LEADER 05265nam 2200649 a 450 001 9910457790103321 005 20200520144314.0 010 $a1-283-34773-3 010 $a9786613347732 010 $a0-08-096631-4 035 $a(CKB)2550000000074522 035 $a(EBL)829958 035 $a(SSID)ssj0000592324 035 $a(PQKBManifestationID)12244226 035 $a(PQKBTitleCode)TC0000592324 035 $a(PQKBWorkID)10736184 035 $a(PQKB)11411100 035 $a(MiAaPQ)EBC829958 035 $a(PPN)182571424 035 $a(Au-PeEL)EBL829958 035 $a(CaPaEBR)ebr10518436 035 $a(CaONFJC)MIL334773 035 $a(OCoLC)769344338 035 $a(EXLCZ)992550000000074522 100 $a20111221d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aOrganic syntheses based on name reactions$b[electronic resource] $ea practical guide to over 750 transformations /$fA. Hassner, I. Namboothiri 205 $a3rd ed. 210 $aOxford $cElsevier$d2012 215 $a1 online resource (612 p.) 300 $aIncludes indexes. 311 $a0-08-096630-6 327 $aFront Cover; Organic Syntheses Basedon Name Reactions: A Practical Guide to 750 Transformations; Copyright; Contents; Foreword by D. Seebach; Foreword by S. Danishefsky; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; An Overview of Synthesis Related Name Reactions; Overview - Pd Catalyzed C-C Coupling Name Reactions; List of Abbreviations; ABIKO-MASAMUNE Asymmetric Aldol Reaction; ABRAMOV Asymmetric Phosphonylation; ACHMATOWICZ Furanylcarbinol Rearrangement; ACYLOIN Rearrangement; ADLER Phenol Oxidation; ALDER (Ene) Reaction 327 $aALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis 327 $aBAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent 327 $aBARTON ArylationBARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON-KELLOG Olefination; BARTON-McCOMBIE Alcohol Deoxygenation; BART-SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND-STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone Synthesis 327 $aBIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde Synthesis 327 $aBOULTON-KATRITZKY Heterocyclic Rearrangement 330 $aOrganic Syntheses Based on Named Reactions is an indispensable reference companion for chemistry students and researchers. Building on Hassner & Stumer's highly regarded 2e, this new work reviews 750 reactions, with over 100 new stereoselective and regioselective reactions. Each A-Z entry provides a carefully condensed summary of valuable information that a chemist needs to understand and utilize these fundamental reactions in their work, including brief practical details. The book is illustrated with real synthetic examples from the literature and about 3,400 references to the prima 606 $aOrganic compounds$xSynthesis 608 $aElectronic books. 615 0$aOrganic compounds$xSynthesis. 676 $a547.2 676 $a547/.2 700 $aHassner$b Alfred$092785 701 $aNamboothiri$b I$01034707 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910457790103321 996 $aOrganic syntheses based on name reactions$92454002 997 $aUNINA