05017nam 2200685Ia 450 991067665920332120201207144512.097866103446110-471-47381-21-280-34461-X1-280-36693-197866103669340-470-35209-40-471-46155-50-471-21246-6(CKB)1000000000018995(EBL)175908(OCoLC)808014229(SSID)ssj0000168011(PQKBManifestationID)11184167(PQKBTitleCode)TC0000168011(PQKBWorkID)10178835(PQKB)10566659(MiAaPQ)EBC175908(MiAaPQ)EBC4471378(PPN)159675774(EXLCZ)99100000000001899520020909d2002 uy 0engur|n|---|||||txtccrHandbook of organopalladium chemistry for organic synthesis /edited by Ei-ichi NegishiNew York Wiley Intersciencec20021 online resource (3279 p.)Description based upon print version of record.0-471-31506-0 Includes bibliographical references and index.HANDBOOK 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 IntermediatesV.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 DerivativesV.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 NucleophilesV.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 DerivativesV.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 DerivativesV.2.6 Synthesis of Natural Products and Biologically Active Compounds via Allylpalladium and Related DerivativesOrganized 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.Organic compoundsSynthesisHandbooks, manuals, etcPalladium catalystsHandbooks, manuals, etcOrganic compoundsSynthesisPalladium catalysts547.2547/.2Negishi Ei-ichi92912MiAaPQMiAaPQMiAaPQBOOK9910676659203321Handbook of organopalladium chemistry for organic synthesis3066462UNINA