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[null,"1.","Record Nr.",null,"UNINA9910457790103321"]
[null,null,"Autore",null,"Hassner Alfred"]
[null,null,"Titolo",null,"Organic syntheses based on name reactions [[electronic resource] ] : a practical guide to over 750 transformations / / A. Hassner, I. Namboothiri"]
[null,null,"Pubbl/distr/stampa",null,"Oxford, : Elsevier, 2012"]
[null,null,"ISBN",null,"1-283-34773-3"]
[{"$nulls":4},"9786613347732"]
[{"$nulls":4},"0-08-096631-4"]
[null,null,"Edizione",null,"[3rd ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (612 p.)"]
[null,null,"Disciplina",null,"547.2"]
[{"$nulls":4},"547/.2"]
[null,null,"Soggetti",null,"Organic compounds - Synthesis"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Includes indexes."]
[null,null,"Nota di contenuto",null,"Front 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"]
[{"$nulls":4},"ALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole Synthesis"]
[{"$nulls":4},"BAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN "]
[{"$nulls":4},"Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination Reagent"]
[{"$nulls":4},"BARTON 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"]
[{"$nulls":4},"BIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde Synthesis"]
[{"$nulls":4},"BOULTON-KATRITZKY Heterocyclic Rearrangement"]
[null,null,null,"Sommario/riassunto","Organic 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"]