Perhalopyridines

Halogenated pyridines can be used as interesting starting materials in a wide range of organic synthesis methods. Substituted pyridine compounds are used generally as starting materials in the nucleophilic substitution reactions and have unique scaffolds for the construction of other heterocyclic an...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Ranjbar-Karimi, Reza
Otros Autores: Poorfreidoni, Alireza
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Singapore : Bentham Science Publishers, 2020.
Temas:
Chemistry.
Chimie.
chemistry.
Chemistry
Acceso en línea:Texto completo

MARC

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049 |a UAMI 
100 1 |a Ranjbar-Karimi, Reza. 
245 1 0 |a Perhalopyridines  |h [electronic resource]. 
260 |a Singapore :  |b Bentham Science Publishers,  |c 2020. 
300 |a 1 online resource (256 p.) 
500 |a Description based upon print version of record. 
505 0 |a Cover -- Title -- Copyright -- End User License Agreement -- Contents -- Preface -- CONSENT FOR PUBLICATION -- CONFLICT OF INTEREST -- ACKNOWLEDGEMENTS -- Foreword -- Abbreviations -- Properties of Perhalopyridines -- 1. PHYSICAL AND CHEMICAL PROPERTIES -- 2. SPECTROSCOPY -- 3. REACTIONS -- REFERENCES -- Perfluoropyridines -- 1. INTRODUCTION -- 2. SYNTHESIS OF PENTAFLUOROPYRIDINE -- 3. REACTION MECHANISM -- 4. REACTION OF PENTAFLUOROPYRIDINE WITH VARIOUS MONO DENTATE NUCLEOPHILES -- 4.1. Reaction of S-centered Nucleophile with Pentafluoropyridine 
505 8 |a 4.2. Reaction of O-centered Nucleophile with Pentafluoropyridine -- 4.3. Reaction of C-centered Nucleophile with Pentafluoropyridine -- 4.4. Reaction of N-centered Nucleophile with Pentafluoropyridine -- 4.5. Reaction of Pentafluoropyridine 3 with Halogenating Reagents (Cl, Br, I) -- 4.6. Reduction of Perfluorinated Pyridines -- 5. REACTION OF PERFLUOROPYRIDINES WITH VARIOUS MULTIDENTATE NUCLEOPHILES -- 5.1. Synthesis of Perfluorinated Heterocyles -- 5.2. Synthesis of Fluorinated Ring-fused Heterocyles -- 6. ORGANOMETALLIC COMPOUNDS OF PERFLUORO- HETEROAROMATICS 
505 8 |a 7. PHOTOCHEMICAL REACTIONS OF FLUORINATED PYRIDINES -- 8. COPOLYMERIZATION OF PENTAFLUOROPYRIDINE -- 9. THE PENTAFLUOROPYRIDINE CATION C5F5N+ -- 10. SALTS OF PERFLUOROPYRIDINE -- 11. SYNTHESIS OF MACROCYCLIC COMPOUNDS FROM POLYFLUOROPYRIDINES -- 12. PENTAFLUOROPYRIDINE IN MEDICINAL CHEMISTRY AND BIOCHEMISTRY -- REFERENCES -- Perchloropyridines -- 1. INTRODUCTION -- 2. SYNTHESIS OF PENTACHLOROPYRIDINE -- 2.1. By Straight Chlorination -- 2.2. By Ring-closing Method -- 2.3. Synthesis of Pentachloropyridine-1-15N-2,6-13C2 -- 3. NUCLEOPHILIC REACTIONS OF PERCHLOROPYRIDINES 
505 8 |a 3.1. Reaction of Pentachloropyridine with Various Mono Dentate Nucleophiles -- 3.1.1. Reaction of N-centered Nucleophile with Pentachloropyridine -- 3.1.2. Reaction of S-centered Nucleophile with Pentachloropyridine -- 3.1.3. Reaction of C-centered Nucleophile with Perchloropyridines -- 3.2. Reaction of Perchloropyridines with Bidentate Nucleophiles -- 4. CROSS-COUPLING REACTIONS OF PERCHLOROPYRIDINES -- 5. BROMINATION OF PENTACHLOROPYRIDINE -- 6. OXIDATION OF POLYCHLOROPYRIDINES -- 7. REDUCTION OF POLYCHLOROPYRIDINES -- 8. ALKYLATION OF POLYCHLOROPYRIDINES 
505 8 |a 9. PHOTOCHEMICAL REACTIONS OF POLYCHLOROPYRIDINES -- 10. ORGANOMETALLIC REAGENTS OF PERCHLOROPYRIDINE -- REFERENCES -- Perbromopyridines -- 1. SYNTHESIS OF PENTABROMOPYRIDINE -- 2. NUCLEOPHILIC REACTIONS OF PENTABROMOPYRIDINE -- 2.1. Reaction of O-centered Nucleophile with Pentabromopyridine -- 2.2. Reaction of N-centered Nucleophile with Pentabromopyridine -- 2.3. Reaction of S-centered Nucleophile with Pentabromopyridine -- 3. ORGANOMETALIC REAGENT OF POLYBROMOPYRIDINES -- 4. SALTS OF PENTABROMOPYRIDINE -- 5. OXIDATION OF PENTABROMOPYRIDINE -- 6. PHOTOCHEMICAL REACTIONS OF PENTABROMOPYRIDINE 
500 |a 7. SYNTHESIS AND REACTIONS OF 2,4,6-TRIBROMO-3,5-DIFLUOROPYRIDINE. 
520 |a Halogenated pyridines can be used as interesting starting materials in a wide range of organic synthesis methods. Substituted pyridine compounds are used generally as starting materials in the nucleophilic substitution reactions and have unique scaffolds for the construction of other heterocyclic and macrocyclic compounds. They also have important medicinal properties. Due to synthetic difficulties in the synthesis of the highly substituted pyridine derivatives from pyridine itself, perhalopyridines have a special importance in this regard. This book covers the synthetic reactions and applicat. 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
650 0 |a Chemistry. 
650 6 |a Chimie. 
650 7 |a chemistry.  |2 aat 
650 7 |a Chemistry  |2 fast 
700 1 |a Poorfreidoni, Alireza. 
758 |i has work:  |a Perhalopyridines (Text)  |1 https://id.oclc.org/worldcat/entity/E39PD3B6D9G6qf3bBvC83P8CjP  |4 https://id.oclc.org/worldcat/ontology/hasWork 
776 0 8 |i Print version:  |a Ranjbar-Karimi, Reza  |t Perhalopyridines: Synthesis and Synthetic Utility  |d Singapore : Bentham Science Publishers,c2020  |z 9789811473777 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=6371153  |z Texto completo 
938 |a ProQuest Ebook Central  |b EBLB  |n EBL6371153 
938 |a YBP Library Services  |b YANK  |n 301540904 
994 |a 92  |b IZTAP 

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