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Biblioteca

MARC Lista (tabellare)
Alkenes : recent advances, new perspectives and applications / / edited by Reza Davarnejad
Alkenes : recent advances, new perspectives and applications / / edited by Reza Davarnejad
Pubbl/distr/stampa London, England : , : IntechOpen, , [2021]
Descrizione fisica 1 online resource (130 pages) : illustrations
Disciplina 547.412
Soggetto topico Alkenes
ISBN 1-83969-536-6
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Alkenes
Record Nr. UNINA-9910586675503321
London, England : , : IntechOpen, , [2021]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkenes / / edited by Reza Davarnejad, Baharak Sajjadi
Alkenes / / edited by Reza Davarnejad, Baharak Sajjadi
Pubbl/distr/stampa London, England : , : InTech, , 2021
Descrizione fisica 1 online resource (180 pages)
Disciplina 547.412
Soggetto topico Alkenes
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Altri titoli varianti Alkenes
Record Nr. UNINA-9910688222403321
London, England : , : InTech, , 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkenes / / edited by Reza Davarnejad, Baharak Sajjadi
Alkenes / / edited by Reza Davarnejad, Baharak Sajjadi
Pubbl/distr/stampa Rijeka, Croatia : , : IntechOpen, , [2018]
Descrizione fisica 1 online resource (180 pages) : illustrations
Disciplina 547.412
Soggetto topico Alkenes
ISBN 953-51-3982-7
953-51-3767-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910265151303321
Rijeka, Croatia : , : IntechOpen, , [2018]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkenes and aromatics [[electronic resource] /] / edited by Peter Taylor [and Michael Gagan]
Alkenes and aromatics [[electronic resource] /] / edited by Peter Taylor [and Michael Gagan]
Pubbl/distr/stampa Cambridge, UK, : Royal Society of Chemistry, 2002
Descrizione fisica 1 online resource (181 p.)
Disciplina 547.412
Altri autori (Persone) TaylorPeter
GaganMichael
Collana The molecular world
Soggetto topico Alkenes
Aromatic compounds
Soggetto genere / forma Electronic books.
ISBN 1-84755-782-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto BK9780854046805-FX001; BK9780854046805-FP001; BK9780854046805-FP003; BK9780854046805-FP005; BK9780854046805-FP009; BK9780854046805-00011; BK9780854046805-00028; BK9780854046805-00032; BK9780854046805-00033; BK9780854046805-00036; BK9780854046805-00037; BK9780854046805-00039; BK9780854046805-00042; BK9780854046805-00045; BK9780854046805-00061; BK9780854046805-00068; BK9780854046805-00075; BK9780854046805-00077; BK9780854046805-00078; BK9780854046805-00088; BK9780854046805-00089; BK9780854046805-00091; BK9780854046805-00096; BK9780854046805-00101; BK9780854046805-00102; BK9780854046805-00111
BK9780854046805-00122BK9780854046805-00124; BK9780854046805-00130; BK9780854046805-00131; BK9780854046805-00136; BK9780854046805-00137; BK9780854046805-00139; BK9780854046805-00144; BK9780854046805-00162; BK9780854046805-00170; BK9780854046805-00172; BK9780854046805-00173; BK9780854046805-00184
Record Nr. UNINA-9910455115503321
Cambridge, UK, : Royal Society of Chemistry, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Alkenes and aromatics [[electronic resource] /] / edited by Peter Taylor [and Michael Gagan]
Alkenes and aromatics [[electronic resource] /] / edited by Peter Taylor [and Michael Gagan]
Pubbl/distr/stampa Cambridge, UK, : Royal Society of Chemistry, 2002
Descrizione fisica 1 online resource (181 p.)
Disciplina 547.412
Altri autori (Persone) TaylorPeter
GaganMichael
Collana The molecular world
Soggetto topico Alkenes
Aromatic compounds
ISBN 1-84755-782-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto BK9780854046805-FX001; BK9780854046805-FP001; BK9780854046805-FP003; BK9780854046805-FP005; BK9780854046805-FP009; BK9780854046805-00011; BK9780854046805-00028; BK9780854046805-00032; BK9780854046805-00033; BK9780854046805-00036; BK9780854046805-00037; BK9780854046805-00039; BK9780854046805-00042; BK9780854046805-00045; BK9780854046805-00061; BK9780854046805-00068; BK9780854046805-00075; BK9780854046805-00077; BK9780854046805-00078; BK9780854046805-00088; BK9780854046805-00089; BK9780854046805-00091; BK9780854046805-00096; BK9780854046805-00101; BK9780854046805-00102; BK9780854046805-00111
BK9780854046805-00122BK9780854046805-00124; BK9780854046805-00130; BK9780854046805-00131; BK9780854046805-00136; BK9780854046805-00137; BK9780854046805-00139; BK9780854046805-00144; BK9780854046805-00162; BK9780854046805-00170; BK9780854046805-00172; BK9780854046805-00173; BK9780854046805-00184
Record Nr. UNINA-9910778211303321
Cambridge, UK, : Royal Society of Chemistry, 2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
Autore Ulrich Henri <1925->
Pubbl/distr/stampa Hoboken, NJ, : Wiley, 2009
Descrizione fisica 1 online resource (566 p.)
Disciplina 547.2
547.412
Soggetto topico Alkenes
Chemical reactions
Soggetto genere / forma Electronic books.
ISBN 1-282-46107-9
9786612461071
0-470-74795-1
0-470-74793-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 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
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
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 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
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
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
7.3.3 Sulfur Trioxide, O SO2
Record Nr. UNINA-9910139957803321
Ulrich Henri <1925->  
Hoboken, NJ, : Wiley, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
Cumulenes in click reactions [[electronic resource] /] / Henri Ulrich
Autore Ulrich Henri <1925->
Pubbl/distr/stampa Hoboken, NJ, : Wiley, 2009
Descrizione fisica 1 online resource (566 p.)
Disciplina 547.2
547.412
Soggetto topico Alkenes
Chemical reactions
ISBN 1-282-46107-9
9786612461071
0-470-74795-1
0-470-74793-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 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
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
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 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
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
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
7.3.3 Sulfur Trioxide, O SO2
Record Nr. UNINA-9910831093303321
Ulrich Henri <1925->  
Hoboken, NJ, : Wiley, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cumulenes in click reactions / / Henri Ulrich
Cumulenes in click reactions / / Henri Ulrich
Autore Ulrich Henri <1925->
Pubbl/distr/stampa Hoboken, NJ, : Wiley, 2009
Descrizione fisica 1 online resource (566 p.)
Disciplina 547.2
547.412
Soggetto topico Alkenes
Chemical reactions
ISBN 1-282-46107-9
9786612461071
0-470-74795-1
0-470-74793-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 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
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
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 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
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
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
7.3.3 Sulfur Trioxide, O SO2
Record Nr. UNINA-9910877710203321
Ulrich Henri <1925->  
Hoboken, NJ, : Wiley, 2009
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Handbook of metathesis . Volume 2 Applications in organic synthesis / / editors, Prof. Robert H. Grubbs, Prof. Daniel J. O'Leary
Handbook of metathesis . Volume 2 Applications in organic synthesis / / editors, Prof. Robert H. Grubbs, Prof. Daniel J. O'Leary
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2015
Descrizione fisica 1 online resource (772 p.)
Disciplina 660.299
Soggetto topico Metathesis (Chemistry)
Alkenes
Organic compounds - Synthesis
ISBN 3-527-69404-8
3-527-69402-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Contents; Preface; List of Contributors; List of Abbreviations; Chapter 1 General Ring-Closing Metathesis; 1.1 Introduction; 1.2 Carbocycles (Introduction); 1.2.1 Small-Sized Carbocycles; 1.2.2 Medium-Sized Carbocycles; 1.2.3 Spiro Carbocycles; 1.3 Synthesis of Bridged Bicycloalkenes; 1.4 Synthesis of Heterocycles Containing Si, P, S, or B; 1.4.1 Si-Heterocycles; 1.4.2 P-Heterocycles; 1.4.3 S-Heterocycles; 1.4.4 B-Heterocycles; 1.5 Synthesis of O-Heterocycles; 1.5.1 Small and Medium-Size Cyclic Ethers; 1.5.2 Polycyclic Ethers; 1.6 Synthesis of N-Heterocycles; 1.6.1 N-Heterocycles
1.6.2 Small and Medium-Sized Lactams1.7 Synthesis of Cyclic Conjugated Dienes; 1.8 Alkyne Metathesis; 1.9 Enyne Metathesis; 1.9.1 General Enyne Metathesis; 1.9.2 Dienyne Metathesis; 1.10 Tandem Processes; 1.10.1 Tandem ROM/RCM; 1.10.2 Other Tandem RCMs; 1.11 Synthesis of Macrocycles; 1.11.1 Macrocycles; 1.11.2 Macrolactones; 1.11.3 Macrolactams; 1.12 RCM and Isomerization via Ru-H; 1.13 Relay RCM (RRCM); 1.14 Z-Selective RCM; 1.14.1 Substrate-Controlled Z-Selective RCM; 1.14.2 Catalyst-Controlled Z-Selective RCM; 1.15 Enantioselective RCM; 1.16 Conclusion; Acknowledgments; References
Chapter 2 Cross-Metathesis2.1 Early Examples Using Well-Defined Molybdenum and Ruthenium Catalysts; 2.2 The General Model for Selectivity in CM Reactions; 2.3 Definition of Cross-Metathesis Reaction Categories and Chapter Organization; 2.4 Hydrocarbons; 2.4.1 Alkane Extensions; 2.4.2 Unsaturated Hydrocarbons, Including Styrene; 2.4.3 Ethylene Cross-Metathesis; 2.5 Boron; 2.6 Nitrogen; 2.6.1 Amines; 2.6.2 Amines as CM Partners in Heterocycle Syntheses; 2.6.3 Acrylonitrile and Other Nitrile-Based CM Applications; 2.6.4 Other Nitrogenous Substrates; 2.7 Oxygen
2.7.1 Primary Allylic Alcohols and Derivatives2.7.2 Secondary Allylic Alcohols and Derivatives; 2.7.3 Tertiary Allylic Alcohols and Derivatives; 2.7.4 Homoallylic Alcohols and Derivatives; 2.7.5 Vinyl Ethers; 2.7.6 Acrolein, Crotonaldehyde, and Methacrolein; 2.7.7 Methyl Vinyl Ketone and Related Systems; 2.7.8 Acrylic Acid; 2.7.9 Acrylic Acid Derivatives, Including Esters, Thioesters, and Amides; 2.8 Halides; 2.9 Phosphorus; 2.10 Sulfur; 2.11 Fragment Coupling Reactions; 2.11.1 Acetogenins; 2.11.2 Cross-Metathesis Selectivity; 2.11.3 Tuning Metathesis Selectivity
2.11.4 CM as an Alternative Coupling Strategy2.11.5 CM-Based Analog Synthesis; 2.11.6 Polyene Metathesis; 2.11.7 Cross-Metathesis Reaction Optimization: Pinnaic Acid; 2.12 Conclusions; References; Chapter 3 Vignette: Extending the Application of Metathesis in Chemical Biology - The Development of Site-Selective Peptide and Protein Modifications; 3.1 Introduction; 3.2 Cross-Metathesis Methodology Studies in Aqueous Media; 3.2.1 Allyl Sulfides are Reactive Substrates in Olefin Metathesis; 3.2.2 Sulfur-Relayed Cross-Metathesis
3.2.3 Application of Aqueous Metathesis of Allyl Sulfides in Synthesis
Record Nr. UNINA-9910787418903321
Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2015
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Handbook of metathesis . Volume 2 Applications in organic synthesis / / editors, Prof. Robert H. Grubbs, Prof. Daniel J. O'Leary
Handbook of metathesis . Volume 2 Applications in organic synthesis / / editors, Prof. Robert H. Grubbs, Prof. Daniel J. O'Leary
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2015
Descrizione fisica 1 online resource (772 p.)
Disciplina 660.299
Soggetto topico Metathesis (Chemistry)
Alkenes
Organic compounds - Synthesis
ISBN 3-527-69404-8
3-527-69402-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Contents; Preface; List of Contributors; List of Abbreviations; Chapter 1 General Ring-Closing Metathesis; 1.1 Introduction; 1.2 Carbocycles (Introduction); 1.2.1 Small-Sized Carbocycles; 1.2.2 Medium-Sized Carbocycles; 1.2.3 Spiro Carbocycles; 1.3 Synthesis of Bridged Bicycloalkenes; 1.4 Synthesis of Heterocycles Containing Si, P, S, or B; 1.4.1 Si-Heterocycles; 1.4.2 P-Heterocycles; 1.4.3 S-Heterocycles; 1.4.4 B-Heterocycles; 1.5 Synthesis of O-Heterocycles; 1.5.1 Small and Medium-Size Cyclic Ethers; 1.5.2 Polycyclic Ethers; 1.6 Synthesis of N-Heterocycles; 1.6.1 N-Heterocycles
1.6.2 Small and Medium-Sized Lactams1.7 Synthesis of Cyclic Conjugated Dienes; 1.8 Alkyne Metathesis; 1.9 Enyne Metathesis; 1.9.1 General Enyne Metathesis; 1.9.2 Dienyne Metathesis; 1.10 Tandem Processes; 1.10.1 Tandem ROM/RCM; 1.10.2 Other Tandem RCMs; 1.11 Synthesis of Macrocycles; 1.11.1 Macrocycles; 1.11.2 Macrolactones; 1.11.3 Macrolactams; 1.12 RCM and Isomerization via Ru-H; 1.13 Relay RCM (RRCM); 1.14 Z-Selective RCM; 1.14.1 Substrate-Controlled Z-Selective RCM; 1.14.2 Catalyst-Controlled Z-Selective RCM; 1.15 Enantioselective RCM; 1.16 Conclusion; Acknowledgments; References
Chapter 2 Cross-Metathesis2.1 Early Examples Using Well-Defined Molybdenum and Ruthenium Catalysts; 2.2 The General Model for Selectivity in CM Reactions; 2.3 Definition of Cross-Metathesis Reaction Categories and Chapter Organization; 2.4 Hydrocarbons; 2.4.1 Alkane Extensions; 2.4.2 Unsaturated Hydrocarbons, Including Styrene; 2.4.3 Ethylene Cross-Metathesis; 2.5 Boron; 2.6 Nitrogen; 2.6.1 Amines; 2.6.2 Amines as CM Partners in Heterocycle Syntheses; 2.6.3 Acrylonitrile and Other Nitrile-Based CM Applications; 2.6.4 Other Nitrogenous Substrates; 2.7 Oxygen
2.7.1 Primary Allylic Alcohols and Derivatives2.7.2 Secondary Allylic Alcohols and Derivatives; 2.7.3 Tertiary Allylic Alcohols and Derivatives; 2.7.4 Homoallylic Alcohols and Derivatives; 2.7.5 Vinyl Ethers; 2.7.6 Acrolein, Crotonaldehyde, and Methacrolein; 2.7.7 Methyl Vinyl Ketone and Related Systems; 2.7.8 Acrylic Acid; 2.7.9 Acrylic Acid Derivatives, Including Esters, Thioesters, and Amides; 2.8 Halides; 2.9 Phosphorus; 2.10 Sulfur; 2.11 Fragment Coupling Reactions; 2.11.1 Acetogenins; 2.11.2 Cross-Metathesis Selectivity; 2.11.3 Tuning Metathesis Selectivity
2.11.4 CM as an Alternative Coupling Strategy2.11.5 CM-Based Analog Synthesis; 2.11.6 Polyene Metathesis; 2.11.7 Cross-Metathesis Reaction Optimization: Pinnaic Acid; 2.12 Conclusions; References; Chapter 3 Vignette: Extending the Application of Metathesis in Chemical Biology - The Development of Site-Selective Peptide and Protein Modifications; 3.1 Introduction; 3.2 Cross-Metathesis Methodology Studies in Aqueous Media; 3.2.1 Allyl Sulfides are Reactive Substrates in Olefin Metathesis; 3.2.2 Sulfur-Relayed Cross-Metathesis
3.2.3 Application of Aqueous Metathesis of Allyl Sulfides in Synthesis
Record Nr. UNINA-9910828172403321
Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2015
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