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Rapid construction of multisubstituted olefin structures using vinylboronate ester platform leading to highly
Kenichiro Itami1, Keisuke Tonogaki, Youichi Ohashi
1Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan. itami@sbchem.kyoto-u.ac.jp
Abstract:
[reaction: see text] A catalytic one-pot triarylation on the C=C core of vinylboronate pinacol ester (1) produces extended pi-systems based on a multisubstituted olefin structure very rapidly. We established an efficient protocol for the Pd-catalyzed double C-H arylation of 1 with aryl halides, which was successfully integrated with C-B arylation with aryl halides (cross-coupling) in one pot. By using this method, several highly fluorescent materials with a wide range of color variations (blue to red) were discovered.
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