Nitro Compounds and Their Derivatives in Organic Synthesis

Nitro chemistry plays an important role in organic synthesis to construct new frameworks. This is due to the diverse properties of the nitro group. The strong electron-withdrawing ability of the nitro group reduces the electron density of the scaffold, facilitating reactions with nucleophiles or ele...

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Other Authors: Nishiwaki, Nagatoshi (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2020
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DOAB: description of the publication
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520 |a Nitro chemistry plays an important role in organic synthesis to construct new frameworks. This is due to the diverse properties of the nitro group. The strong electron-withdrawing ability of the nitro group reduces the electron density of the scaffold, facilitating reactions with nucleophiles or electron transfer. In addition, the -hydrogen of the nitro group is highly acidic, giving a stable anion, which facilitates reactions with both electrophilic and nucleophilic reagents. In addition, the nitro group also serves as a good leaving group, which facilitates transformation to a wide variety of functional groups. Despite the substantial contributions of many researchers, nitro chemistry is still an exciting and challenging research area. This book brings together recent original research and review articles contributed by an international team of leading experts and pioneers in organic synthesis using nitro groups. It is sure to provide useful information and promising insights for researchers. 
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653 |a nitro 
653 |a pyridone 
653 |a 1-methyl-2-quinolone 
653 |a cycloaddition 
653 |a direct functionalization 
653 |a perylenediimide 
653 |a nitro group 
653 |a organic materials 
653 |a Phenacylation of beta-nitropyridin-2-ones 
653 |a 8-nitro-5-RO-indolizines 
653 |a oxazole-pyrrole ring transformation 
653 |a conjugate addition 
653 |a dihydrofuran 
653 |a 1,3-dicarbonyl compound 
653 |a enolate 
653 |a isoxazoline N-oxide 
653 |a nitroketone 
653 |a nitronate 
653 |a nucleophilic substitution 
653 |a nitropyridines 
653 |a isoxazolo[4,3-b]pyridines 
653 |a 1,4-dihydropyridines 
653 |a nucleophilic addition 
653 |a Diels-Alder reaction 
653 |a dearomatization 
653 |a hexapyrrolohexaazacoronene 
653 |a nitration 
653 |a SNAr substitution 
653 |a ICT character 
653 |a aromaticity 
653 |a C-H functionalization 
653 |a total synthesis 
653 |a pyrrolidines 
653 |a anchimeric assistance 
653 |a epimerization 
653 |a PDE4 inhibitors 
653 |a 1,3-Dipole 
653 |a electron-withdrawing ability 
653 |a electrophilicity 
653 |a nucleophilicity 
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