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

ABSTRACT: The asymmetric and catalytic Michael reaction between ?-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.

SUBMITTER: Martinez JI

PROVIDER: S-EPMC4685793 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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

Martínez Jose I JI Uria Uxue U Muñiz Maria M Reyes Efraím E Carrillo Luisa L Vicario Jose L JL

Beilstein journal of organic chemistry 20151214

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. ...[more]

PMID: 26734103

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