Hayashi Minoru, Matsuura Yutaka, Watanabe Yutaka
Department of Materials Science and Biotechnology, Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama 790-8577, Japan.
J Org Chem. 2006 Nov 24;71(24):9248-51. doi: 10.1021/jo061739f.
A novel rhodium-catalyzed hydrophosphination of alkynes using a silylphosphine as a phosphino group source is described. A variety of alkynes, both terminal and internal ones with aryl, alkyl, and carboxyl groups, gave the corresponding alkenylphosphines in a highly regioselective and syn-selective manner. Alkenes with an electron-withdrawing group also gave the corresponding adducts in good yields.
描述了一种使用甲硅烷基膦作为膦基源的新型铑催化的炔烃氢膦化反应。各种炔烃,包括末端炔烃和带有芳基、烷基和羧基的内炔烃,都能以高度区域选择性和立体选择性的方式生成相应的烯基膦。带有吸电子基团的烯烃也能以良好的产率生成相应的加合物。