Issue 14, 2016

Palladium-catalyzed enantioselective allylic alkylation of trifluoromethyl group substituted racemic and acyclic unsymmetrical 1,3-disubstituted allylic esters with malonate anions

Abstract

We examined the palladium-catalyzed allylic alkylation of trifluoromethyl group-substituted racemic and acyclic unsymmetrical 1,3-disubstituted allylic benzoate with a malonate anion, and succeeded in obtaining an enantiomerically enriched product in high yields with high ee values through the dynamic kinetic asymmetric transformation (DYKAT). The best result was attained by the [Pd(C3H5)(cod)]BF4/(S)-tol-BINAP in the presence of BSA or DMAP as a base.

Graphical abstract: Palladium-catalyzed enantioselective allylic alkylation of trifluoromethyl group substituted racemic and acyclic unsymmetrical 1,3-disubstituted allylic esters with malonate anions

Supplementary files

Article information

Article type
Communication
Submitted
27 Feb 2016
Accepted
14 Mar 2016
First published
14 Mar 2016

Org. Biomol. Chem., 2016,14, 3501-3505

Palladium-catalyzed enantioselective allylic alkylation of trifluoromethyl group substituted racemic and acyclic unsymmetrical 1,3-disubstituted allylic esters with malonate anions

K. Ikeda, T. Futamura, T. Hanakawa, M. Minakawa and M. Kawatsura, Org. Biomol. Chem., 2016, 14, 3501 DOI: 10.1039/C6OB00449K

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