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[null,"1.","Record Nr.",null,"UNINA9910144280503321"]
[null,null,"Titolo",null,"Modern acetylene chemistry / / edited by P. J. Stang and F. Diederich"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, [Germany] : , : VCH, , 1995"]
[{"$nulls":4},"©1995"]
[null,null,"ISBN",null,"1-281-84274-5"]
[{"$nulls":4},"9786611842741"]
[{"$nulls":4},"3-527-61527-X"]
[{"$nulls":4},"3-527-61526-1"]
[null,null,"Descrizione fisica",null,"1 online resource (530 p.)"]
[null,null,"Disciplina",null,"547.413"]
[null,null,"Soggetti",null,"Acetylene"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references at the end of each chapters and index."]
[null,null,"Nota di contenuto",null,"Modern Acetylene Chemistry; Contents; Foreword; List of Contributors; 1 Modern Computational and Theoretical Aspects of Acetylene Chemist; 1.1 Introduction; 1.2 Electronic structures of acetylene and monoacetylenes; 1.2.1 Ground-state potential energy surfaces; 1.2.2 Excited-state potential energy surfaces; 1.2.3 Radical Ions; 1.3 Reactivities and molecular interactions of acetylenes; 1.3.1 Pericyclic reactions; 1.3.2 Electrophilic reactions; 1.3.3 Nucleophilic additions; 1.3.4 Radical additions; 1.3.5 Molecular complexes; 1.4 Polyacetylenes; 1.4.1 Diacetylene; 1.4.2 Cn and cyclic Cn"]
[{"$nulls":4},"1.4.2.1 C21.4.2.2 C3; 1.4.2.3 C4; 1.4.2.4 C5, C7, and C9; 1.4.2.5 C6, C8 and C10; 1.4.2.6 C11 to C17; 1.4.2.7 C18; 1.5 Conclusion; References; 2 Functionalized Acetylenes in Organic Synthesis - The Case of the 1-Cyano- and the 1-Halogenoacetylenes; 2.1 Introduction; 2.2 Synthesis and preparative use of cyanoacetylenes; 2.2.1 Synthesis; 2.2.2 Preparative use of cyanoacetylenes; 2.2.2.1 A short summary of the older literature; 2.2.2.2 Novel cycloadditions with cyanoacetylenes - simple and efficient methods for the construction of complex carbon frame"]
[{"$nulls":4},"2.2.2.3 Cyanoacetylenes as precursors for reactive and interstellar intermediates2.3 Synthesis and preparative use of 1-halogenoacetylenes; 2.3.1 Older review of the literature on "]
[{"$nulls":4},"halogenoacetylenes; 2.3.2 Synthesis of 1-halogenoacetylenes; 2.3.2.1 The preparation of the 1-Halogeno- and 1,2-Dihalogenoethynes; 2.3.2.2 More highly unsaturated halogenoacetylenes; 2.3.2.3 Derivatives of 1-halogenoacetylenes; 2.3.3 Novel preparative uses of 1-Halogeno- and 1,2-Dihalogenoacetylenes; 2.4 Experimental procedures; 2.4.1 Cyanoacetylene (1); 2.4.2 Dicyanoacetylene (2); 2.4.3 Dicyanodiacetylene (3)"]
[{"$nulls":4},"2.4.4 Chloroacetylene (93)2.4.5 Dichloroacetylene (100); 2.4.6 Diiodoacetylene (105); References; 3 Alkynyliodonium Salts: Electrophilic Acetylene Equivalents; 3.1 Introduction; 3.2 Preparation and properties; 3.2.1 Alkynyliodonium sulfonates; 3.2.2 Alkynyliodonium tetrafluoroborates; 3.2.3 Heterocyclic alkynyliodonium species; 3.2.4 Mechanism of formation; 3.2.5 Diynyliodonium and dialkynyliodonium triflates; 3.2.6 Bis-iodonium species; 3.2.7 Properties of alkynyliodonium salts; 3.3 Characterization and structure; 3.3.1 Spectroscopic properties; 3.3.2 X-ray and molecular structure"]
[{"$nulls":4},"3.4 Reactions and uses of alkynyliodonium salts3.4.1 Reaction with nucleophiles; 3.4.1.1 Carbon nucleophiles; 3.4.1.2 Nitrogen nucleophiles; 3.4.1.3 Oxygen nucleophiles; 3.4.1.4 Sulfur nucleophiles; 3.4.1.5 Phosphorus nucleophiles; 3.4.1.6 Halogen nucleophiles; 3.4.2 Reaction with organometallic species; 3.4.3 Cycloaddition reactions; 3.4.3.1 [2 + 4]-Diels-Alder cycloadditions; 3.4.3.2 1,3-Dipolar cycloadditions; 3.5 Conclusions; 3.6 Experimental procedures; 3.6.1 (Cyano{[(trifluoromethyl)sulfonyl]oxy)iodo}benzene, 7"]
[{"$nulls":4},"3.6.2 General procedure for the preparation of β-alkyl- and β-phenylethynyl(phenyl)iodonium triflates, 10"]
[null,null,null,"Sommario/riassunto","This comprehensive handbook presents the full potential of modern acetylene chemistry, from organic synthesis through materials science to bioorganic chemistry.K. Houk, H. Hopf, P. Stang, K. M. Nicholas, N. Schore, M. Regitz, K. C. Nicolaou, R. Gleiter, L. Scott, R. Grubbs, H. Iwamura, J. Moore, and F. Diederich - internationally renowned authors introduce the reader, in a didactically skilful manner, to the state-of-the-art in alkyne chemistry. Emphasis is placed on presenting carefully selected and instructive examples as well as essential references to the original literature.<b"]