LEADER 05406nam 2200661Ia 450 001 9910784534503321 005 20200520144314.0 010 $a1-281-74939-7 010 $a9786611749392 010 $a0-08-053314-0 035 $a(CKB)1000000000384414 035 $a(EBL)404411 035 $a(OCoLC)476218369 035 $a(SSID)ssj0000168019 035 $a(PQKBManifestationID)11161507 035 $a(PQKBTitleCode)TC0000168019 035 $a(PQKBWorkID)10178216 035 $a(PQKB)10437274 035 $a(MiAaPQ)EBC404411 035 $a(Au-PeEL)EBL404411 035 $a(CaPaEBR)ebr10243850 035 $a(CaONFJC)MIL174939 035 $a(PPN)182569047 035 $a(EXLCZ)991000000000384414 100 $a19970415d1997 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aHandbook of palladium-catalyzed organic reactions$b[electronic resource] $esynthetic aspects and catalytic cycles /$fJ.-L. Malleron, J.-C. Fiaud and J.-Y. Legros 210 $aSan Diego $cAcademic Press$dc1997 215 $a1 online resource (319 p.) 300 $aDescription based upon print version of record. 311 $a0-12-466615-9 327 $aFront Cover; Handbook of Palladium-Catalyzed Organic Reactions: Synthetic Aspects and Catalytic Cycles; Copyright Page; Table of Contents; Foreword; Abbreviations; I- Introduction; II- Graphical abstracts of reaction numbers (RXN); III- Reactions catalysed by palladium complexes; RXN1 Cross-Coupling of Organometallics with RX Derivatives; RXN2 Cross-Coupling of Organometallics with RCOX Derivatives; RXN3 Cross-Coupling of Siloxycyclopropanes with RX and RCOX Derivatives; RXN4 Cross-Coupling of Terminal Alkynes with RX Derivatives; RXN5 Intermolecular HECK Reaction 327 $aRXN6 Intramolecular HECK ReactionRXN7 Intramolecular Coupling of Di(Vinyl Halides); RXN8 Tandem HECK-Anion Capture Process of Alkenes, Alkynes, Allenes and Dienes; RXN9 Tandem HECK-Anion Capture Process of Norbornene and Related Compounds; RXN10 Tandem Arylsulfonation-Cyclization Process; RXN11 Tandem Cyclization-Anion Capture (-Carbonylation) Process of Alkenes, Allenes and Alkynes; RXN12 Tandem Cyclization-Anion-Capture Process of Ene-Vinyl, Ene-Aryl and Ene-Alkyl Halides; RXN13 Tandem Cyclization-Anion Capture (-Carbonylation) Process of Yne-Vinyl and Yne-Aryl Halides 327 $aRXN14 Hydroarylation and Hydrovinylation of Alkenes and AlkynesRXN15 Reduction of Alkenes; RXN16 Semihydrogenation of Alkynes and 1,3-Dienes; RXN17 Hydroboration, Hydrogermylation, Hydrosilylation and Hydrostannation of Alkynes, Allenes, Dienes and Enynes; RXN18 Hydroselenation of Alkynes; RXN19 1,4- Disilylation of Conjugated Enones; RXN20 Hydrocarboxylation, Hydrocarboalkoxylation and Hydrocarboamination of Alkenes and Alkynes; RXN21 Tandem Carbonylation-Arylation with Alkynes; RXN22 1,2-Dimetallation of Alkynes and Alkenes and Related Reactions; RXN23 1,2-Dimetallation of Isonitriles 327 $aRXN24 1,2-Dimetallation of Allenes or 1,3-DienesRXN25 Coupling of Aryl Derivatives with Alkenes Involving a Pd(II) Catalyst; RXN26 Homocoupling of Aryl and Vinyl Derivatives; RXN27 Codimerization of Alkynes; RXN28 Codimerization of Terminal Alkynes with Allenes; RXN29 Codimerization of Alkynes and Allyl Halides; RXN30 Cyclopropanation of Alkenes and 1,3-Dienes by Diazomethane; RXN31 Rearrangement of ?-Hydroxy Diazo Compounds; RXN32 Substitution, Addition and Elimination on Pro-?-Allyl Substrates; RXN33 [3,3]-Sigmatropic Rearrangement and [1,3]-Shift on Allylic Derivatives 327 $aRXN34 1,3-Diene Monoepoxide RearrangementRXN35 Ring Extension of Cyclobutane Derivatives; RXN36 [3+2], [3+4], [3+6], [1+2] Cycloadditions; RXN37 Intramolecular Ene-Like Reactions; RXN38 Cyclization of Hexatrienolate Derivatives; RXN39 Amination or Amidation of Alkenes; RXN40 Alkoxylation of Alkenes and Alkynes; RXN41 Acetalization of Alkenes; RXN42 Allylic Acyloxylation of Cycloalkenes; RXN43 Tandem Acyloxylation-Cyclization of 1,5-Dienes; RXN44 Tandem Acyloxychlorination-Cyclization of 1,6-Dienes; RXN45 1,4-Acyloxychlorination of 1,3-Dienes 327 $aRXN46 1,4-Diacyloxylation of 1,3-Dienes and Related Reactions 330 $aThis comprehensive handbook will be an indispensable research tool for chemists. Handbook of Palladium Catalysed Organic Reactions provides a synoptic description of the main types of reactions which are catalyzed by Palladium and the mechanism which causes these reactions. Each reaction is presented in graphical form and classified according to the type of transformation involved.Other books covering the use of Palladium complexes as catalysts have been written, but the Handbook is the only to offer a synoptic view, showing the catalytic cycle of each reaction. This complete 606 $aChemistry, Inorganic 606 $aPalladium catalysts 615 0$aChemistry, Inorganic. 615 0$aPalladium catalysts. 676 $a547.1395 700 $aMalleron$b Jean-Luc$0747161 701 $aFiaud$b J. C$01500578 701 $aLegros$b J.-Y$g(Jean-Yves)$01500579 701 $aMalleron$b Jean-Luc$0747161 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910784534503321 996 $aHandbook of palladium-catalyzed organic reactions$93727316 997 $aUNINA