LEADER 01710nam 2200397Ia 450 001 996395677303316 005 20221107143417.0 035 $a(CKB)3810000000015755 035 $a(EEBO)2240900636 035 $a(OCoLC)316340105 035 $a(EXLCZ)993810000000015755 100 $a20090319d1553 uy 0 101 0 $aeng 135 $aurbn||||a|bb| 200 10$aCommo[n] places of scripture$b[electronic resource] $eordrely and after a compendious forme of teaching, set forth with no litle laboure, to y[e] great profit & help of all suche studentes in Gods word as haue not had longe exercise in the same, /$fby the right excellent clerke Eras. Sarcerius ; translated in to Englysh by Rychard Tauerner. 210 $aJmprynted at London $cby Nycolas Hyll, dwellynge in Sayncte Johns Strete.$dAnno Domini. M.D.LIII. [1553] 215 $a[14], clxv [i.e. 336], [2] p 300 $aTranslation of: Loci aliquot communes et theologici.--Cf. NUC pre-1956 imprints. 300 $aImprint from colophon. 300 $aSignatures: A-Y⁸. 300 $aPages numbered on recto only. 300 $aNumerous errors in paging. 300 $aTitle in ornamental border (McK. & F. 33); initials. 300 $aReproduction of original in: New York Public Library. 320 $aIncludes bibliographical references in marginal notes. 330 $aeebo-0103 606 $aTheology, Doctrinal 615 0$aTheology, Doctrinal. 700 $aSarcerius$b Erasmus$f1501-1559.$01003029 701 $aTaverner$b Richard$f1505?-1575.$01002663 801 0$bUMI 801 1$bUMI 906 $aBOOK 912 $a996395677303316 996 $aCommo places of scripture$92302630 997 $aUNISA LEADER 05308nam 2200709Ia 450 001 9911019428603321 005 20200520144314.0 010 $a9786610722679 010 $a9781280722677 010 $a1280722673 010 $a9783527609925 010 $a352760992X 010 $a9783527608683 010 $a3527608680 035 $a(CKB)1000000000376476 035 $a(EBL)481326 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(OCoLC)86225007 035 $a(Perlego)2758138 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 /$fLutz F. Tietze, Gordon Brasche, and Kersten M. Gericke 210 $aWeinheim $cWiley-VCH$dc2006 215 $a1 online resource (633 p.) 300 $aDescription based upon print version of record. 311 08$a9783527290604 311 08$a3527290605 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 $aChemical reactions 615 0$aOrganic compounds$xSynthesis. 615 0$aChemical reactions. 676 $a547.1393 700 $aTietze$b Lutz-Friedjan$091380 701 $aBrasche$b Gordon$f1976-$01838709 701 $aGericke$b Kersten M.$f1976-$01838710 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019428603321 996 $aDomino reactions in organic synthesis$94417757 997 $aUNINA