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Isolated pyranones multifaceted building blocks for molecular diversity /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Ram, Vishnu Ji
Otros Autores: Goel, Atul, Pratap, Ramendra
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Elsevier, 2022.
Temas:
Acceso en línea:Texto completo

MARC

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040 |a YDX  |b eng  |c YDX  |d OPELS  |d EBLCP  |d OCLCO  |d OCLCF  |d N$T  |d OCLCQ 
020 |a 9780128232125  |q (electronic bk.) 
020 |a 0128232129  |q (electronic bk.) 
020 |z 9780128212165 
020 |z 0128212160 
035 |a (OCoLC)1313387208 
050 4 |a QD405 
082 0 4 |a 547.592  |2 23 
100 1 |a Ram, Vishnu Ji. 
245 1 0 |a Isolated pyranones  |h [electronic resource] :  |b multifaceted building blocks for molecular diversity /  |c Vishnu Ji Ram, Atul Goel and Ramendra Pratap. 
260 |a Amsterdam :  |b Elsevier,  |c 2022. 
300 |a 1 online resource 
500 |a Includes index. 
505 0 |a Front Cover -- Isolated Pyranones -- Copyright Page -- Contents -- Preface -- 1 Introduction -- References -- 2 Characteristics of pyranones -- References -- 3 Chemistry of isolated 2-pyranones -- Subchapter 3.1 2H-Pyran-2-one -- 3.1.1 Introduction -- 3.1.2 Characteristics of 2-pyranones -- 3.1.3 Synthesis of 2H-pyran-2-ones -- 3.1.3.1 Condensation-cyclization approach -- 3.1.3.2 By Wittig reaction -- 3.1.3.3 By intramolecular cyclization approach -- 3.1.3.4 From silyl reagents -- 3.1.3.5 From (Z)-2-en-4-ynoic acids -- 3.1.3.6 From cyclization of glutaconic acid 
505 8 |a 3.1.4 Reactivity of 2H-pyran-2-ones -- 3.1.5 Electrophilic addition and substitution reaction -- 3.1.5.1 Halogenation -- 3.1.5.2 Chloromethylation -- 3.1.5.3 Nitration -- 3.1.5.4 Alkylation reactions -- 3.1.5.5 Nucleophilic reactions -- 3.1.5.5.1 Reactions of C-nucleophiles -- 3.1.5.6 Reaction of pyran with Grignard reagent -- 3.1.5.7 Reaction with diazomethane -- 3.1.5.8 Reaction with cyanide anion -- 3.1.6 C-Nucleophile-induced ring transformations -- 3.1.6.1 Reaction with dialkyl ketones -- 3.1.6.2 Reaction with hexane-5-one -- 3.1.6.3 Reaction with aryl methyl ketone 
505 8 |a 3.1.6.4 Reaction with malononitrile -- 3.1.6.5 Reaction with phenylacetonitrile and 2-cyanomethylbenzonitrile -- 3.1.6.6 Reaction with 2-methyl-5-nitrobenzonitrile -- 3.1.6.7 Reaction with allyl cyanide -- 3.1.6.8 Reaction with 2-(1-arylethylidene)malononitriles -- 3.1.6.9 Reaction with arylacetones -- 3.1.6.10 Reaction with ethyl levulinate -- 3.1.6.11 Reaction with methyl vinyl ketone -- 3.1.6.12 Reaction with 2-methoxyacetophenone -- 3.1.6.13 Reaction with isopropyl methyl ketone -- 3.1.6.14 Reaction with 2-cyanomethylpyridne 
505 8 |a 3.1.6.15 Reaction with (5-aryl-1H-pyrazol-3-yl)-/(benzimidazol-2-yl)-/(benzothiazol-2-yl)-acetonitriles -- 3.1.7 Synthesis of 1,2-diaryl-, 1,2,3-triaryl-, 1,2,4-triaryl-, and 1,2,3,4-tetraarylbenzenes -- 3.1.8 Synthesis of fused compounds -- 3.1.9 Synthesis of functionalized benzaldehyde and 2-tetralones -- 3.1.10 Synthesis of metallocenes -- 3.1.11 Nitrogen nucleophile-induced reactions -- 3.1.12 Reaction with ammonia source, hydrazine, hydroxylamines, and different amines -- 3.1.13 Reaction with guanidines -- 3.1.14 Reaction with amidines -- 3.1.15 Reaction with benzamides 
505 8 |a 3.1.16 Reaction with oxoketene cyclic aminals -- 3.1.17 S-nucleophile-induced ring transformation reactions -- 3.1.18 Miscellaneous reactions -- 3.1.18.1 Carbanion-induced ring contraction reactions -- 3.1.18.2 Ring-opening reactions -- 3.1.18.3 Reactions at substituents -- 3.1.19 Reduction -- 3.1.20 Photochemical reactions -- 3.1.21 Cycloaddition reactions -- 3.1.22 Miscellaneous reaction -- 3.1.23 Conclusion -- Subchapter 3.2 Dihydro 2H-pyran-2-ones -- 3.2.1 3,4-Dihydro-2H-pyran-2-one -- 3.2.2 Chemical reactivity -- 3.2.2.1 5,6-Dihydro-2H-pyran-2-one (5,6-dihydropyran-2-one) 
650 0 |a Pyran. 
650 7 |a Pyran.  |2 fast  |0 (OCoLC)fst01084595 
700 1 |a Goel, Atul. 
700 1 |a Pratap, Ramendra. 
776 0 8 |i Print version:  |z 9780128232125 
776 0 8 |i Print version:  |z 0128212160  |z 9780128212165  |w (OCoLC)1244618078 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128212165  |z Texto completo