Issue 42, 2016

Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids

Abstract

A new type of di-site chiral phase transfer catalyst has been designed and synthesized from cinchona alkaloids as a chiral precursor. The prepared catalysts are applied in the asymmetric Henry reaction to a wide range of aldehydes using mild concentrations of a base and solvent and under room-temperature conditions. Under the optimized reaction conditions, the highest chemical yields up to 99% along with an excellent enantiomeric excess (ee) up to 99% were obtained using the prepared cinchona alkaloid based chiral phase transfer catalysts.

Graphical abstract: Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids

Supplementary files

Article information

Article type
Paper
Submitted
05 Aug 2016
Accepted
01 Oct 2016
First published
04 Oct 2016

Org. Biomol. Chem., 2016,14, 10101-10109

Highly enantioselective asymmetric Henry reaction catalyzed by novel chiral phase transfer catalysts derived from cinchona alkaloids

P. K. Vijaya, S. Murugesan and A. Siva, Org. Biomol. Chem., 2016, 14, 10101 DOI: 10.1039/C6OB01687A

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