Affiliation:
1. Institute of Industrial Science The University of Tokyo 4-6-1 Komaba Meguro-ku Tokyo 153–8505 Japan
Abstract
AbstractA decarboxylative condensation of malonic acid half thioesters (MAHTs) with aldehydes catalyzed by benzylammonium trifluoroacetate has been developed for the synthesis of (E)‐α,β‐unsaturated thioesters. The reaction of aromatic aldehydes and sterically non‐demanding aliphatic aldehydes proceeded smoothly at room temperature in DMF in a stereo‐ and regioselective manner. Besides the unsubstituted malonate, 2‐fluoro‐ and 2‐methylmalonates could be employed as a nucleophile. Use of the present catalyst could avoid nonproductive protiodecarboxylation of MAHTs.
Cited by
2 articles.
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