Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis?

Authors

  • Dieter Seebach Laboratorium für Organische Chemie, ETH Zürich
  • Ernest W. Colvin Laboratorium für Organische Chemie, ETH Zürich
  • Friedrich Lehr Laboratorium für Organische Chemie, ETH Zürich
  • Thomas Weller Laboratorium für Organische Chemie, ETH Zürich

DOI:

https://doi.org/10.2533/chimia.1979.1

Abstract

Because of improved methods for the conversion of nitroali-phatics 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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Published

1979-01-31

How to Cite

[1]
D. Seebach, E. W. Colvin, F. Lehr, T. Weller, Chimia 1979, 33, 1, DOI: 10.2533/chimia.1979.1.