Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis?
Because of improved methods for the conversion of nitroaliphatics into amines, alcohols, and carbonyl compounds, carbon-carbon bond forming processes involving this class of substrate are of increasing importance. This article reviews the work of ourselves and others, and demonstrates that nitroali...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1979-01-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9430 |
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| _version_ | 1849311262165434368 |
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| author | Dieter Seebach Ernest W. Colvin Friedrich Lehr Thomas Weller |
| author_facet | Dieter Seebach Ernest W. Colvin Friedrich Lehr Thomas Weller |
| author_sort | Dieter Seebach |
| collection | DOAJ |
| description |
Because of improved methods for the conversion of nitroaliphatics into amines, alcohols, and carbonyl compounds, carbon-carbon bond forming processes involving this class of substrate are of increasing importance. This article reviews the work of ourselves and others, and demonstrates that nitroaliphatic compounds can show either electrophilic or nucleophilic reactivity at the α-, β-, γ-, and δ-positions.
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| format | Article |
| id | doaj-art-b6ec9c64e2fc4879bc93826ffcc6e4b4 |
| institution | Kabale University |
| issn | 0009-4293 2673-2424 |
| language | deu |
| publishDate | 1979-01-01 |
| publisher | Swiss Chemical Society |
| record_format | Article |
| series | CHIMIA |
| spelling | doaj-art-b6ec9c64e2fc4879bc93826ffcc6e4b42025-08-20T03:53:27ZdeuSwiss Chemical SocietyCHIMIA0009-42932673-24241979-01-0133110.2533/chimia.1979.1Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis?Dieter Seebach0Ernest W. Colvin1Friedrich Lehr2Thomas Weller3Laboratorium für Organische Chemie, ETH ZürichLaboratorium für Organische Chemie, ETH ZürichLaboratorium für Organische Chemie, ETH ZürichLaboratorium für Organische Chemie, ETH Zürich Because of improved methods for the conversion of nitroaliphatics into amines, alcohols, and carbonyl compounds, carbon-carbon bond forming processes involving this class of substrate are of increasing importance. This article reviews the work of ourselves and others, and demonstrates that nitroaliphatic compounds can show either electrophilic or nucleophilic reactivity at the α-, β-, γ-, and δ-positions. https://www.chimia.ch/chimia/article/view/9430 |
| spellingShingle | Dieter Seebach Ernest W. Colvin Friedrich Lehr Thomas Weller Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? CHIMIA |
| title | Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? |
| title_full | Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? |
| title_fullStr | Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? |
| title_full_unstemmed | Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? |
| title_short | Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis? |
| title_sort | nitroaliphatic compounds ideal intermediates in organic synthesis |
| url | https://www.chimia.ch/chimia/article/view/9430 |
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