Strategies for palladium-catalyzed non-directed and directed C-H bond functionalization /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Kapdi, Anant R., Maiti, Debabrata
Formato: Electrónico eBook
Idioma:Inglés
Publicado: [Place of publication not identified] : Elsevier, 2017.
Colección:Latest trends in palladium chemistry.
Temas:
Organometallic chemistry.
Chemical bonds.
Catalysis.
Activation (Chemistry)
Carbon.
Hydrogen.
Catalysis
Carbon
Hydrogen
Chimie organom�etallique.
Catalyse.
Activation (Chimie)
Carbone.
Hydrog�ene.
SCIENCE / Chemistry / Organic.
Acceso en línea:Texto completo

MARC

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245 0 0 |a Strategies for palladium-catalyzed non-directed and directed C-H bond functionalization /  |c edited by Anant R. Kapdi, Debabrata Maiti. 
260 |a [Place of publication not identified] :  |b Elsevier,  |c 2017. 
300 |a 1 online resource (xiv, 486 pages) :  |b illustrations. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Latest trends in Palladium Chemistry 
505 0 0 |g Machine generated contents note:  |g 1.  |t Introduction /  |r Debabrata Maiti --  |g 2.  |t Directed C -- H Bond Functionalization Strategies for Synthesis /  |r Anant R. Kapdi --  |g 2.1.  |t Introduction --  |g 2.2.  |t Ortho-Palladated C -- H Bond Functionalization via Directing Group Effect --  |g 2.3.  |t Conclusion --  |t References --  |g 3.  |t Nondirected C -- H Bond Functionalizations of (Hetero)arenes /  |r Fuk-Yee Kwong --  |g 3.1.  |t Introduction --  |g 3.2.  |t Reactions With Halides --  |g 3.3.  |t Reactions With Pseudohalides --  |g 3.4.  |t Conclusion --  |t References --  |g 4.  |t Palladium-Catalyzed Directed Arylation of Unactivated C(sp3) -- H Bonds /  |r Bing-Feng Shi --  |g 4.1.  |t Introduction --  |g 4.2.  |t Palladium-Catalyzed C(sp3) -- H Arylation Directed by Monodentate DGs --  |g 4.3.  |t Palladium-Catalyzed C(sp3) -- H Arylation Directed by Bidentate DGs --  |g 4.4.  |t Palladium-Catalyzed C(sp3) -- H Arylation Using Transient DGs --  |g 4.5.  |t Palladium-Catalyzed Asymmetric C(sp3) -- H Arylation --  |g 4.6.  |t Conclusions and Outlook --  |t References --  |g 5.  |t C -- H Bond Functionalization at the Benzene Core of Indoles and Indolines (Excluding C-2 and C-3) /  |r Martin Oestreich --  |g 5.1.  |t Palladium-Catalyzed C -- H Bond Functionalization of Indole --  |g 5.2.  |t Palladium-Catalyzed C -- H Bond Functionalization of Indolines --  |g 5.3.  |t Conclusions --  |t List of Abbreviations --  |t References --  |g 6.  |t Palladium-Catalyzed Carbonylative and Carboxylative C -- H Functionalization Reactions: Importance and Role of Regioselectivity /  |r Bhalchandra M. Bhanage --  |g 6.1.  |t Introduction --  |g 6.2.  |t Carbonylative C -- H Functionalization of Arenes in the Presence of Directing Group --  |g 6.3.  |t Carbonylative C(sp2) -- H Functionalization of Heteroarenes --  |g 6.4.  |t Carboxylative C -- H Bond Functionalization --  |g 6.5.  |t Conclusion and Future Outlook --  |t References --  |g 7.  |t Flow Chemistry Perspective for C -- H Bond Functionalization /  |r Timothy Noel --  |g 7.1.  |t Introduction --  |g 7.2.  |t Advantages of Using Continuous-Flow Microreactor Technology for C -- H Activation --  |g 7.3.  |t Cross-Dehydrogenative Coupling in Continuous Flow --  |g 7.4.  |t Rh-Catalyzed C -- H Activation Reactions in Continuous Flow --  |g 7.5.  |t Palladium-Catalyzed C(sp3) -- H Activation Reactions in Continuous Flow --  |g 7.6.  |t Ru-Catalyzed C -- H Activation Reactions in Continuous Flow --  |g 7.7.  |t Intramolecular C -- H Activation Reactions in Continuous Flow --  |g 7.8.  |t Ortho-Directed Hydrogen/Deuterium Isotope Exchange via Iridium-Catalyzed C -- H Activation --  |g 7.9.  |t Conclusion --  |t References --  |g 8.  |t Directed Meta-Selective C -- H Bond Functionalizations /  |r Gang Li --  |g 8.1.  |t Introduction --  |g 8.2.  |t Directing Group Assisted Meta-C -- H Functionalization --  |g 8.3.  |t Ortho-Directing Group-Assisted and Norbornene-Mediated Meta-C -- H Functionalization --  |g 8.4.  |t Formal Meta-C -- H Functionalization Using a Traceless Directing Group --  |g 8.5.  |t Conclusion --  |t Abbreviations --  |t References --  |g 9.  |t Recent Advances in Distal Aliphatic sp3 C -- H Functionalization /  |r Debabrata Maiti --  |g 9.1.  |t Introduction --  |g 9.2.  |t Scope of Functionalization --  |g 9.4.  |t Conclusion --  |t References --  |g 10.  |t Palladacycles for Directed and Nondirected C -- H Bond Functionalization of (Hetero)arenes /  |r Benudhar Punji --  |g 10.1.  |t Introduction --  |g 10.2.  |t Palladacycle PreCatalyst in C -- H Functionalization --  |g 10.3.  |t Palladacycle Intermediate in C -- H Functionalization --  |g 10.4.  |t Conclusion --  |t Abbreviations --  |t References --  |g 11.  |t Mechanistic/Organometallic Aspects of Palladium-Catalyzed C -- H Bond Functionalization /  |r Anant R. Kapdi --  |g 11.1.  |t Introduction --  |g 11.2.  |t Early Findings --  |g 11.3.  |t Palladium-Catalyzed C -- H Activation Pathways --  |g 11.4.  |t Conclusion --  |t Acknowledgments --  |t List of Abbreviations --  |t References --  |g 12.  |t Recent Developments in Palladium-Catalyzed Natural Product Synthesis via C -- H Activation /  |r Chandra M.R. Volla --  |g 12.1.  |t Introduction --  |g 12.2.  |t Total Synthesis of Aspidospermidine --  |g 12.3.  |t Total Synthesis of (+) -Lithospermic Acid --  |g 12.4.  |t Total Synthesis of Pipercyclobutanamide A --  |g 12.5.  |t Total Synthesis of Piperarborenine B and D --  |g 12.6.  |t Total Synthesis of Podophyllatoxin --  |g 12.7.  |t Total Synthesis of Clavicipitic Acid --  |g 12.8.  |t Total Synthesis of Hibispeptin A --  |g 12.9.  |t Divergent Synthesis of Aeruginosins (sp3 C -- H Alkenylation and Arylation) --  |g 12.10.  |t Total Synthesis of (+) Linoxepin --  |g 12.11.  |t Rapid Total Synthesis of Rhazinal --  |g 12.12.  |t Total Synthesis of Gamendazole --  |g 12.13.  |t Total Synthesis of (+/- ) Rhazinilam --  |g 12.14.  |t Conclusion --  |t References. 
504 |a Includes bibliographical references and index. 
650 0 |a Organometallic chemistry. 
650 0 |a Chemical bonds. 
650 0 |a Catalysis. 
650 0 |a Activation (Chemistry) 
650 0 |a Carbon. 
650 0 |a Hydrogen. 
650 2 |a Catalysis  |0 (DNLM)D002384 
650 2 |a Carbon  |0 (DNLM)D002244 
650 2 |a Hydrogen  |0 (DNLM)D006859 
650 6 |a Chimie organom�etallique.  |0 (CaQQLa)201-0154573 
650 6 |a Catalyse.  |0 (CaQQLa)201-0025978 
650 6 |a Activation (Chimie)  |0 (CaQQLa)201-0279727 
650 6 |a Carbone.  |0 (CaQQLa)201-0007763 
650 6 |a Hydrog�ene.  |0 (CaQQLa)201-0023816 
650 7 |a SCIENCE / Chemistry / Organic.  |2 bisacsh 
650 7 |a Activation (Chemistry)  |2 fast  |0 (OCoLC)fst00796267 
650 7 |a Carbon.  |2 fast  |0 (OCoLC)fst00846775 
650 7 |a Catalysis.  |2 fast  |0 (OCoLC)fst00848867 
650 7 |a Chemical bonds.  |2 fast  |0 (OCoLC)fst00852856 
650 7 |a Hydrogen.  |2 fast  |0 (OCoLC)fst00964990 
650 7 |a Organometallic chemistry.  |2 fast  |0 (OCoLC)fst01047969 
700 1 |a Kapdi, Anant R. 
700 1 |a Maiti, Debabrata. 
776 0 8 |i Print version.  |t Strategies for palladium-catalyzed non-directed and directed C-H bond functionalization.  |d Amsterdam, Netherlands ; Cambridge, MA : Elsevier, �2017  |z 9780128052549  |w (DLC) 2017302021  |w (OCoLC)959885627 
830 0 |a Latest trends in palladium chemistry. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128052549  |z Texto completo 

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