LEADER 05225nam 2200661Ia 450 001 9910144299003321 005 20170810192831.0 010 $a1-280-72267-3 010 $a9786610722679 010 $a3-527-60992-X 010 $a3-527-60868-0 035 $a(CKB)1000000000376476 035 $a(EBL)481326 035 $a(OCoLC)78204238 035 $a(SSID)ssj0000140879 035 $a(PQKBManifestationID)11148363 035 $a(PQKBTitleCode)TC0000140879 035 $a(PQKBWorkID)10054651 035 $a(PQKB)11155793 035 $a(PQKBManifestationID)16031353 035 $a(PQKB)20487317 035 $a(MiAaPQ)EBC481326 035 $a(EXLCZ)991000000000376476 100 $a19981007d2006 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aDomino reactions in organic synthesis$b[electronic resource] /$fLutz F. Tietze, Gordon Brasche, and Kersten M. Gericke 210 $aWeinheim $cWiley-VCH$dc2006 215 $a1 online resource (633 p.) 300 $aDescription based upon print version of record. 311 $a3-527-29060-5 320 $aIncludes bibliographical references and index. 327 $aDomino Reactions in Organic Synthesis; Table of Contents; Preface; Abbreviations; Introduction; Classification; 1 Cationic Domino Reactions; 1.1 Cationic/Cationic Processes; 1.1.1 Cationic/Cationic/Cationic Processes; 1.2 Cationic/Pericyclic Processes; 1.3 Cationic/Reductive Processes; 2 Anionic Domino Reactions; 2.1 Anionic/Anionic Processes; 2.1.1 Anionic/Anionic/Anionic Processes; 2.1.2 Fourfold and Higher Anionic Processes; 2.1.3 Two- and Threefold Anionic Processes Followed by a Nonanionic Process; 2.2 Anionic/Radical Processes; 2.3 Anionic/Pericyclic Processes 327 $a2.3.1 Anionic/Pericyclic Processes Followed by Further Transformations2.4 Anionic/Transition Metal-Catalyzed Processes; 2.5 Anionic/Oxidative or Reductive Processes; 3 Radical Domino Reactions; 3.1 Radical/Cationic Domino Processes; 3.2 Radical/Anionic Domino Processes; 3.3 Radical/Radical Domino Processes; 3.3.1 Radical/Radical/Anionic Domino Processes; 3.3.2 Radical/Radical/Radical Domino Processes; 3.3.3 Radical/Radical/Pericyclic Domino Processes; 3.3.4 Radical/Radical/Oxidation Domino Processes; 3.4 Radical/Pericyclic Domino Processes; 4 Pericyclic Domino Reactions 327 $a4.1 Diels-Alder Reactions4.1.1 Diels-Alder/Diels-Alder Reactions; 4.1.2 Diels-Alder Reactions/Sigmatropic Rearrangements; 4.1.3 Diels-Alder/Retro-Diels-Alder Reactions; 4.1.4 Diels-Alder Reactions/Mixed Transformations; 4.1.5 Hetero-Diels-Alder Reactions; 4.2 1,3-Dipolar Cycloadditions; 4.3 [2+2] and Higher Cycloadditions; 4.4 Sigmatropic Rearrangements; 4.5 Electrocyclic Reactions; 4.6 Ene Reactions; 4.7 Retro-Pericyclic Reactions; 5 Photochemically Induced Domino Processes; 5.1 Photochemical/Cationic Domino Processes; 5.2 Photochemical/Anionic Domino Processes 327 $a5.3 Photochemical/Radical Domino Processes5.4 Photochemical/Pericyclic Domino Processes; 5.5 Photochemical/Photochemical Domino Processes; 5.6 Photochemical/Transition Metal-Catalyzed Domino Processes; 6 Transition Metal-Catalyzed Domino Reactions; 6.1 Palladium-Catalyzed Transformations; 6.1.1 The Heck Reaction; 6.1.1.1 Domino Heck Reactions; 6.1.1.2 Heck/Cross-Coupling Reactions; 6.1.1.3 Heck/Tsuji-Trost Reactions; 6.1.1.4 Heck Reactions/CO-Insertions; 6.1.1.5 Heck Reactions/C-H-Activations; 6.1.1.6 Heck Reactions: Pericyclic Transformations; 6.1.1.7 Heck Reactions/Mixed Transformations 327 $a6.1.2 Cross-Coupling Reactions6.1.2.1 Suzuki Reactions; 6.1.2.2 Stille Reactions; 6.1.2.3 Sonogashira Reactions; 6.1.2.4 Other Cross-Coupling Reactions; 6.1.3 Nucleophilic Substitution (Tsuji-Trost Reaction); 6.1.4 Reactions of Alkynes and Allenes; 6.1.5 Other Pd(0)-Catalyzed Transformations; 6.1.6 Pd(II)-Catalyzed Transformations; 6.2 Rhodium-Catalyzed Transformations; 6.2.1 Formation of Carbenes; 6.2.2 Hydroformylations; 6.2.3 Other Rhodium-Catalyzed Transformations; 6.3 Ruthenium-Catalyzed Transformations; 6.3.1 Metathesis Reactions; 6.3.1.1 Metathesis-Metathesis Processes 327 $a6.3.1.2 Metathesis/Heck Reaction/Pericyclic Reaction/Hydrogenation 330 $aDomino reactions enable you to build complex structures in one-pot reactions without the need to isolate intermediates- a dream comes true. In this book, the well-respected expert, Professor Lutz Tietze, summarizes the possibilities of this reaction type - an approach for an efficiant, economically benificial and ecologicalbenign synthesis.A definite must for every organic chemist. 606 $aOrganic compounds$xSynthesis 606 $aChemical reactions 608 $aElectronic books. 615 0$aOrganic compounds$xSynthesis. 615 0$aChemical reactions. 676 $a547.1393 700 $aTietze$b Lutz-Friedjan$091380 701 $aBrasche$b Gordon$f1976-$0968007 701 $aGericke$b Kersten M.$f1976-$0968008 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910144299003321 996 $aDomino reactions in organic synthesis$92198462 997 $aUNINA LEADER 01328nam 2200253la 450 001 9910481708203321 005 20210618143006.0 035 $a(UK-CbPIL)2090299853 035 $a(CKB)5500000000107439 035 $a(EXLCZ)995500000000107439 100 $a20210618d1557 uy | 101 0 $aita 135 $aurcn||||a|bb| 200 13$aLa istoria di santo Antonino arciuescouo di Firenze. Nella qual si narra come per la sua santita fu creato arciuescouo di Firenze da papa Eugenio quarto, e di molti miracoli fece in uita e doppo morte qual mori adi 2 di maggio 1459 e fu sepolto in S. Marco di firenze [composta per frate Giouanmaria Tolosani dellordine de predicatori]$b[electronic resource] 210 $aItaly $c[s.n.]$d1557 215 $aOnline resource ([4] c., 4°) 300 $aReproduction of original in Biblioteca Nazionale Centrale di Firenze. 700 $aTolosani$b Giovanni Maria$f1472-1549.$0202538 801 0$bUk-CbPIL 801 1$bUk-CbPIL 906 $aBOOK 912 $a9910481708203321 996 $aLa istoria di santo Antonino arciuescouo di Firenze. Nella qual si narra come per la sua santita fu creato arciuescouo di Firenze da papa Eugenio quarto, e di molti miracoli fece in uita e doppo morte qual mori adi 2 di maggio 1459 e fu sepolto in S. Marco di firenze$92059418 997 $aUNINA