{"product_id":"name-reactions-for-carbocyclic-ring-formations-hardback-9780470085066","title":"Name Reactions for Carbocyclic Ring Formations (Hardback) 9780470085066","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eName Reactions for Carbocyclic Ring Formations\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\"\u003eJie Jack Li (Edited by), JJ Li (Author), E. J. Corey (Foreword by)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9780470085066, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 22 October 2010\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e772 pages\u003cbr\u003e24.3 x 19.8 x 4.3 cm, 1.474 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\"This comprehensive reference guide offers information on the most current developments in name reactions on carbocyclic ring formations, and is intended as a resource for both students and professionals working in organic chemistry and polymer synthesis.\" (Booknews, 1 February 2011)\u003c\/font\u003e\u003c\/em\u003e\u003c\/p\u003e\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eThis book continues the well-established and authoritative series on name reactions in organic chemistry by focusing on name reactions on ring formation.  Ring formating reactions have found widespread applicability in traditional organic synthesis, medicinal\/pharmaceuticals, agricultural, fine chemicals, and of late, especially in polymer science. \u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eForeword.  \u003cp\u003ePreface.\u003c\/p\u003e \u003cp\u003eContributing Authors.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 1 Three-Membered Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1.1 Freund Reaction.\u003c\/p\u003e \u003cp\u003e1.2 Kishner Cyclopropane Synthesis.\u003c\/p\u003e \u003cp\u003e1.3 Kulinovich Cyclopropanol Synthesis.\u003c\/p\u003e \u003cp\u003e1.4 Simmons-Smith Reaction.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 2 Four-Membered Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e2.1 Staudinger Ketene Cycloaddition.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 3 Five-Membered Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3.1 Danheiser Annulation.\u003c\/p\u003e \u003cp\u003e3.2 Dieckmann Condensation.\u003c\/p\u003e \u003cp\u003e3.3 Favorskii Rearrangement.\u003c\/p\u003e \u003cp\u003e3.4 Nazarov Cyclization.\u003c\/p\u003e \u003cp\u003e3.5 Pauson-Khand Reaction.\u003c\/p\u003e \u003cp\u003e3.6 Weiss–Cook Reaction.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 4 Six-Membered Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4.1 Bardhan-Sengupta Pheantherene Synthesis.\u003c\/p\u003e \u003cp\u003e4.2 Bergman Cyclization.\u003c\/p\u003e \u003cp\u003e4.3 Bogert-Cook Reaction.\u003c\/p\u003e \u003cp\u003e4.4 Bradsher Cycloaddition and Bradsher Reaction.\u003c\/p\u003e \u003cp\u003e4.5 Bradsher Reaction.\u003c\/p\u003e \u003cp\u003e4.6 Darzens Synthesis of Tetralin Derivatives.\u003c\/p\u003e \u003cp\u003e4.7 Diels-Alder Reaction.\u003c\/p\u003e \u003cp\u003e4.8 Dötz Benzannulation.\u003c\/p\u003e \u003cp\u003e4.9 Elbs Reaction.\u003c\/p\u003e \u003cp\u003e4.10 Fujimoto-Belleau Reaction.\u003c\/p\u003e \u003cp\u003e4.11 Haworth Reaction.\u003c\/p\u003e \u003cp\u003e4.12 Moore Cyclization.\u003c\/p\u003e \u003cp\u003e4.13 Myers-Saito Cyclization.\u003c\/p\u003e \u003cp\u003e4.14 Robinson Annulation.\u003c\/p\u003e \u003cp\u003e4.15 Scholl Reaction.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 5 Large-Ring Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5.1 Buchner Reaction.\u003c\/p\u003e \u003cp\u003e5.2 de Mayo Reaction.\u003c\/p\u003e \u003cp\u003e5.3 Ring-closing Metathesis (RCM).\u003c\/p\u003e \u003cp\u003e5.4 Thorpe-Ziegler Reaction.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eChapter 6 Transformations of Carbocycles.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e6.1 Blanc Chloromethylation Reaction.\u003c\/p\u003e \u003cp\u003e6.2 Asymmetric Friedel-Crafts Reactions: Past to Present.\u003c\/p\u003e \u003cp\u003e6.3 Houben-Hoesch Reaction.\u003c\/p\u003e \u003cp\u003e6.4 Kolbe-Schmitt Reaction.\u003c\/p\u003e \u003cp\u003e6.5 Vilsmeier-Haack Reaction.\u003c\/p\u003e \u003cp\u003e6.6 von Richter Reaction.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAppendices.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 Contents Volume 1: \u003ci\u003eName Reactions in Heterocyclic Chemistry\u003c\/i\u003e.\u003c\/p\u003e \u003cp\u003e2 Contents Volume 2: \u003ci\u003eName Reactions for Functional Group Transformations\u003c\/i\u003e.\u003c\/p\u003e \u003cp\u003e3 Contents Volume 3: \u003ci\u003eName Reactions for Homologations—Part I\u003c\/i\u003e.\u003c\/p\u003e \u003cp\u003e4 Contents Volume 4: \u003ci\u003eName Reactions for Homologations—Part II\u003c\/i\u003e.\u003c\/p\u003e \u003cp\u003e5 Contents Volume 6: \u003ci\u003eName Reactions in Heterocyclic Chemistry—Part II\u003c\/i\u003e.\u003c\/p\u003e \u003cp\u003eSubject Index.\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","offers":[{"title":"Brand New","offer_id":52257032962328,"sku":"9780470085066","price":138.56,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9780470085066.jpg?v=1781275915","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/name-reactions-for-carbocyclic-ring-formations-hardback-9780470085066","provider":"Freshly Printed Books","version":"1.0","type":"link"}