At Osaka University, a team of organic chemists has now developed and enhanced a chemical reaction that allows controlled transformations of one of the toughest chemical bonds.

“We previously developed a cobalt catalyzed Grignard reaction for making hindered quaternary carbon centers. But that reaction also showed potential for modifying carbon-fluorine bonds. We tried many different additives and eventually found one that let us selectively build the same quaternary carbon-carbon bonds at carbon-fluorine sites,” says first author Takanori Iwasaki.

The Grignard reaction is a classic reaction in organic chemistry, useful for building the carbon skeleton of molecules by transforming carbon-halogen bonds into carbon-carbon bonds. Fluorine is also considered to be a halogen but the carbon-fluorine bond is among the strongest known and is usually unreactive to Grignard chemistry. Performing any kind of chemical reaction at carbon-fluorine bonds is difficult without affecting the rest of the molecule.

The Osaka team enhanced their catalytic system for performing difficult Grignard chemistry at very crowded, so-called quaternary carbon atoms. By adding a carefully selected additive to this catalytic system, they boosted its ability to work selectively on carbon-fluorine bonds.

“We have shown that this reaction is a very useful tool for sequentially changing parts of a molecule with great control,” says Group leader, Nobuaki Kambe. “Our control over the chemistry of carbon-fluorine bonds should enable much more synthetic freedom for building complex carbon structures.”

Journal Reference:

1. Takanori Iwasaki, Koji Yamashita, Hitoshi Kuniyasu, Nobuaki Kambe. Co-Catalyzed Cross-Coupling Reaction of Alkyl Fluorides with Alkyl Grignard Reagents. Organic Letters, 2017; 19 (14): 3691 DOI: 10.1021/acs.orglett.7b01370

*Original article online at https://www.sciencedaily.com/releases/2017/07/170727102920.htm