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[null,"1.","Record Nr.",null,"UNINA9910144276703321"]
[null,null,"Titolo",null,"Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008"]
[{"$nulls":4},"©2008"]
[null,null,"ISBN",null,"1-282-78423-4"]
[{"$nulls":4},"9786612784231"]
[{"$nulls":4},"3-527-62126-1"]
[{"$nulls":4},"3-527-62127-X"]
[null,null,"Descrizione fisica",null,"1 online resource (410 p.)"]
[null,null,"Classificazione",null,"35.62"]
[null,null,"Disciplina",null,"547.042"]
[{"$nulls":4},"572/.65"]
[null,null,"Soggetti",null,"Amino acids"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Tedesco"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references at the end of each chapters and index."]
[null,null,"Nota di contenuto",null,"Amino Group Chemistry; Contents; Preface; List of Contributors; 1 Simple Molecules, Highly Efficient Amination; 1.1 Introduction; 1.2 Hydroxylamine Derivatives; 1.2.1 O-Sulfonylhydroxylamine; 1.2.2 O-Phosphinylhydroxylamine; 1.2.3 O-Acylhydroxylamine; 1.2.4 O-Trimethylsilylhydroxylamine; 1.2.5 Experimental Procedures; 1.3 Oxime Derivatives; 1.3.1 Synthesis of Primary Amines by Electrophilic Amination of Carbanions; 1.3.2 Experimental Procedures; 1.4 Azo Compounds; 1.4.1 Azodicarboxylates; 1.4.1.1 Allylic Amination through Ene-Type Reactions; 1.4.1.2 Hydrohydrazination of Alkenes"]
[{"$nulls":4},"1.4.2 Arylazo Sulfones1.4.3 Experimental Procedures; 1.5 Oxaziridine Derivatives; 1.5.1 Electrophilic Amination of Carbon Nucleophiles; 1.5.2 Amination of Allylic and Propargylic Sulfides by Use of a Ketomalonate-Derived Oxaziridine; 1.5.3 Experimental Procedures; 1.6 Chloramine-T; 1.6.1 Aminochalcogenation of Alkenes; 1.6.2 Aminohydroxylation of Alkenes; 1.6.3 Aziridination of Alkenes; 1.6.4 Other Applications; 1.6.5 Experimental Procedures; 1.7 N-Sulfonyliminophenyliodinane; 1.7.1 Transition Metal-Catalyzed Amination of Alkenes; 1.7.2 Experimental Procedures"]
[{"$nulls":4},"1.8 Transition Metal-Nitride Complexes1.8.1 Nitrogen Atom Transfer "]
[{"$nulls":4},"Mediated by Transition Metal/Nitride Complexes; 1.8.2 Experimental Procedures; 1.9 Azido Derivatives; 1.9.1 Electrophilic Amination of Organometallic Reagents with Organic Azides; 1.9.2 Radical-Mediated Amination with Sulfonyl Azides; 1.9.3 Hydroazidation of Alkenes with Sulfonyl Azides; 1.9.4 Experimental Procedures; 1.10 Gabriel-Type Reagents; 1.10.1 Nucleophilic Amination Reactions; 1.10.2 Experimental Procedure; 1.11 Conclusion; 2 Catalytic C-H Amination with Nitrenes; 2.1 Introduction; 2.2 Historical Overview"]
[{"$nulls":4},"2.3 Hypervalent Iodine-Mediated C-H Amination2.3.1 Intramolecular C-H Amination; 2.3.1.1 From NH(2) Carbamates; 2.3.1.2 From NH(2) Sulfamates; 2.3.1.3 From Other Nitrogen Functionalities; 2.3.2 Intermolecular C-H Amination; 2.3.2.1 General Scope and Limitations; 2.3.2.2 Recent Major Improvements; 2.4 Other Nitrene Precursors for C-H Amination; 2.4.1 Azides; 2.4.2 Haloamines; 2.4.3 Carbamate Derivatives; 2.5 Amination of Aromatic C-H Bonds; 2.6 Applications in Total Synthesis; 2.6.1 Application of Intramolecular C-H Amination with Carbamates"]
[{"$nulls":4},"2.6.2 Application of Intramolecular C-H Amination with Sulfamates2.6.3 Application of Intermolecular C-H Amination; 2.7 Conclusions; 3 Nitroalkenes as Amination Tools; 3.1 Introduction; 3.2 General Strategies for the Synthesis of Nitroalkenes; 3.3 Synthesis of Alkylamines; 3.3.1 Monoamines; 3.3.2 Amino Acid Derivatives; 3.3.3 Amino Alcohols; 3.3.4 Diamino Derivatives; 3.4 Pyrrolidine Derivatives; 3.4.1 Pyrrolidinones; 3.4.2 Pyrrolidines; 3.5 Piperidines and Piperazines; 3.6 Pyrrolizidines and Related Derivatives; 3.7 Arene-Fused Nitrogen Heterocycles; 3.7.1 Pyrroloindole Derivatives"]
[{"$nulls":4},"3.7.2 Carbolines and their Tryptamine Precursors"]
[null,null,null,"Sommario/riassunto","Here, probably the most important functional group in organic chemistry is discussed in one handy volume. The monograph covers its application  -- from natural products to synthetic pharmaceuticals -- detailing complex syntheses using the amino group as templates and modern techniques focussing on the introduction of the amino group. A definitive must-have for every chemist."]
[null,"2.","Record Nr.",null,"UNINA9910812533703321"]
[null,null,"Autore",null,"Coquet Bruno"]
[null,null,"Titolo",null,"L'assurance chômage : une politique malmenée / / Bruno Coquet"]
[null,null,"Pubbl/distr/stampa",null,"Paris : , : L'Harmattan, , [2013]"]
[{"$nulls":4},"©2013"]
[null,null,"ISBN",null,"2-336-68023-8"]
[null,null,"Descrizione fisica",null,"1 online resource (227 pages ) : illustrations ;"]
[null,null,"Collana",null,"Collection Questions contemporaines"]
[null,null,"Disciplina",null,"368.44"]
[null,null,"Soggetti",null,"Unemployment insurance - Government policy - Europe"]
[null,null,"Lingua di pubblicazione",null,"Francese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Bibliographic Level Mode of Issuance: Monograph"]
[null,null,null,"Nota di bibliografia","Includes bibliographical references (pages 209-224)."]
[null,null,null,"Sommario/riassunto","L'assurance chômage est souvent réduite aux jugements définitifs qui sont portés sur elle : une charge, trop généreuse ou pas assez, compliquée, inefficace... Mais avant d'être une politique économique et sociale, l'assurance chômage est d'abord un produit d'assurance qui doit rendre le service que l'on attend, à un prix acceptable. Ainsi, un régime d'assurance chômage subtilement manié est en réalité un outil puissant, qui protège les individus et soutient les entreprises et la croissance."]