Letters in Organic Chemistry

Author(s): M. Molteni and ">M. Zanda

DOI: 10.2174/1570178054640769

Functionalized, Differently Fluorinated Building-Blocks Via Michael Addition of Enamines to γ-Fluoro-α-Nitroalkenes

Page: [566 - 568] Pages: 3

  • * (Excluding Mailing and Handling)

Abstract

The Michael addition of ketone-derived enamines to γ-fluoro-α-nitroalkenes provides in moderate to good isolated yields the corresponding β-fluoroalkyl γ-nitroketones, which can be reduced to β-fluoroalkyl γ- nitroalcohols.

Keywords: nitroalkenes, fluorinated building blocks, michael addition, diels-alder, dipolar reactions, (nitroaldol) reaction, tbaf, mukaiyama-like conditions