Beilstein Journal of Organic Chemistry (Dec 2015)

Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality

  • Jose I. Martínez,
  • Uxue Uria,
  • Maria Muñiz,
  • Efraím Reyes,
  • Luisa Carrillo,
  • Jose L. Vicario

DOI
https://doi.org/10.3762/bjoc.11.277
Journal volume & issue
Vol. 11, no. 1
pp. 2577 – 2583

Abstract

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The asymmetric and catalytic Michael reaction between α-nitroesters and nitroalkenes has been studied in the presence of two bifunctional catalysts both containing the same absolute chirality at the carbon backbone. The reaction performed in similar conditions allows us to control the syn or anti selectivity of the Michael adduct obtaining good yields and high enantiocontrol in all cases.

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