Fuji Kazuto, Kawashima Kyohei, Mori Toshifumi, Sekine Kohei, Kuninobu Yoichiro
Department of Interdisciplinary Engineering Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasugakoen, Kasuga-shi, Fukuoka 816-8580, Japan.
Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasugakoen, Kasuga-shi, Fukuoka 816-8580, Japan.
Org Lett. 2025 Feb 21;27(7):1614-1619. doi: 10.1021/acs.orglett.4c04694. Epub 2025 Feb 6.
This study demonstrates the rhodium-catalyzed divergent synthesis of 5-, 5,6-, and 8-membered silacyclic compounds, such as benzosilole, silolosiline, and disilocine, from (2-hydrosilylaryl)acetylenes. To achieve high product selectivity, intra- and intermolecular reactions are controlled by tuning the mono- and bidentate phosphine ligands on the rhodium catalyst precursor. Deuterium labeling experiments and computational studies reveal that the annulation reaction proceeds via hydride transfer to the alkyne moiety.
本研究展示了铑催化下由(2-氢硅基芳基)乙炔合成5元、5,6元及8元硅杂环化合物,如苯并硅杂环戊二烯、硅杂环戊硅氮烷和二硅杂环辛四烯的发散性合成方法。为实现高产物选择性,通过调节铑催化剂前体上的单齿和双齿膦配体来控制分子内和分子间反应。氘标记实验和计算研究表明,环化反应通过氢化物转移至炔烃部分进行。