LEADER 05017nam 2200685Ia 450 001 9910676659203321 005 20201207144512.0 010 $a9786610344611 010 $a0-471-47381-2 010 $a1-280-34461-X 010 $a1-280-36693-1 010 $a9786610366934 010 $a0-470-35209-4 010 $a0-471-46155-5 010 $a0-471-21246-6 035 $a(CKB)1000000000018995 035 $a(EBL)175908 035 $a(OCoLC)808014229 035 $a(SSID)ssj0000168011 035 $a(PQKBManifestationID)11184167 035 $a(PQKBTitleCode)TC0000168011 035 $a(PQKBWorkID)10178835 035 $a(PQKB)10566659 035 $a(MiAaPQ)EBC175908 035 $a(MiAaPQ)EBC4471378 035 $a(PPN)159675774 035 $a(EXLCZ)991000000000018995 100 $a20020909d2002 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aHandbook of organopalladium chemistry for organic synthesis /$fedited by Ei-ichi Negishi 210 $aNew York $cWiley Interscience$dc2002 215 $a1 online resource (3279 p.) 300 $aDescription based upon print version of record. 311 $a0-471-31506-0 320 $aIncludes bibliographical references and index. 327 $aHANDBOOK OF ORGANOPALLADIUM CHEMISTRY FOR ORGANIC SYNTHESIS Volume 2; CONTENTS; PREFACE; CONTRIBUTORS; ABBREVIATIONS; V PALLADIUM-CATALYZED REACTIONS INVOLVING NUCLEOPHILIC ATTACK ON LIGANDS; V.1 Background for Part V; V.2 Palladium-Catalyzed Nucleophilic Substitution Involving Allylpalladium, Propargylpalladium, and Related Derivatives; V.2.1 The Tsuji-Trost Reaction and Related Carbon-Carbon Bond Formation Reactions; V.2.1.1 Overview of the Palladium-Catalyzed Carbon-Carbon Bond Formation via p-Allylpalladium and Propargylpalladium Intermediates 327 $aV.2.1.2 Synthetic Scope of the Tsuji-Trost Reaction with Allylic Halides, Carboxylates, Ethers, and Related Oxygen Nucleophiles as Starting CompoundsV.2.1.3 Palladium-Catalyzed Allylation with Allyl Carbonates; V.2.1.4 Palladium-Catalyzed Allylation and Related Substitution Reactions of Enolates and Related Derivatives of "Ordinary" Ketones, Aldehydes, and Other Carbonyl Compounds; V.2.1.5 Palladium-Catalyzed Substitution Reactions of Alkenyl Epoxides; V.2.1.6 Palladium-Catalyzed Substitution Reactions of Sulfur and Other Heavier Group 16 Atom-Containing Allylic Derivatives 327 $aV.2.1.7 Palladium-Catalyzed Substitution Reactions of Nitrogen and Other Group 15 Atom-Containing Allylic DerivativesV.2.1.8 Palladium-Catalyzed Substitution Reactions with Propargyl and Related Electrophiles; V.2.1.9 Palladium-Catalyzed Reactions of Soft Carbon Nucleophiles with Dienes, Vinylcyclopropanes, and Related Compounds; V.2.2 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Nitrogen, Oxygen, and Other Groups 15-17 Heteroatom Nucleophiles 327 $aV.2.2.1 Palladium-Catalyzed Substitution Reactions of Allylic, Propargylic, and Related Electrophiles with Heteroatom NucleophilesV.2.2.2 C-O and C-N Bond Formation Involving Conjugated Dienes and Allylpalladium Intermediates; V.2.2.3 Use of Alkenes as Precursors to p-Allylpalladium Derivatives in Allylic Substitution with O, N and Other Heteroatom Nucleophiles; V.2.3 Palladium-Catalyzed Allylic, Propargylic, and Allenic Substitution with Hydrogen and Metal Nucleophiles; V.2.3.1 Palladium-Catalyzed Hydrogenolysis of Allyl and Related Derivatives 327 $aV.2.3.2 Palladium-Catalyzed Deprotection of Allyl-Based Protecting GroupsV.2.3.3 Palladium-Catalyzed Allylic and Related Silylation and Other Metallations; V.2.3.4 Palladium-Catalyzed Reactions of Allyl and Related Derivatives with Organoelectrophiles; V.2.4 Palladium-Catalyzed Asymmetric Allylation and Related Reactions; V.2.5 Other Reactions of Allylpalladium and Related Derivatives; V.2.5.1 Elimination of Allylpalladium and Related Derivatives; V.2.5.2 Cycloaddition Reactions of Allylpalladium and Related Derivatives; V.2.5.3 Rearrangements of Allylpalladium and Related Derivatives 327 $aV.2.6 Synthesis of Natural Products and Biologically Active Compounds via Allylpalladium and Related Derivatives 330 $aOrganized to provide maximum utility to the bench synthetic chemist.The editor is well-known for his work in exploring, developing, and applying organopalladium chemistry.Contributors include over 24 world authorities in the field. 606 $aOrganic compounds$xSynthesis$vHandbooks, manuals, etc 606 $aPalladium catalysts$vHandbooks, manuals, etc 615 0$aOrganic compounds$xSynthesis 615 0$aPalladium catalysts 676 $a547.2 676 $a547/.2 701 $aNegishi$b Ei-ichi$092912 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910676659203321 996 $aHandbook of organopalladium chemistry for organic synthesis$93066462 997 $aUNINA