Saito Kenta, Chikkade Prasanna Kumara, Kanai Motomu, Kuninobu Yoichiro
Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan).
ERATO (Japan) Science and Technology Agency (JST), Kanai Life Science Catalysis Project, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan).
Chemistry. 2015 Jun 1;21(23):8365-8. doi: 10.1002/chem.201501116. Epub 2015 Apr 23.
Synthesis of heteroatom-containing ladder-type π-conjugated molecules was successfully achieved via a palladium-catalyzed intramolecular oxidative C-H/C-H cross-coupling reaction. This reaction provides a variety of π-conjugated molecules bearing heteroatoms, such as nitrogen, oxygen, phosphorus, and sulfur atoms, and a carbonyl group. The π-conjugated molecules were synthesized efficiently, even in gram scale, and larger π-conjugated molecules were also obtained by a double C-H/C-H cross-coupling reaction and successive oxidative cycloaromatization.
通过钯催化的分子内氧化C-H/C-H交叉偶联反应成功实现了含杂原子的梯形π共轭分子的合成。该反应提供了多种带有杂原子(如氮、氧、磷和硫原子)以及羰基的π共轭分子。即使在克级规模下,π共轭分子也能高效合成,并且通过双C-H/C-H交叉偶联反应和连续氧化环化反应还能得到更大的π共轭分子。