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[null,"1.","Record Nr.",null,"UNISALENTO991003289779707536"]
[null,null,"Autore",null,"Due Sicilie <Regno>"]
[null,null,"Titolo",null,"Collezione delle leggi e de' decreti reali del Regno delle Due Sicilie. Anno 1829. Semestre I. Da gennaio a tutto giugno"]
[null,null,"Pubbl/distr/stampa",null,"Napoli : dalla Stamperia Reale, 1829"]
[null,null,"Descrizione fisica",null,"xlii, 152 p., xv ; 20 cm"]
[null,null,"Disciplina",null,"340.457945.7"]
[null,null,"Soggetti",null,"Leggi e decreti - Raccolta - Regno delle Due Sicilie"]
[{"$nulls":4},"Regno delle Due Sicilie 1829 Legislazione"]
[null,null,"Lingua di pubblicazione",null,"Italiano"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,"2.","Record Nr.",null,"UNINA9910831093303321"]
[null,null,"Autore",null,"Ulrich Henri <1925->"]
[null,null,"Titolo",null,"Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich"]
[null,null,"Pubbl/distr/stampa",null,"Hoboken, NJ, : Wiley, 2009"]
[null,null,"ISBN",null,"1-282-46107-9"]
[{"$nulls":4},"9786612461071"]
[{"$nulls":4},"0-470-74795-1"]
[{"$nulls":4},"0-470-74793-5"]
[null,null,"Descrizione fisica",null,"1 online resource (566 p.)"]
[null,null,"Disciplina",null,"547.2"]
[{"$nulls":4},"547.412"]
[null,null,"Soggetti",null,"Alkenes"]
[{"$nulls":4},"Chemical reactions"]
[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","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Cumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions"]
[{"$nulls":4},"3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition Reactions"]
[{"$nulls":4},"References4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization "]
[{"$nulls":4},"Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References"]
[{"$nulls":4},"5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR2"]
[{"$nulls":4},"6.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O"]
[{"$nulls":4},"7.3.3 Sulfur Trioxide, O SO2"]
[null,null,null,"Sommario/riassunto","Cumulenes are organic molecules with two or more cumulative (consecutive) double bonds. Their reactions often proceed at room temperature, with or without a catalyst, and are stereospecific, giving the reaction products in high yields - features characteristic of \"click reactions\".   Cumulenes in Click Reactions presents a comprehensive list of cumulene systems and their reactions, with an emphasis on their \"click-like\" nature. The chapters are structured according to the number of carbon atoms in the system, including coverage of: introduction to the chemist"]