{"product_id":"name-reactions-for-carbocyclic-ring-formations-isbn-9780470085066","title":"Name Reactions for Carbocyclic Ring Formations","description":"This 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.   Foreword.  \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 \"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) \u003cb\u003eJIE JACK LI\u003c\/b\u003e is a chemist at Bristol-Myers Squibb Company in Wallingford, Connecticut. He has authored or edited various books, including \u003ci\u003eName Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Name Reactions for Homologations, Parts I and II, Contemporary Drug Synthesis, The Art of Drug Synthesis,\u003c\/i\u003e and \u003ci\u003eModern Drug Synthesis,\u003c\/i\u003e all published by Wiley.  “A valuable additon to the literature by any measure and surely will prove its merit in years to come. The new knowledge that arises with its help will be impressive and of great benefit to humankind.”\u003cbr\u003e —From the Foreword by \u003cb\u003eE.J. Corey,\u003c\/b\u003e Nobel laureate  \u003cp\u003e\u003cb\u003eAn invaluable guide to name reactions on carbocyclic ring formations\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eRing-forming reactions have found widespread applicability advantageous to the interests of science. Currently, they are used in all areas of organic synthesis, including medicinal and pharmaceutical, agricultural, fine chemicals, and, most recently, polymer science.\u003c\/p\u003e \u003cp\u003eThis all-inclusive reference focuses on name reactions specific to ring formations, and details the carbocyclic characteristics that make these rings an effective tool in the synthetic arsenal of organic chemistry with:\u003c\/p\u003e \u003cul\u003e \u003cli\u003e \u003cp\u003eA description of a ring-forming reaction included in each section highlighting the following: historical perspective, a mechanism for the reaction, variations and improvements on the reaction, synthetic utilities of the reaction, experimental details, and current references\u003c\/p\u003e \u003c\/li\u003e \u003cli\u003e \u003cp\u003eCoverage of fundamental topics, including various carbocycles (three, five, six, and large-ring carbocycles) and the transformation of carbocycles\u003c\/p\u003e \u003c\/li\u003e \u003cli\u003e \u003cp\u003eExamples of common name reactions, such as Simmons-Smith, Pauson-Khand, Danheiser annulation, Diels-Alder, Robinson annulation, Stork enamine reaction, and ring-closing metathesis\u003c\/p\u003e \u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003eAn excellent resource for both students and professionals involved with organic chemistry and polymer synthesis, \u003ci\u003eName Reactions for Carbocyclic Ring Formations\u003c\/i\u003e delivers essential information on the latest developments from leading experts in the field—and serves as a springboard to further advance scientific discovery.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47989668282597,"sku":"NP9780470085066","price":203.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9780470085066.jpg?v=1761785030","url":"https:\/\/k12savings.com\/products\/name-reactions-for-carbocyclic-ring-formations-isbn-9780470085066","provider":"K12savings","version":"1.0","type":"link"}