Affiliation:
1. Department of Applied Chemistry and Life Science Toyohashi University of Technology 1-1 Hibarigaoka, Tempaku-cho Toyohashi 441-8580 Japan
Abstract
AbstractSyntheses of substituted pyridines and fluorinated compounds, which are often pharmaceutical targets, are important objectives in organic chemistry. Herein, we found that decarboxylative fluorination of lithium 2‐pyridylacetates occur under catalyst‐free conditions. The phenomenon can be applied to one‐pot transformation of substituted methyl 2‐pyridylacetate to 2‐(fluoroalkyl)pyridine by decarboxylative fluorination of the intermediate lithium 2‐pyridylacetate. This method was also applied to the syntheses of 2‐(difluoroalkyl)pyridines.
Funder
Japan Society for the Promotion of Science
Cited by
17 articles.
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