LEADER 03898nam 2200613 a 450 001 9910820978603321 005 20230725025727.0 010 $a1-299-31411-2 010 $a0-470-87221-7 010 $a0-470-87220-9 035 $a(CKB)2670000000060446 035 $a(EBL)624414 035 $a(OCoLC)676969617 035 $a(SSID)ssj0000423721 035 $a(PQKBManifestationID)11281043 035 $a(PQKBTitleCode)TC0000423721 035 $a(PQKBWorkID)10458533 035 $a(PQKB)11213974 035 $a(MiAaPQ)EBC624414 035 $a(Au-PeEL)EBL624414 035 $a(CaPaEBR)ebr10469627 035 $a(CaONFJC)MIL462661 035 $a(EXLCZ)992670000000060446 100 $a20100311d2010 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 00$aName reactions for carbocyclic ring formations$b[electronic resource] /$fedited by Jie Jack Li ; foreword by E.J. Corey 210 $aHoboken, N.J. $cWiley$dc2010 215 $a1 online resource (774 p.) 225 1 $aWiley series on comprehensive name reactions 300 $aDescription based upon print version of record. 311 $a0-470-08506-1 320 $aIncludes bibliographical references and index. 327 $aName Reactions for Carbocyclic Ring Formations; Contents; Foreword; Preface; Contributing Authors; Chapter 1 Three-Membered Carbocycles; 1.1 Freund Reaction; 1.2 Kishner Cyclopropane Synthesis; 1.3 Kulinovich Cyclopropanol Synthesis; 1.4 Simmons-Smith Cyclopropanation; Chapter 2 Four-Membered Carbocycles; 2.1 Staudinger Ketene Cycloaddition; Chapter 3 Five-Membered Carbocycles; 3.1 Danheiser Annulation; 3.2 Dieckmann Condensation; 3.3 Favorskii Rearrangement; 3.4 Nazarov Cyclization; 3.5 Pauson-Khand Reaction; 3.6 Weiss-Cook Reaction; Chapter 4 Six-Membered Carbocycles 327 $a4.1 Bardhan-Sengupta Pheantherene Synthesis4.2 Bergman Cyclization; 4.3 Bogert-Cook Reaction; 4.4 Bradsher Cycloaddition and Bradsher Reaction; 4.5 Bradsher Reaction; 4.6 Darzens Synthesis of Tetralin Derivatives; 4.7 Diels-Alder Reaction; 4.8 Do?tz Benzannulation; 4.9 Elbs Reaction; 4.10 Fujimoto-Belleau Reaction; 4.11 Haworth Reaction; 4.12 Moore Cyclization; 4.13 Myers-Saito Cyclization; 4.14 Robinson Annulation; 4.15 Scholl Reaction; Chapter 5 Large-Ring Carbocycles; 5.1 Buchner Reaction; 5.2 de Mayo Reaction; 5.3 Ring-closing Metathesis (RCM); 5.4 Thorpe-Ziegler Reaction 327 $aChapter 6 Transformations of Carbocycles 6.1 Blanc Chloromethylation Reaction; 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present; 6.3 Houben-Hoesch Reaction; 6.4 Kolbe-Schmitt Reaction; 6.5 Vilsmeier-Haack Reaction; 6.6 von Richter Reaction; Appendices; 1, Contents Volume 1: Name Reactions in Heterocyclic Chemistry; 2, Contents Volume 2: Name Reactions for Functional Group Transformations; 3, Contents Volume 3: Name Reactions for Homologations-Part I; 4, Contents Volume 4: Name Reactions for Homologations-Part II; 5, Contents Volume 6: Name Reactions in Heterocyclic Chemistry-Part II 327 $aSubject Index 330 $aThis book continues the well-established and authoritative series on name reactions in organic chemistry by focusing on name reactions on ring formation. Ring formatting reactions have found widespread applicability in traditional organic synthesis, medicinal/pharmaceuticals, agricultural, fine chemicals, and of late, especially in polymer science. 410 0$aComprehensive name reactions. 606 $aRing formation (Chemistry) 615 0$aRing formation (Chemistry) 676 $a547/.2 701 $aLi$b Jie Jack$0440094 701 $aCorey$b E. J$020674 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910820978603321 996 $aName reactions for carbocyclic ring formations$94051159 997 $aUNINA