp\u003eBucherer Reaction.\u003c\/p\u003e \u003cp\u003eCannizzaro Reaction.\u003c\/p\u003e \u003cp\u003eChugaev Reaction.\u003c\/p\u003e \u003cp\u003eClaisen Ester Condensation.\u003c\/p\u003e \u003cp\u003eClaisen Rearrangement.\u003c\/p\u003e \u003cp\u003eClemmensen Reduction.\u003c\/p\u003e \u003cp\u003eCope Elimination Reaction.\u003c\/p\u003e \u003cp\u003eCope Rearrangement.\u003c\/p\u003e \u003cp\u003eCorey–Winter Fragmentation.\u003c\/p\u003e \u003cp\u003eCurtius Reaction.\u003c\/p\u003e \u003cp\u003e1,3-Dipolar Cycloaddition.\u003c\/p\u003e \u003cp\u003e[\u003cb\u003e\u003ci\u003e2\u003c\/i\u003e\u003c\/b\u003e\u003cb\u003eY\u003c\/b\u003e\u003cb\u003e\u003ci\u003e2\u003c\/i\u003e\u003c\/b\u003e ] Cycloaddition.\u003c\/p\u003e \u003cp\u003eDarzens Glycidic Ester Condensation.\u003c\/p\u003e \u003cp\u003eDel´epine Reaction.\u003c\/p\u003e \u003cp\u003eDiazo Coupling.\u003c\/p\u003e \u003cp\u003eDiazotization.\u003c\/p\u003e \u003cp\u003eDiels–Alder Reaction.\u003c\/p\u003e \u003cp\u003eDi-p-Methane Rearrangement.\u003c\/p\u003e \u003cp\u003eD¨otz Reaction.\u003c\/p\u003e \u003cp\u003eElbs Reaction.\u003c\/p\u003e \u003cp\u003eEne Reaction.\u003c\/p\u003e \u003cp\u003eEster Pyrolysis.\u003c\/p\u003e \u003cp\u003eFavorskii Rearrangement.\u003c\/p\u003e \u003cp\u003eFinkelstein Reaction.\u003c\/p\u003e \u003cp\u003eFischer Indole Synthesis.\u003c\/p\u003e \u003cp\u003eFriedel–Crafts Acylation.\u003c\/p\u003e \u003cp\u003eFriedel–Crafts Alkylation.\u003c\/p\u003e \u003cp\u003eFriedl¨ander Quinoline Synthesis.\u003c\/p\u003e \u003cp\u003eFries Rearrangement.\u003c\/p\u003e \u003cp\u003eGabriel Synthesis.\u003c\/p\u003e \u003cp\u003eGattermann Synthesis.\u003c\/p\u003e \u003cp\u003eGlaser Coupling Reaction.\u003c\/p\u003e \u003cp\u003eGlycol Cleavage.\u003c\/p\u003e \u003cp\u003eGomberg–Bachmann Reaction.\u003c\/p\u003e \u003cp\u003eGrignard Reaction.\u003c\/p\u003e \u003cp\u003eHaloform Reaction.\u003c\/p\u003e \u003cp\u003eHantzsch Pyridine Synthesis.\u003c\/p\u003e \u003cp\u003eHeck Reaction.\u003c\/p\u003e \u003cp\u003eHell–Volhard–Zelinskii Reaction.\u003c\/p\u003e \u003cp\u003eHofmann Elimination Reaction.\u003c\/p\u003e \u003cp\u003eHofmann Rearrangement.\u003c\/p\u003e \u003cp\u003eHunsdiecker Reaction.\u003c\/p\u003e \u003cp\u003eHydroboration.\u003c\/p\u003e \u003cp\u003eJapp-Klingemann Reaction.\u003c\/p\u003e \u003cp\u003eKnoevenagel Reaction.\u003c\/p\u003e \u003cp\u003eKnorr Pyrrole Synthesis.\u003c\/p\u003e \u003cp\u003eKolbe Electrolytic Synthesis.\u003c\/p\u003e \u003cp\u003eKolbe Synthesis of Nitriles.\u003c\/p\u003e \u003cp\u003eKolbe–Schmitt Reaction.\u003c\/p\u003e \u003cp\u003eLeuckart–Wallach Reaction.\u003c\/p\u003e \u003cp\u003eLossen Reaction.\u003c\/p\u003e \u003cp\u003eMalonic Ester Synthesis.\u003c\/p\u003e \u003cp\u003eMannich Reaction.\u003c\/p\u003e \u003cp\u003eMcMurry Reaction.\u003c\/p\u003e \u003cp\u003eMeerwein–Ponndorf–Verley Reduction.\u003c\/p\u003e \u003cp\u003eMichael Reaction.\u003c\/p\u003e \u003cp\u003eMitsunobu Reaction.\u003c\/p\u003e \u003cp\u003eNazarov Cyclization.\u003c\/p\u003e \u003cp\u003eNeber Rearrangement.\u003c\/p\u003e \u003cp\u003eNef Reaction.\u003c\/p\u003e \u003cp\u003eNorrish Type I Reaction.\u003c\/p\u003e \u003cp\u003eNorrish Type II Reaction.\u003c\/p\u003e \u003cp\u003eOzonolysis.\u003c\/p\u003e \u003cp\u003ePaterno–B¨uchi Reaction.\u003c\/p\u003e \u003cp\u003ePauson–Khand Reaction.\u003c\/p\u003e \u003cp\u003ePerkin Reaction.\u003c\/p\u003e \u003cp\u003ePeterson Olefination.\u003c\/p\u003e \u003cp\u003ePinacol Rearrangement.\u003c\/p\u003e \u003cp\u003ePrilezhaev Reaction.\u003c\/p\u003e \u003cp\u003ePrins Reaction.\u003c\/p\u003e \u003cp\u003eRamberg–B¨acklund Reaction.\u003c\/p\u003e \u003cp\u003eReformatsky Reaction.\u003c\/p\u003e \u003cp\u003eReimer–Tiemann Reaction.\u003c\/p\u003e \u003cp\u003eRobinson Annulation.\u003c\/p\u003e \u003cp\u003eRosenmund Reduction.\u003c\/p\u003e \u003cp\u003eSakurai Reaction.\u003c\/p\u003e \u003cp\u003eSandmeyer Reaction.\u003c\/p\u003e \u003cp\u003eSchiemann Reaction.\u003c\/p\u003e \u003cp\u003eSchmidt Reaction.\u003c\/p\u003e \u003cp\u003eSharpless Epoxidation.\u003c\/p\u003e \u003cp\u003eSimmons–Smith Reaction.\u003c\/p\u003e \u003cp\u003eSkraup Quinoline Synthesis.\u003c\/p\u003e \u003cp\u003eStevens Rearrangement.\u003c\/p\u003e \u003cp\u003eStille Coupling Reaction.\u003c\/p\u003e \u003cp\u003eStork Enamine Reaction.\u003c\/p\u003e \u003cp\u003eStrecker Synthesis.\u003c\/p\u003e \u003cp\u003eSuzuki Reaction.\u003c\/p\u003e \u003cp\u003eSwern Oxidation.\u003c\/p\u003e \u003cp\u003eTiffeneau–Demjanov Reaction.\u003c\/p\u003e \u003cp\u003eVilsmeier Reaction.\u003c\/p\u003e \u003cp\u003eVinylcyclopropane Rearrangement.\u003c\/p\u003e \u003cp\u003eWagner–Meerwein Rearrangement.\u003c\/p\u003e \u003cp\u003eWeiss Reaction.\u003c\/p\u003e \u003cp\u003eWillgerodt Reaction.\u003c\/p\u003e \u003cp\u003eWilliamson Ether Synthesis.\u003c\/p\u003e \u003cp\u003eWittig Reaction.\u003c\/p\u003e \u003cp\u003eWittig Rearrangement.\u003c\/p\u003e \u003cp\u003eWohl–Ziegler Bromination.\u003c\/p\u003e \u003cp\u003eWolff Rearrangement.\u003c\/p\u003e \u003cp\u003eWolff–Kishner Reduction.\u003c\/p\u003e \u003cp\u003eWurtz Reaction.\u003c\/p\u003e \u003cp\u003eIndex.\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Chemistry [\u003ca title=\"See our other books on Chemistry\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Chemistry%20%5BPN%5D%22\"\u003ePN\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Interscience","offers":[{"title":"Brand New","offer_id":52474992427288,"sku":"9780470010419","price":47.99,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470010419.jpg?v=1785802699","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/named-organic-reactions-paperback-softback-9780470010419","provider":"Freshly Printed Books","version":"1.0","type":"link"}