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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| Year of Publication: | 2020 |
| Language: | English |
| Physical Description: | 1 electronic resource (120 p.) |
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Nishiwaki, Nagatoshi edt Nitro Compounds and Their Derivatives in Organic Synthesis Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2020 1 electronic resource (120 p.) text txt rdacontent computer c rdamedia online resource cr rdacarrier 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. English Research & information: general bicssc nitro pyridone 1-methyl-2-quinolone cycloaddition direct functionalization perylenediimide nitro group organic materials Phenacylation of beta-nitropyridin-2-ones 8-nitro-5-RO-indolizines oxazole-pyrrole ring transformation conjugate addition dihydrofuran 1,3-dicarbonyl compound enolate isoxazoline N-oxide nitroketone nitronate nucleophilic substitution nitropyridines isoxazolo[4,3-b]pyridines 1,4-dihydropyridines nucleophilic addition Diels-Alder reaction dearomatization hexapyrrolohexaazacoronene nitration SNAr substitution ICT character aromaticity C–H functionalization total synthesis pyrrolidines anchimeric assistance epimerization PDE4 inhibitors 1,3-Dipole electron-withdrawing ability electrophilicity nucleophilicity 3-03943-148-X 3-03943-149-8 Nishiwaki, Nagatoshi oth |
| language |
English |
| format |
eBook |
| author2 |
Nishiwaki, Nagatoshi |
| author_facet |
Nishiwaki, Nagatoshi |
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n n nn |
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Sonstige |
| title |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| spellingShingle |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_full |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_fullStr |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_full_unstemmed |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_auth |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_new |
Nitro Compounds and Their Derivatives in Organic Synthesis |
| title_sort |
nitro compounds and their derivatives in organic synthesis |
| publisher |
MDPI - Multidisciplinary Digital Publishing Institute |
| publishDate |
2020 |
| physical |
1 electronic resource (120 p.) |
| isbn |
3-03943-148-X 3-03943-149-8 |
| illustrated |
Not Illustrated |
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AT nishiwakinagatoshi nitrocompoundsandtheirderivativesinorganicsynthesis |
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n |
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(CKB)5400000000042891 (oapen)https://directory.doabooks.org/handle/20.500.12854/69095 (EXLCZ)995400000000042891 |
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Nitro Compounds and Their Derivatives in Organic Synthesis |
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