Department of Chemistry, Tokyo Institute of Technology and CREST-JST, O-okayama, Meguro-ku, Tokyo 152-8551, Japan.
J Am Chem Soc. 2011 Aug 24;133(33):12980-3. doi: 10.1021/ja205186k. Epub 2011 Aug 2.
The efficient synthesis of various diborylalkenes such as 1,1-, trans-1,2-, and cyclic 1,2-diborylalkenes from alkenes and diboron was achieved for the first time. Selective preparation of di- and monoborylalkenes was also realized by the appropriate choice of reaction conditions. The reaction was found to proceed via a new mechanism of dehydrogenative borylation through a monoborylpalladium complex bearing an anionic PSiP-pincer ligand as a key intermediate, which realized the efficient borylation without sacrificial hydroboration or hydrogenation of the alkene.
首次实现了从烯烃和二硼出发高效合成各种二硼烯,如 1,1-、反式-1,2-和环状 1,2-二硼烯。通过适当选择反应条件,还实现了二硼烯和单硼烯的选择性制备。该反应被发现通过一种新型的脱氢硼化反应机理进行,其中一个关键中间体是带有阴离子 PSiP-夹式配体的单硼钯配合物,该中间体实现了高效硼化,而无需牺牲烯烃的硼氢化或加氢。