Affiliation:
1. Department of Chemistry Graduate School of Science Kyoto University Sakyo-ku Kyoto 606-8502 Japan
2. Department of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
3. Future correspondence: School of Chemistry University of Southampton Southampton SO17 1BJ UK
Abstract
AbstractThe potassium salts of carboxylic acids are developed as efficient carboxylating agents through CO2 exchange. We describe these carboxylates as dual‐function reagents because they function as a combined source of CO2 and base/metalating agent. By using the salt of a commercially available carboxylic acid, this protocol overcomes difficulties when using CO2 gas or organometallic reagents, such as pressurized containers or strictly inert conditions. The reaction proceeds under mild conditions, does not require transition metals or other additives, and shows broad substrate scope. Through the preparation of several biologically important molecules, we show how this strategy provides an opportunity for isotope labeling with low equivalents of labeled CO2.
Funder
Royal Society
Japan Society for the Promotion of Science
Core Research for Evolutional Science and Technology
Subject
General Chemistry,Catalysis
Cited by
2 articles.
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